RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (14 ms elapsed)

{
  "NDC": [
    {
      "NDCCode": "27281-008-96",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-008-96)",
      "NDC11Code": "27281-0008-96",
      "ProductNDC": "27281-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Heartery",
      "NonProprietaryName": "American Ginseng, Arnica Montana, Gold, Barium Carbonate, Atropa Belladonna, Calcium Fluoride, Cholesterol, Herring Sperm Dna, Ginkgo, Saccharomyces Cerevisia Rna, Visbum Album Fruiting Top, And Ginger",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131209",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "AMERICAN GINSENG; ARNICA MONTANA; GOLD; BARIUM CARBONATE; ATROPA BELLADONNA; CALCIUM FLUORIDE; CHOLESTEROL; HERRING SPERM DNA; GINKGO; SACCHAROMYCES CEREVISIAE RNA; VISCUM ALBUM FRUITING TOP; GINGER",
      "StrengthNumber": "1; 1.5; 30; 30; 3; 6; 15; 3; 3; 3; 1.5; 30",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves symptoms associated with hypertension, such as: high blood pressure; constricted blood vessels; arteriosclerosis; inelastic blood vessels."
    },
    {
      "NDCCode": "27281-001-96",
      "PackageDescription": "30 mL in 1 PACKAGE (27281-001-96)",
      "NDC11Code": "27281-0001-96",
      "ProductNDC": "27281-001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Brain Power",
      "NonProprietaryName": "Semecarpus Anacardium Juice, Arnica Montana, Calcium Fluoride, Silybum Marianum Seed, Chincona Officinalis Bark, Herring Sperm Dna, Ginkgo, Egg Phospholipids, Achillea Millefolium, Phosphoric Acid, Saccharomyces Cerevisia Rna, Silicon Dioxide, And Zinc Sulphate Heptahydrate",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131118",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "SEMECARPUS ANACARDIUM JUICE; ARNICA MONTANA; CALCIUM FLUORIDE; SILYBUM MARIANUM SEED OIL; CINCHONA OFFICINALIS BARK; HERRING SPERM DNA; GINKGO; EGG PHOSPHOLIPIDS; ACHILLEA MILLEFOLIUM; PHOSPHORIC ACID; SACCHAROMYCES CEREVISIAE RNA; SILICON DIOXIDE; ZINC SULFATE HEPTAHYDRATE",
      "StrengthNumber": "30; 1.5; 30; 1.5; 3; 3; 3; 6; 1.5; 30; 6; 6; 6",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves symptoms of mental fatigue, including: lapses in memory; feelings of confusion or difficulty collecting one's thoughts; short attention span; poor mood."
    },
    {
      "NDCCode": "27281-002-96",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-002-96)",
      "NDC11Code": "27281-0002-96",
      "ProductNDC": "27281-002",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Livergen",
      "NonProprietaryName": "Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ARNICA MONTANA; BRYONIA ALBA ROOT; SILYBUM MARIANUM SEED OIL; CHELIDONIUM MAJUS; HERRING SPERM DNA; PORK LIVER; CERVUS ELAPHUS HORN OIL; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE",
      "StrengthNumber": "1.5; 200; .5; 200; 3; 3; 4; 4; 1",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Helps detoxify the liver and temporarily relieves symptoms associated with an overworked or toxic liver, including: fatigue; poor sugar metabolism; poor liver function; ill effects of excessive alcohol consumption."
    },
    {
      "NDCCode": "27281-004-96",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-004-96)",
      "NDC11Code": "27281-0004-96",
      "ProductNDC": "27281-004",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Immune Booster",
      "NonProprietaryName": "Apis Mellifera, Baptisia Tinctoria, Silybum Marianum Seed, Herring Sperm Dna, Echinacea, Galium Aparine, Mercuric Chloride, Mercuric Sulfide, Nitric Acid, Sulfur Iodide, And Thuja Occidentalis Leafy Twig",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "APIS MELLIFERA; BAPTISIA TINCTORIA; SILYBUM MARIANUM SEED OIL; HERRING SPERM DNA; ECHINACEA, UNSPECIFIED; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "200; 3; 1.5; 3; 3; 1.5; 200; 30; 30; 200; 200",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Helps support the body's natural defense mechanisms and temporarily relieves: tendencies toward flu & cold; joint pain; minor allergies; low endocrine function."
    },
    {
      "NDCCode": "27281-007-96",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-007-96)",
      "NDC11Code": "27281-0007-96",
      "ProductNDC": "27281-007",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Diabetigen",
      "NonProprietaryName": "Arnica Montana, Arsenic Trioxide, Herring Sperm Nda, Echinacea, Unspecified, Hamamelis Virginiana Leaf, Chamaelirium Luteum Root, Pork Liver, Iris Versicolor Root, Sus Scrofa Pancreas, Phosphoric Acid, Rosmarinus Officinalis Flowering Top, Claviceps Purpurea Sclerotium, Syzygium Cumini Seed, And Uranyl Nitrate Hexahydrate",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131209",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ARNICA MONTANA; ARSENIC TRIOXIDE; HERRING SPERM DNA; ECHINACEA, UNSPECIFIED; HAMAMELIS VIRGINIANA LEAF; CHAMAELIRIUM LUTEUM ROOT; PORK LIVER; IRIS VERSICOLOR ROOT; SUS SCROFA PANCREAS; PHOSPHORIC ACID; ROSMARINUS OFFICINALIS FLOWERING TOP; CLAVICEPS PURPUREA SCLEROTIUM; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE",
      "StrengthNumber": "1.5; 200; 3; 1.5; 1.5; 1.5; 3; 3; 3; 200; 1.5; 30; 1.5; 30",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications:  Temporarily relieves symptoms associated with type II diabetes, including: pancreatic deficiency; liver weakness; apathy and generalized feelings of weakness."
    },
    {
      "NDCCode": "27281-009-96",
      "PackageDescription": "30 mg in 1 BOTTLE, SPRAY (27281-009-96)",
      "NDC11Code": "27281-0009-96",
      "ProductNDC": "27281-009",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Female Energy",
      "NonProprietaryName": "Chaste Tree, Arnica Montana, Caulophyllum Thalictroides Root, Cinchona Officinalis Bark, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Lactuca Virosa, Onosmodium Virginianum Whole, Sus Scrofa Ovary, Phosphoric Acid, Sus Scrofa Pituitary Gland, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140807",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "CHASTE TREE; ARNICA MONTANA; CAULOPHYLLUM THALICTROIDES ROOT; CINCHONA OFFICINALIS BARK; TURNERA DIFFUSA LEAFY TWIG; HERRING SPERM DNA; LACTUCA VIROSA; ONOSMODIUM VIRGINIANUM WHOLE; SUS SCROFA OVARY; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "1.5; 1.5; 3; 1.5; .5; 3; 1.5; 30; 30; 200; 6; 30; 30",
      "StrengthUnit": "[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves some symptoms of low female sexual energy, such as: decrease in sexual desire; feelings of fatigue; decrease in responsiveness and enjoyment."
    },
    {
      "NDCCode": "27281-010-96",
      "PackageDescription": "30 mg in 1 BOTTLE, SPRAY (27281-010-96)",
      "NDC11Code": "27281-0010-96",
      "ProductNDC": "27281-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Male Tonicity",
      "NonProprietaryName": "American Ginseng, Arnica Montana, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Galium Aparine, Hamamelis Virginiana Root Bark/stem Bark, Pork Liver, Cervus Elaphus Horn Oil, Ovis Aries Testicle, Phosphoric Acid, Sus Scrofa Pituitary Gland, Thuja Occidentalis Leafy Twig, Thyroid, Unspecified, Tribulus Terrestris, Ginger",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140808",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "AMERICAN GINSENG; ARNICA MONTANA; TURNERA DIFFUSA LEAFY TWIG; HERRING SPERM DNA; GALIUM APARINE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PORK LIVER; CERVUS ELAPHUS HORN OIL; OVIS ARIES TESTICLE; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, UNSPECIFIED; TRIBULUS TERRESTRIS; GINGER",
      "StrengthNumber": "1.5; 1.5; 1; 3; 1.5; 1.5; 3; 4; 3; 200; 4; 1.5; 6; 1; 1.5",
      "StrengthUnit": "[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves symptoms of low male sexual energy, including: decrease in sexual desire; feelings of fatigue; decrease in performance and enjoyment."
    },
    {
      "NDCCode": "27281-011-96",
      "PackageDescription": "30 mg in 1 BOTTLE, SPRAY (27281-011-96)",
      "NDC11Code": "27281-0011-96",
      "ProductNDC": "27281-011",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Lung Detox",
      "NonProprietaryName": "Silver Nitrate, Arsenic Trioxide, Activated Charcoal, Silybum Marianum Seed, Herring Sperm Dna, Pork Liver, Mercuric Chloride, Lead",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140808",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "SILVER NITRATE; ARSENIC TRIOXIDE; ACTIVATED CHARCOAL; SILYBUM MARIANUM SEED; HERRING SPERM DNA; PORK LIVER; MERCURIC CHLORIDE; LEAD",
      "StrengthNumber": "200; 200; 200; .5; 3; 3; 200; 200",
      "StrengthUnit": "[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Detoxifies the lungs and provides temporary relief from symtpoms associated with inhaling polluted air, both indoors and outdoors, such as: shortness of breath; wheezing; coughing; lack of energy."
    },
    {
      "NDCCode": "54273-008-01",
      "PackageDescription": "96 g in 1 CAN (54273-008-01) ",
      "NDC11Code": "54273-0008-01",
      "ProductNDC": "54273-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Zims Max Freeze",
      "ProprietaryNameSuffix": "Pro Formula",
      "NonProprietaryName": "Menthol",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20180924",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M017",
      "LabelerName": "KOBAYASHI Healthcare International, Inc.",
      "SubstanceName": "MENTHOL, UNSPECIFIED FORM",
      "StrengthNumber": "160",
      "StrengthUnit": "mg/g",
      "Status": "Active",
      "LastUpdate": "2023-11-18",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20180924",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor aches and pains of muscles and joints associated with: 1 Simple backache, 2 Arthritis, 3 Strains, 4 Bruises, 5 Sprains."
    },
    {
      "NDCCode": "54641-008-01",
      "PackageDescription": "96 g in 1 CONTAINER (54641-008-01) ",
      "NDC11Code": "54641-0008-01",
      "ProductNDC": "54641-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Flex24 Pain",
      "NonProprietaryName": "Camphor Menthol",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20190222",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "Larasan Pharmaceutical Corporation",
      "SubstanceName": "CAMPHOR (NATURAL); MENTHOL",
      "StrengthNumber": "3; 10",
      "StrengthUnit": "1/100g; g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2021-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20190222",
      "SamplePackage": "N",
      "IndicationAndUsage": "For temporary relief of minor aches and pains of muscle and joints associated with simple backache, arthritis, strains, cramps, bruises, and sprains."
    },
    {
      "NDCCode": "71481-008-01",
      "PackageDescription": "96 TABLET in 1 BOTTLE (71481-008-01) ",
      "NDC11Code": "71481-0008-01",
      "ProductNDC": "71481-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bio V Antacid Berry 96ct",
      "NonProprietaryName": "Calcium Carbonate",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20220228",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M001",
      "LabelerName": "BioV Health Inc",
      "SubstanceName": "CALCIUM CARBONATE",
      "StrengthNumber": "750",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2025-07-30",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20220228",
      "SamplePackage": "N",
      "IndicationAndUsage": "Relieves  acid indigestion  heartburn  sour stomach  upset stomach associated with these symptoms."
    },
    {
      "NDCCode": "72351-008-00",
      "PackageDescription": "96 GEL in 1 PACKAGE (72351-008-00) ",
      "NDC11Code": "72351-0008-00",
      "ProductNDC": "72351-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Rite Aid Roll-on",
      "NonProprietaryName": "Menthol",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20180809",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "SOTAC PHARMACEUTICALS PRIVATE LIMITED",
      "SubstanceName": "MENTHOL",
      "StrengthNumber": "40",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20180809",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporary relief from minor aches and pains of sore muscles and joints associated with:  - arthritis, - backache,  - strains, - sprains."
    },
    {
      "NDCCode": "72476-008-96",
      "PackageDescription": "221 mL in 1 BOTTLE, PUMP (72476-008-96) ",
      "NDC11Code": "72476-0008-96",
      "ProductNDC": "72476-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Hand Wash",
      "NonProprietaryName": "Benzalkonium Chloride",
      "DosageFormName": "SOAP",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20141002",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part333A",
      "LabelerName": "RETAIL BUSINESS SERVICES , LLC",
      "SubstanceName": "BENZALKONIUM CHLORIDE",
      "StrengthNumber": "1.3",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2023-09-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20231231",
      "StartMarketingDatePackage": "20141002",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "10631-008-30",
      "PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-008-30) ",
      "NDC11Code": "10631-0008-30",
      "ProductNDC": "10631-008",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Kapspargo",
      "NonProprietaryName": "Metoprolol Succinate",
      "DosageFormName": "CAPSULE, EXTENDED RELEASE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20180315",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA210428",
      "LabelerName": "Sun Pharmaceutical Industries, Inc.",
      "SubstanceName": "METOPROLOL SUCCINATE",
      "StrengthNumber": "25",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
      "Status": "Active",
      "LastUpdate": "2023-04-20",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20180315",
      "SamplePackage": "N",
      "IndicationAndUsage": "KAPSPARGO Sprinkle is a beta1-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) Angina Pectoris. (1.2) Heart Failure, to reduce the risk of cardiovascular mortality and heart-failure hospitalizations in patients with heart failure. (1.3).",
      "Description": "Metoprolol succinate, is a beta1-selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release capsules. Metoprolol succinate extended-release capsules have been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The extended-release capsules comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets. Each pellet acts as a separate drug delivery unit and is designed to deliver metoprolol continuously over the dosage interval. The extended-release capsules contain 10.24 mg, 20.48 mg, 40.96 mg, and 81.92 mg of metoprolol free base, present as 23.75 mg, 47.5 mg, 95 mg, and 190 mg of metoprolol succinate and are equivalent to 25 mg, 50 mg, 100 mg, and 200 mg of metoprolol tartrate, USP, respectively. Its chemical name is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)phenoxy]-2-propanol succinate (2:1) (salt). Its structural formula is. Metoprolol succinate, USP is a white to off-white powder with a molecular weight of 652.82. It is freely soluble in water, soluble in methanol, sparingly soluble in alcohol, slightly soluble in isopropyl alcohol. Inactive ingredients: ethyl cellulose, hypromellose, polyethylene glycol 400, polyethylene glycol 6000, sugar spheres (corn starch and sucrose), talc and triethyl citrate. The capsule shell and imprinting ink has the following composition: ferric oxide yellow (25 mg, 50 mg and 200 mg), ferrosoferric oxide, gelatin, potassium hydroxide, propylene glycol, shellac and titanium dioxide."
    },
    {
      "NDCCode": "49967-008-01",
      "PackageDescription": "143 g in 1 BOTTLE, SPRAY (49967-008-01) ",
      "NDC11Code": "49967-0008-01",
      "ProductNDC": "49967-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Broad Spectrum Spf 60 Water Resistant 80 Minutes",
      "NonProprietaryName": "Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20140101",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M020",
      "LabelerName": "L'Oreal USA Products Inc",
      "SubstanceName": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE",
      "StrengthNumber": "26.8; 96; 28.8; 53.8; 34.6",
      "StrengthUnit": "mg/g; mg/g; mg/g; mg/g; mg/g",
      "Status": "Active",
      "LastUpdate": "2024-01-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20140101",
      "SamplePackage": "N",
      "IndicationAndUsage": "helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun."
    },
    {
      "NDCCode": "52720-008-01",
      "PackageDescription": "8 mL in 1 VIAL (52720-008-01) ",
      "NDC11Code": "52720-0008-01",
      "ProductNDC": "52720-008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Ariel Premium Supply Hand Sanitizer",
      "NonProprietaryName": "Hand Sanitizer",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20200820",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part333E",
      "LabelerName": "ZHONGSHAN S. JANE BIOTECHNOLOGY CO., LTD.",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "4.96",
      "StrengthUnit": "mL/8mL",
      "Status": "Deprecated",
      "LastUpdate": "2021-02-19",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20200820",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "63304-008-30",
      "PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-008-30) ",
      "NDC11Code": "63304-0008-30",
      "ProductNDC": "63304-008",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Metoprolol Succinate",
      "NonProprietaryName": "Metoprolol Succinate",
      "DosageFormName": "CAPSULE, EXTENDED RELEASE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20180207",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA210428",
      "LabelerName": "Sun Pharmaceutical Industries Inc.",
      "SubstanceName": "METOPROLOL SUCCINATE",
      "StrengthNumber": "25",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
      "Status": "Active",
      "LastUpdate": "2018-02-09",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20180207",
      "SamplePackage": "N",
      "IndicationAndUsage": "Metoprolol succinate extended-release capsules are beta1-selective adrenoceptor blocking agent indicated for the treatment of: : 1 Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) , 2 Angina Pectoris. (1.2) , 3 Heart Failure, to reduce the risk of cardiovascular mortality and heart-failure hospitalization in patients with heart failure. (1.3).",
      "Description": "Metoprolol succinate, is a beta1-selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release capsules. Metoprolol succinate extended-release capsules have been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The extended-release capsules comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets. Each pellet acts as a separate drug delivery unit and is designed to deliver metoprolol continuously over the dosage interval. The extended-release capsules contain 10.24 mg, 20.48 mg, 40.96 mg, and 81.92 mg of metoprolol free base, present as 23.75 mg, 47.5 mg, 95 mg, and 190 mg of metoprolol succinate and are equivalent to 25 mg, 50 mg, 100 mg, and 200 mg of metoprolol tartrate, USP, respectively. Its chemical name is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)phenoxy]-2-propanol succinate (2:1) (salt). Its structural formula is. Metoprolol succinate, USP is a white to off-white powder with a molecular weight of 652.82. It is freely soluble in water, soluble in methanol, sparingly soluble in alcohol, slightly soluble in isopropyl alcohol. Inactive ingredients: ethyl cellulose, hypromellose, polyethylene glycol 400, polyethylene glycol 6000, sugar spheres (corn starch and sucrose), talc and triethyl citrate. The capsule shell and imprinting ink has the following composition: ferric oxide yellow (25 mg, 50 mg and 200 mg), ferrosoferric oxide, gelatin, potassium hydroxide, propylene glycol, shellac and titanium dioxide."
    },
    {
      "NDCCode": "73159-008-60",
      "PackageDescription": "1 BOTTLE in 1 CARTON (73159-008-60)  / 59 g in 1 BOTTLE",
      "NDC11Code": "73159-0008-60",
      "ProductNDC": "73159-008",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Ultravate",
      "NonProprietaryName": "Halobetasol Propionate",
      "DosageFormName": "LOTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20250406",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA208183",
      "LabelerName": "Lacer Pharma, LLC",
      "SubstanceName": "HALOBETASOL PROPIONATE",
      "StrengthNumber": ".5",
      "StrengthUnit": "mg/g",
      "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
      "Status": "Active",
      "LastUpdate": "2025-05-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20250406",
      "SamplePackage": "N",
      "IndicationAndUsage": "ULTRAVATE lotion is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.",
      "Description": "ULTRAVATE (halobetasol propionate) lotion, 0.05% for topical use contains a corticosteroid, halobetasol propionate. The chemical name of halobetasol propionate is 21­ chloro-6α, 9-difluoro-11β, 17-dihydroxy-16β-methylpregna-1, 4-diene-3,20-dione 17­ propionate. Halobetasol propionate is a white to off-white crystalline powder with a molecular weight of 484.96 and a molecular formula of C 25H 31ClF 2O 5. It is practically insoluble in water and freely soluble in dichloromethane and in acetone. It has the following structural formula:. Each gram of ULTRAVATE lotion contains 0.5 mg of halobetasol propionate in a white to off-white lotion base consisting of diisopropyl adipate, octyldodecanol, ceteth-20, poloxamer 407, cetyl alcohol, stearyl alcohol, propylparaben, butylparaben, propylene glycol, glycerin, carbomer homopolymer, sodium hydroxide, and water."
    },
    {
      "NDCCode": "85437-008-60",
      "PackageDescription": "1 BOTTLE in 1 CARTON (85437-008-60)  / 59 g in 1 BOTTLE",
      "NDC11Code": "85437-0008-60",
      "ProductNDC": "85437-008",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Halobetasol Propionate",
      "NonProprietaryName": "Halobetasol Propionate",
      "DosageFormName": "LOTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20260310",
      "EndMarketingDate": "20270531",
      "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
      "ApplicationNumber": "NDA208183",
      "LabelerName": "Coral Way Pharma, LLC",
      "SubstanceName": "HALOBETASOL PROPIONATE",
      "StrengthNumber": ".5",
      "StrengthUnit": "mg/g",
      "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
      "Status": "Active",
      "LastUpdate": "2026-07-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20260310",
      "EndMarketingDatePackage": "20270531",
      "SamplePackage": "N",
      "IndicationAndUsage": "Halobetasol Propionate Lotion 0.05% is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.",
      "Description": "Halobetasol Propionate Lotion 0.05% for topical use contains a corticosteroid, halobetasol propionate. The chemical name of halobetasol propionate is 21­ chloro-6α, 9-difluoro-11β, 17-dihydroxy-16β-methylpregna-1, 4-diene-3,20-dione 17­ propionate. Halobetasol propionate is a white to off-white crystalline powder with a molecular weight of 484.96 and a molecular formula of C 25H 31ClF 2O 5. It is practically insoluble in water and freely soluble in dichloromethane and in acetone. It has the following structural formula:. Each gram of Halobetasol Propionate Lotion 0.05% contains 0.5 mg of halobetasol propionate in a white to off-white lotion base consisting of diisopropyl adipate, octyldodecanol, ceteth-20, poloxamer 407, cetyl alcohol, stearyl alcohol, propylparaben, butylparaben, propylene glycol, glycerin, carbomer homopolymer, sodium hydroxide, and water."
    },
    {
      "NDCCode": "27281-003-01",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-003-01)",
      "NDC11Code": "27281-0003-01",
      "ProductNDC": "27281-003",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Vivacity",
      "NonProprietaryName": "Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ALFALFA; ARNICA MONTANA; AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; HERRING SPERM DNA; HYPERICUM PERFORATUM; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "1; 1.5; 1; 1; 1.5; 3; 200; 3; 4; 200; 3; 30",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves symptoms of general physical weakness and listlessness, including: fatigue; sore muscles & joints; dry skin; absence of sexual desire; occasional sleeplessness."
    },
    {
      "NDCCode": "27281-003-02",
      "PackageDescription": "60 mL in 1 BOTTLE, SPRAY (27281-003-02)",
      "NDC11Code": "27281-0003-02",
      "ProductNDC": "27281-003",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Vivacity",
      "NonProprietaryName": "Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water",
      "DosageFormName": "SPRAY",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ALFALFA; ARNICA MONTANA; AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; HERRING SPERM DNA; HYPERICUM PERFORATUM; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "1; 1.5; 1; 1; 1.5; 3; 200; 3; 4; 200; 3; 30",
      "StrengthUnit": "[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Indications: Temporarily relieves symptoms of general physical weakness and listlessness, including: fatigue; sore muscles & joints; dry skin; absence of sexual desire; occasional sleeplessness."
    },
    {
      "NDCCode": "27281-029-63",
      "PackageDescription": "30 mL in 1 PACKAGE (27281-029-63) ",
      "NDC11Code": "27281-0029-63",
      "ProductNDC": "27281-029",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Livergen",
      "NonProprietaryName": "Arnica Montana, Bryonia, Carduus Marianus, Chelidonium Majus, Dna, Hepar Suis, Oleum Animale, Pancreas Suis, Taraxacum Officinale.",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ARNICA MONTANA; BRYONIA ALBA ROOT; MILK THISTLE; CHELIDONIUM MAJUS; HERRING SPERM DNA; PORK LIVER; CERVUS ELAPHUS HORN OIL; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE",
      "StrengthNumber": "3; 200; 1; 200; 6; 6; 8; 8; 2",
      "StrengthUnit": "[hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL",
      "Status": "Active",
      "LastUpdate": "2021-12-31",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20131113",
      "SamplePackage": "N",
      "IndicationAndUsage": "​USES: ​Relieves symptoms of aging or a rundown condition, including: Relief for feelings of fatigue that may be caused by an over-worked liver or by liver toxixity; supports proper sugar metabolism; stimulates proper liver function; protects against the ill-effects of excessive alcohol consumption.*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated."
    },
    {
      "NDCCode": "27281-039-64",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-039-64) ",
      "NDC11Code": "27281-0039-64",
      "ProductNDC": "27281-039",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Vivacity",
      "NonProprietaryName": "Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, Rna, Thuja Occidentalis",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20180205",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "ALFALFA; ARNICA MONTANA; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; PORK LIVER; HYPERICUM PERFORATUM; ASIAN GINSENG; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "2; 3; 2; 3; 6; 200; 2; 6; 8; 200; 6; 30",
      "StrengthUnit": "[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL",
      "Status": "Active",
      "LastUpdate": "2021-12-31",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20180205",
      "SamplePackage": "N",
      "IndicationAndUsage": "​USES: ​Relieves symptoms of aging or a rundown condition, including: Low energy; poor muscle balance; poor stamina; occssional sleeplessnees.*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated."
    },
    {
      "NDCCode": "27281-049-65",
      "PackageDescription": "30 mL in 1 BOTTLE, SPRAY (27281-049-65) ",
      "NDC11Code": "27281-0049-65",
      "ProductNDC": "27281-049",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Immune Booster",
      "NonProprietaryName": "Apis Mellifica, Baptisia Tinctoria, Carduus Marianus, Echinacea Angustifolia, Gallum Aparine, Mercurius Corrosivus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Sulphur Iodatum, Thuja Occidentalis.",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131113",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Sunway Biotech LLC",
      "SubstanceName": "APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; MILK THISTLE; ECHINACEA ANGUSTIFOLIA; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "200; 6; 3; 6; 3; 200; 30; 30; 200; 200",
      "StrengthUnit": "[hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL",
      "Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]",
      "Status": "Active",
      "LastUpdate": "2021-12-31",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20131113",
      "SamplePackage": "N",
      "IndicationAndUsage": "​USES: ​Supports the body's natural defense mechanisms, temporarily relieves: tendency towards flu & cold; joint pain; minor allergy. Helps balance the body's level of Human Growth Hormone, supporting healthy immune response. Stimulates the endocrine glands*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated."
    },
    {
      "NDCCode": "0003-3734-13",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3734-13)  / 24 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00003-3734-13",
      "ProductNDC": "0003-3734",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Opdivo",
      "NonProprietaryName": "Nivolumab",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20171208",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125554",
      "LabelerName": "E.R. Squibb & Sons, L.L.C.",
      "SubstanceName": "NIVOLUMAB",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-08-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20171208",
      "SamplePackage": "N",
      "IndicationAndUsage": "OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).",
      "Description": "Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6."
    },
    {
      "NDCCode": "0003-3756-14",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3756-14)  / 12 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00003-3756-14",
      "ProductNDC": "0003-3756",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Opdivo",
      "NonProprietaryName": "Nivolumab",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20210830",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125554",
      "LabelerName": "E.R. Squibb & Sons, L.L.C.",
      "SubstanceName": "NIVOLUMAB",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-08-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20210830",
      "SamplePackage": "N",
      "IndicationAndUsage": "OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).",
      "Description": "Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6."
    },
    {
      "NDCCode": "0003-3772-11",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3772-11)  / 4 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00003-3772-11",
      "ProductNDC": "0003-3772",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Opdivo",
      "NonProprietaryName": "Nivolumab",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20141222",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125554",
      "LabelerName": "E.R. Squibb & Sons, L.L.C.",
      "SubstanceName": "NIVOLUMAB",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-08-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20141222",
      "SamplePackage": "N",
      "IndicationAndUsage": "OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).",
      "Description": "Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6."
    },
    {
      "NDCCode": "0003-3774-12",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3774-12)  / 10 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00003-3774-12",
      "ProductNDC": "0003-3774",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Opdivo",
      "NonProprietaryName": "Nivolumab",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20141222",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125554",
      "LabelerName": "E.R. Squibb & Sons, L.L.C.",
      "SubstanceName": "NIVOLUMAB",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-08-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20141222",
      "SamplePackage": "N",
      "IndicationAndUsage": "OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).",
      "Description": "Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6."
    },
    {
      "NDCCode": "0003-7125-11",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (0003-7125-11)  / 20 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00003-7125-11",
      "ProductNDC": "0003-7125",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Opdualag",
      "NonProprietaryName": "Nivolumab And Relatlimab-rmbw",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20220318",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA761234",
      "LabelerName": "E.R. Squibb & Sons, L.L.C.",
      "SubstanceName": "NIVOLUMAB; RELATLIMAB",
      "StrengthNumber": "12; 4",
      "StrengthUnit": "mg/mL; mg/mL",
      "Pharm_Classes": "Lymphocyte Activation Gene-3 Antagonists [MoA], Lymphocyte Activation Gene-3 Blocker [EPC], Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-06-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20220318",
      "SamplePackage": "N",
      "IndicationAndUsage": "OPDUALAG is indicated for the treatment of adult and pediatric patients 12 years of age or older with unresectable or metastatic melanoma.",
      "Description": "Nivolumab and relatlimab-rmbw is a fixed-dose combination of two IgG4 kappa monoclonal antibodies (mAbs). Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody that has a calculated molecular mass of 146 kDa and is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. Relatlimab is a lymphocyte activation gene-3 (LAG-3) blocking antibody that has a calculated molecular mass of 148 kDa and is expressed in a recombinant CHO cell line. OPDUALAG (nivolumab and relatlimab-rmbw) injection is a sterile, preservative-free, clear to opalescent, colorless to slightly yellow solution that may contain few translucent-to-white particles. OPDUALAG is supplied as 240 mg of nivolumab and 80 mg of relatlimab in a 20 mL single-dose vial for intravenous use. Each mL of OPDUALAG solution contains 12 mg of nivolumab, 4 mg of relatlimab, and histidine (1.1 mg), L-histidine hydrochloride monohydrate (2.7 mg), pentetic acid (0.008 mg), polysorbate 80 (0.5 mg), sucrose (85.6 mg), and Water for Injection, USP. The pH is 5.8."
    },
    {
      "NDCCode": "0404-9768-30",
      "PackageDescription": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9768-30)  / 30 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "00404-9768-30",
      "ProductNDC": "0404-9768",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Marcaine",
      "NonProprietaryName": "Bupivacine Hydrochloride",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "EPIDURAL; INTRACAUDAL; PERINEURAL",
      "StartMarketingDate": "20260126",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA016964",
      "LabelerName": "Henry Schein, Inc.",
      "SubstanceName": "BUPIVACAINE HYDROCHLORIDE",
      "StrengthNumber": "5",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]",
      "Status": "Active",
      "LastUpdate": "2026-02-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260126",
      "SamplePackage": "N",
      "IndicationAndUsage": "MARCAINE / MARCAINE WITH EPINEPHRINE is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Specific concentrations and presentations of MARCAINE / MARCAINE WITH EPINEPHRINE are recommended for each type of block indicated to produce local or regional anesthesia or analgesia [see Dosage and Administration (2.2)]. Limitations of Use. Not all blocks are indicated for use with MARCAINE / MARCAINE WITH EPINEPHRINE given clinically significant risks associated with use [see Dosage and Administration (2.2), Contraindications (4), Warnings and Precautions (5.1, 5.4, 5.5, 5.7, 5.9)].",
      "Description": "MARCAINE / MARCAINE WITH EPINEPHRINE contains bupivacaine hydrochloride, an amide local anesthetic, as the active pharmaceutical ingredient. The route of administration for MARCAINE (without epinephrine) is by injection, for infiltration, perineural, caudal, epidural, or retrobulbar use. The route of administration for MARCAINE WITH EPINEPHRINE is by injection, for infiltration, perineural, caudal, or epidural use. Multiple-dose vials contain methylparaben [see Warnings and Precautions (5.4)]. Bupivacaine hydrochloride is 2-piperidinecarboxamide, 1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride, monohydrate. It is a white crystalline powder that is freely soluble in 95 percent ethanol, soluble in water, and slightly soluble in chloroform or acetone. It has the following structural formula. MARCAINE with 1:200,000 epinephrine, contains bupivacaine hydrochloride and epinephrine bitartrate (an alpha and beta-adrenergic agonist) as active pharmaceutical ingredients. This product is for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Multiple dose vials contain methylparaben and they should not be used for caudal and lumbar epidural blocks. Epinephrine bitartrate is (–) - 3,4-Dihydroxy-α-[(methylamino)methyl] benzyl alcohol (+)-tartrate (1:1) salt. Epinephrine is a vasoconstrictor. It has the following structural formula. MARCAINE (bupivacaine hydrochloride) is a clear and colorless sterile isotonic solution. Each mL of single-dose vial contains 2.5 mg, 5 mg or 7.5 mg of bupivacaine hydrochloride (equivalent to 2.22 mg, 4.44 mg or 6.66 mg of bupivacaine, respectively), sodium chloride for isotonicity, sodium hydroxide or hydrochloric acid to adjust the pH between 4 and 6.5, in water for injection. For the Multiple-dose vials, each mL also contains 1 mg methylparaben as preservative. MARCAINE with epinephrine 1:200,000 (as bitartrate) is a clear and colorless sterile isotonic solution. Each mL contains 2.5 mg or 5 mg bupivacaine hydrochloride (equivalent to 2.22 mg or 4.44 mg of bupivacaine, respectively), and 0.0091 mg epinephrine bitartrate (equivalent to 0.005 mg of epinephrine), with sodium chloride for isotonicity, 0.5 mg sodium metabisulfite, 0.001 mL monothioglycerol, and 2 mg ascorbic acid as antioxidants, 0.0017 mL 60% sodium lactate buffer, and 0.1 mg edetate calcium disodium as stabilizer. The pH of these solutions is adjusted to between 3.4 and 4.5 with sodium hydroxide or hydrochloric acid. For the Multiple-dose vials, each mL also contains 1 mg methylparaben as preservative. The specific gravity of MARCAINE 0.5% with epinephrine 1:200,000 (as bitartrate) at 25°C is 1.008 and at 37°C is 1.008."
    }
  ]
}
                    

{"NDC":[{"NDCCode":"27281-008-96","ProprietaryName":"Heartery","NonProprietaryName":"American Ginseng, Arnica Montana, Gold, Barium Carbonate, Atropa Belladonna, Calcium Fluoride, Cholesterol, Herring Sperm Dna, Ginkgo, Saccharomyces Cerevisia Rna, Visbum Album Fruiting Top, And Ginger"},{"NDCCode":"27281-001-96","ProprietaryName":"Brain Power","NonProprietaryName":"Semecarpus Anacardium Juice, Arnica Montana, Calcium Fluoride, Silybum Marianum Seed, Chincona Officinalis Bark, Herring Sperm Dna, Ginkgo, Egg Phospholipids, Achillea Millefolium, Phosphoric Acid, Saccharomyces Cerevisia Rna, Silicon Dioxide, And Zinc Sulphate Heptahydrate"},{"NDCCode":"27281-002-96","ProprietaryName":"Livergen","NonProprietaryName":"Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale"},{"NDCCode":"27281-004-96","ProprietaryName":"Immune Booster","NonProprietaryName":"Apis Mellifera, Baptisia Tinctoria, Silybum Marianum Seed, Herring Sperm Dna, Echinacea, Galium Aparine, Mercuric Chloride, Mercuric Sulfide, Nitric Acid, Sulfur Iodide, And Thuja Occidentalis Leafy Twig"},{"NDCCode":"27281-007-96","ProprietaryName":"Diabetigen","NonProprietaryName":"Arnica Montana, Arsenic Trioxide, Herring Sperm Nda, Echinacea, Unspecified, Hamamelis Virginiana Leaf, Chamaelirium Luteum Root, Pork Liver, Iris Versicolor Root, Sus Scrofa Pancreas, Phosphoric Acid, Rosmarinus Officinalis Flowering Top, Claviceps Purpurea Sclerotium, Syzygium Cumini Seed, And Uranyl Nitrate Hexahydrate"},{"NDCCode":"27281-009-96","ProprietaryName":"Female Energy","NonProprietaryName":"Chaste Tree, Arnica Montana, Caulophyllum Thalictroides Root, Cinchona Officinalis Bark, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Lactuca Virosa, Onosmodium Virginianum Whole, Sus Scrofa Ovary, Phosphoric Acid, Sus Scrofa Pituitary Gland, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig"},{"NDCCode":"27281-010-96","ProprietaryName":"Male Tonicity","NonProprietaryName":"American Ginseng, Arnica Montana, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Galium Aparine, Hamamelis Virginiana Root Bark/stem Bark, Pork Liver, Cervus Elaphus Horn Oil, Ovis Aries Testicle, Phosphoric Acid, Sus Scrofa Pituitary Gland, Thuja Occidentalis Leafy Twig, Thyroid, Unspecified, Tribulus Terrestris, Ginger"},{"NDCCode":"27281-011-96","ProprietaryName":"Lung Detox","NonProprietaryName":"Silver Nitrate, Arsenic Trioxide, Activated Charcoal, Silybum Marianum Seed, Herring Sperm Dna, Pork Liver, Mercuric Chloride, Lead"},{"NDCCode":"54273-008-01","ProprietaryName":"Zims Max Freeze","NonProprietaryName":"Menthol"},{"NDCCode":"54641-008-01","ProprietaryName":"Flex24 Pain","NonProprietaryName":"Camphor Menthol"},{"NDCCode":"71481-008-01","ProprietaryName":"Bio V Antacid Berry 96ct","NonProprietaryName":"Calcium Carbonate"},{"NDCCode":"72351-008-00","ProprietaryName":"Rite Aid Roll-on","NonProprietaryName":"Menthol"},{"NDCCode":"72476-008-96","ProprietaryName":"Hand Wash","NonProprietaryName":"Benzalkonium Chloride"},{"NDCCode":"10631-008-30","ProprietaryName":"Kapspargo","NonProprietaryName":"Metoprolol Succinate"},{"NDCCode":"49967-008-01","ProprietaryName":"La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Broad Spectrum Spf 60 Water Resistant 80 Minutes","NonProprietaryName":"Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone"},{"NDCCode":"52720-008-01","ProprietaryName":"Ariel Premium Supply Hand Sanitizer","NonProprietaryName":"Hand Sanitizer"},{"NDCCode":"63304-008-30","ProprietaryName":"Metoprolol Succinate","NonProprietaryName":"Metoprolol Succinate"},{"NDCCode":"73159-008-60","ProprietaryName":"Ultravate","NonProprietaryName":"Halobetasol Propionate"},{"NDCCode":"85437-008-60","ProprietaryName":"Halobetasol Propionate","NonProprietaryName":"Halobetasol Propionate"},{"NDCCode":"27281-003-01","ProprietaryName":"Vivacity","NonProprietaryName":"Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water"},{"NDCCode":"27281-003-02","ProprietaryName":"Vivacity","NonProprietaryName":"Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water"},{"NDCCode":"27281-029-63","ProprietaryName":"Livergen","NonProprietaryName":"Arnica Montana, Bryonia, Carduus Marianus, Chelidonium Majus, Dna, Hepar Suis, Oleum Animale, Pancreas Suis, Taraxacum Officinale."},{"NDCCode":"27281-039-64","ProprietaryName":"Vivacity","NonProprietaryName":"Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, Rna, Thuja Occidentalis"},{"NDCCode":"27281-049-65","ProprietaryName":"Immune Booster","NonProprietaryName":"Apis Mellifica, Baptisia Tinctoria, Carduus Marianus, Echinacea Angustifolia, Gallum Aparine, Mercurius Corrosivus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Sulphur Iodatum, Thuja Occidentalis."},{"NDCCode":"0003-3734-13","ProprietaryName":"Opdivo","NonProprietaryName":"Nivolumab"},{"NDCCode":"0003-3756-14","ProprietaryName":"Opdivo","NonProprietaryName":"Nivolumab"},{"NDCCode":"0003-3772-11","ProprietaryName":"Opdivo","NonProprietaryName":"Nivolumab"},{"NDCCode":"0003-3774-12","ProprietaryName":"Opdivo","NonProprietaryName":"Nivolumab"},{"NDCCode":"0003-7125-11","ProprietaryName":"Opdualag","NonProprietaryName":"Nivolumab And Relatlimab-rmbw"},{"NDCCode":"0404-9768-30","ProprietaryName":"Marcaine","NonProprietaryName":"Bupivacine Hydrochloride"}]}
                    

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<NDCList>
  <NDC>
    <NDCCode>27281-008-96</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-008-96)</PackageDescription>
    <NDC11Code>27281-0008-96</NDC11Code>
    <ProductNDC>27281-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Heartery</ProprietaryName>
    <NonProprietaryName>American Ginseng, Arnica Montana, Gold, Barium Carbonate, Atropa Belladonna, Calcium Fluoride, Cholesterol, Herring Sperm Dna, Ginkgo, Saccharomyces Cerevisia Rna, Visbum Album Fruiting Top, And Ginger</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131209</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>AMERICAN GINSENG; ARNICA MONTANA; GOLD; BARIUM CARBONATE; ATROPA BELLADONNA; CALCIUM FLUORIDE; CHOLESTEROL; HERRING SPERM DNA; GINKGO; SACCHAROMYCES CEREVISIAE RNA; VISCUM ALBUM FRUITING TOP; GINGER</SubstanceName>
    <StrengthNumber>1; 1.5; 30; 30; 3; 6; 15; 3; 3; 3; 1.5; 30</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves symptoms associated with hypertension, such as: high blood pressure; constricted blood vessels; arteriosclerosis; inelastic blood vessels.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-001-96</NDCCode>
    <PackageDescription>30 mL in 1 PACKAGE (27281-001-96)</PackageDescription>
    <NDC11Code>27281-0001-96</NDC11Code>
    <ProductNDC>27281-001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Brain Power</ProprietaryName>
    <NonProprietaryName>Semecarpus Anacardium Juice, Arnica Montana, Calcium Fluoride, Silybum Marianum Seed, Chincona Officinalis Bark, Herring Sperm Dna, Ginkgo, Egg Phospholipids, Achillea Millefolium, Phosphoric Acid, Saccharomyces Cerevisia Rna, Silicon Dioxide, And Zinc Sulphate Heptahydrate</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131118</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>SEMECARPUS ANACARDIUM JUICE; ARNICA MONTANA; CALCIUM FLUORIDE; SILYBUM MARIANUM SEED OIL; CINCHONA OFFICINALIS BARK; HERRING SPERM DNA; GINKGO; EGG PHOSPHOLIPIDS; ACHILLEA MILLEFOLIUM; PHOSPHORIC ACID; SACCHAROMYCES CEREVISIAE RNA; SILICON DIOXIDE; ZINC SULFATE HEPTAHYDRATE</SubstanceName>
    <StrengthNumber>30; 1.5; 30; 1.5; 3; 3; 3; 6; 1.5; 30; 6; 6; 6</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves symptoms of mental fatigue, including: lapses in memory; feelings of confusion or difficulty collecting one's thoughts; short attention span; poor mood.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-002-96</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-002-96)</PackageDescription>
    <NDC11Code>27281-0002-96</NDC11Code>
    <ProductNDC>27281-002</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Livergen</ProprietaryName>
    <NonProprietaryName>Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ARNICA MONTANA; BRYONIA ALBA ROOT; SILYBUM MARIANUM SEED OIL; CHELIDONIUM MAJUS; HERRING SPERM DNA; PORK LIVER; CERVUS ELAPHUS HORN OIL; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE</SubstanceName>
    <StrengthNumber>1.5; 200; .5; 200; 3; 3; 4; 4; 1</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Helps detoxify the liver and temporarily relieves symptoms associated with an overworked or toxic liver, including: fatigue; poor sugar metabolism; poor liver function; ill effects of excessive alcohol consumption.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-004-96</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-004-96)</PackageDescription>
    <NDC11Code>27281-0004-96</NDC11Code>
    <ProductNDC>27281-004</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Immune Booster</ProprietaryName>
    <NonProprietaryName>Apis Mellifera, Baptisia Tinctoria, Silybum Marianum Seed, Herring Sperm Dna, Echinacea, Galium Aparine, Mercuric Chloride, Mercuric Sulfide, Nitric Acid, Sulfur Iodide, And Thuja Occidentalis Leafy Twig</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>APIS MELLIFERA; BAPTISIA TINCTORIA; SILYBUM MARIANUM SEED OIL; HERRING SPERM DNA; ECHINACEA, UNSPECIFIED; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>200; 3; 1.5; 3; 3; 1.5; 200; 30; 30; 200; 200</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Helps support the body's natural defense mechanisms and temporarily relieves: tendencies toward flu &amp; cold; joint pain; minor allergies; low endocrine function.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-007-96</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-007-96)</PackageDescription>
    <NDC11Code>27281-0007-96</NDC11Code>
    <ProductNDC>27281-007</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Diabetigen</ProprietaryName>
    <NonProprietaryName>Arnica Montana, Arsenic Trioxide, Herring Sperm Nda, Echinacea, Unspecified, Hamamelis Virginiana Leaf, Chamaelirium Luteum Root, Pork Liver, Iris Versicolor Root, Sus Scrofa Pancreas, Phosphoric Acid, Rosmarinus Officinalis Flowering Top, Claviceps Purpurea Sclerotium, Syzygium Cumini Seed, And Uranyl Nitrate Hexahydrate</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131209</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ARNICA MONTANA; ARSENIC TRIOXIDE; HERRING SPERM DNA; ECHINACEA, UNSPECIFIED; HAMAMELIS VIRGINIANA LEAF; CHAMAELIRIUM LUTEUM ROOT; PORK LIVER; IRIS VERSICOLOR ROOT; SUS SCROFA PANCREAS; PHOSPHORIC ACID; ROSMARINUS OFFICINALIS FLOWERING TOP; CLAVICEPS PURPUREA SCLEROTIUM; SYZYGIUM CUMINI SEED; URANYL NITRATE HEXAHYDRATE</SubstanceName>
    <StrengthNumber>1.5; 200; 3; 1.5; 1.5; 1.5; 3; 3; 3; 200; 1.5; 30; 1.5; 30</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications:  Temporarily relieves symptoms associated with type II diabetes, including: pancreatic deficiency; liver weakness; apathy and generalized feelings of weakness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-009-96</NDCCode>
    <PackageDescription>30 mg in 1 BOTTLE, SPRAY (27281-009-96)</PackageDescription>
    <NDC11Code>27281-0009-96</NDC11Code>
    <ProductNDC>27281-009</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Female Energy</ProprietaryName>
    <NonProprietaryName>Chaste Tree, Arnica Montana, Caulophyllum Thalictroides Root, Cinchona Officinalis Bark, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Lactuca Virosa, Onosmodium Virginianum Whole, Sus Scrofa Ovary, Phosphoric Acid, Sus Scrofa Pituitary Gland, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140807</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>CHASTE TREE; ARNICA MONTANA; CAULOPHYLLUM THALICTROIDES ROOT; CINCHONA OFFICINALIS BARK; TURNERA DIFFUSA LEAFY TWIG; HERRING SPERM DNA; LACTUCA VIROSA; ONOSMODIUM VIRGINIANUM WHOLE; SUS SCROFA OVARY; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>1.5; 1.5; 3; 1.5; .5; 3; 1.5; 30; 30; 200; 6; 30; 30</StrengthNumber>
    <StrengthUnit>[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves some symptoms of low female sexual energy, such as: decrease in sexual desire; feelings of fatigue; decrease in responsiveness and enjoyment.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-010-96</NDCCode>
    <PackageDescription>30 mg in 1 BOTTLE, SPRAY (27281-010-96)</PackageDescription>
    <NDC11Code>27281-0010-96</NDC11Code>
    <ProductNDC>27281-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Male Tonicity</ProprietaryName>
    <NonProprietaryName>American Ginseng, Arnica Montana, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Galium Aparine, Hamamelis Virginiana Root Bark/stem Bark, Pork Liver, Cervus Elaphus Horn Oil, Ovis Aries Testicle, Phosphoric Acid, Sus Scrofa Pituitary Gland, Thuja Occidentalis Leafy Twig, Thyroid, Unspecified, Tribulus Terrestris, Ginger</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140808</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>AMERICAN GINSENG; ARNICA MONTANA; TURNERA DIFFUSA LEAFY TWIG; HERRING SPERM DNA; GALIUM APARINE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; PORK LIVER; CERVUS ELAPHUS HORN OIL; OVIS ARIES TESTICLE; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; THUJA OCCIDENTALIS LEAFY TWIG; THYROID, UNSPECIFIED; TRIBULUS TERRESTRIS; GINGER</SubstanceName>
    <StrengthNumber>1.5; 1.5; 1; 3; 1.5; 1.5; 3; 4; 3; 200; 4; 1.5; 6; 1; 1.5</StrengthNumber>
    <StrengthUnit>[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves symptoms of low male sexual energy, including: decrease in sexual desire; feelings of fatigue; decrease in performance and enjoyment.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-011-96</NDCCode>
    <PackageDescription>30 mg in 1 BOTTLE, SPRAY (27281-011-96)</PackageDescription>
    <NDC11Code>27281-0011-96</NDC11Code>
    <ProductNDC>27281-011</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Lung Detox</ProprietaryName>
    <NonProprietaryName>Silver Nitrate, Arsenic Trioxide, Activated Charcoal, Silybum Marianum Seed, Herring Sperm Dna, Pork Liver, Mercuric Chloride, Lead</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140808</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>SILVER NITRATE; ARSENIC TRIOXIDE; ACTIVATED CHARCOAL; SILYBUM MARIANUM SEED; HERRING SPERM DNA; PORK LIVER; MERCURIC CHLORIDE; LEAD</SubstanceName>
    <StrengthNumber>200; 200; 200; .5; 3; 3; 200; 200</StrengthNumber>
    <StrengthUnit>[hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Detoxifies the lungs and provides temporary relief from symtpoms associated with inhaling polluted air, both indoors and outdoors, such as: shortness of breath; wheezing; coughing; lack of energy.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>54273-008-01</NDCCode>
    <PackageDescription>96 g in 1 CAN (54273-008-01) </PackageDescription>
    <NDC11Code>54273-0008-01</NDC11Code>
    <ProductNDC>54273-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Zims Max Freeze</ProprietaryName>
    <ProprietaryNameSuffix>Pro Formula</ProprietaryNameSuffix>
    <NonProprietaryName>Menthol</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20180924</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M017</ApplicationNumber>
    <LabelerName>KOBAYASHI Healthcare International, Inc.</LabelerName>
    <SubstanceName>MENTHOL, UNSPECIFIED FORM</SubstanceName>
    <StrengthNumber>160</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-11-18</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180924</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor aches and pains of muscles and joints associated with: 1 Simple backache, 2 Arthritis, 3 Strains, 4 Bruises, 5 Sprains.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>54641-008-01</NDCCode>
    <PackageDescription>96 g in 1 CONTAINER (54641-008-01) </PackageDescription>
    <NDC11Code>54641-0008-01</NDC11Code>
    <ProductNDC>54641-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Flex24 Pain</ProprietaryName>
    <NonProprietaryName>Camphor Menthol</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20190222</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>Larasan Pharmaceutical Corporation</LabelerName>
    <SubstanceName>CAMPHOR (NATURAL); MENTHOL</SubstanceName>
    <StrengthNumber>3; 10</StrengthNumber>
    <StrengthUnit>1/100g; g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190222</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For temporary relief of minor aches and pains of muscle and joints associated with simple backache, arthritis, strains, cramps, bruises, and sprains.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>71481-008-01</NDCCode>
    <PackageDescription>96 TABLET in 1 BOTTLE (71481-008-01) </PackageDescription>
    <NDC11Code>71481-0008-01</NDC11Code>
    <ProductNDC>71481-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bio V Antacid Berry 96ct</ProprietaryName>
    <NonProprietaryName>Calcium Carbonate</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20220228</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M001</ApplicationNumber>
    <LabelerName>BioV Health Inc</LabelerName>
    <SubstanceName>CALCIUM CARBONATE</SubstanceName>
    <StrengthNumber>750</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2025-07-30</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220228</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Relieves  acid indigestion  heartburn  sour stomach  upset stomach associated with these symptoms.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>72351-008-00</NDCCode>
    <PackageDescription>96 GEL in 1 PACKAGE (72351-008-00) </PackageDescription>
    <NDC11Code>72351-0008-00</NDC11Code>
    <ProductNDC>72351-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Rite Aid Roll-on</ProprietaryName>
    <NonProprietaryName>Menthol</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20180809</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>SOTAC PHARMACEUTICALS PRIVATE LIMITED</LabelerName>
    <SubstanceName>MENTHOL</SubstanceName>
    <StrengthNumber>40</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180809</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporary relief from minor aches and pains of sore muscles and joints associated with:  - arthritis, - backache,  - strains, - sprains.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>72476-008-96</NDCCode>
    <PackageDescription>221 mL in 1 BOTTLE, PUMP (72476-008-96) </PackageDescription>
    <NDC11Code>72476-0008-96</NDC11Code>
    <ProductNDC>72476-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Hand Wash</ProprietaryName>
    <NonProprietaryName>Benzalkonium Chloride</NonProprietaryName>
    <DosageFormName>SOAP</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20141002</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part333A</ApplicationNumber>
    <LabelerName>RETAIL BUSINESS SERVICES , LLC</LabelerName>
    <SubstanceName>BENZALKONIUM CHLORIDE</SubstanceName>
    <StrengthNumber>1.3</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2023-09-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20231231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20141002</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>10631-008-30</NDCCode>
    <PackageDescription>30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-008-30) </PackageDescription>
    <NDC11Code>10631-0008-30</NDC11Code>
    <ProductNDC>10631-008</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Kapspargo</ProprietaryName>
    <NonProprietaryName>Metoprolol Succinate</NonProprietaryName>
    <DosageFormName>CAPSULE, EXTENDED RELEASE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20180315</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA210428</ApplicationNumber>
    <LabelerName>Sun Pharmaceutical Industries, Inc.</LabelerName>
    <SubstanceName>METOPROLOL SUCCINATE</SubstanceName>
    <StrengthNumber>25</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2023-04-20</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180315</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>KAPSPARGO Sprinkle is a beta1-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) Angina Pectoris. (1.2) Heart Failure, to reduce the risk of cardiovascular mortality and heart-failure hospitalizations in patients with heart failure. (1.3).</IndicationAndUsage>
    <Description>Metoprolol succinate, is a beta1-selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release capsules. Metoprolol succinate extended-release capsules have been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The extended-release capsules comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets. Each pellet acts as a separate drug delivery unit and is designed to deliver metoprolol continuously over the dosage interval. The extended-release capsules contain 10.24 mg, 20.48 mg, 40.96 mg, and 81.92 mg of metoprolol free base, present as 23.75 mg, 47.5 mg, 95 mg, and 190 mg of metoprolol succinate and are equivalent to 25 mg, 50 mg, 100 mg, and 200 mg of metoprolol tartrate, USP, respectively. Its chemical name is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)phenoxy]-2-propanol succinate (2:1) (salt). Its structural formula is. Metoprolol succinate, USP is a white to off-white powder with a molecular weight of 652.82. It is freely soluble in water, soluble in methanol, sparingly soluble in alcohol, slightly soluble in isopropyl alcohol. Inactive ingredients: ethyl cellulose, hypromellose, polyethylene glycol 400, polyethylene glycol 6000, sugar spheres (corn starch and sucrose), talc and triethyl citrate. The capsule shell and imprinting ink has the following composition: ferric oxide yellow (25 mg, 50 mg and 200 mg), ferrosoferric oxide, gelatin, potassium hydroxide, propylene glycol, shellac and titanium dioxide.</Description>
  </NDC>
  <NDC>
    <NDCCode>49967-008-01</NDCCode>
    <PackageDescription>143 g in 1 BOTTLE, SPRAY (49967-008-01) </PackageDescription>
    <NDC11Code>49967-0008-01</NDC11Code>
    <ProductNDC>49967-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Broad Spectrum Spf 60 Water Resistant 80 Minutes</ProprietaryName>
    <NonProprietaryName>Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20140101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M020</ApplicationNumber>
    <LabelerName>L'Oreal USA Products Inc</LabelerName>
    <SubstanceName>AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE</SubstanceName>
    <StrengthNumber>26.8; 96; 28.8; 53.8; 34.6</StrengthNumber>
    <StrengthUnit>mg/g; mg/g; mg/g; mg/g; mg/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-01-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20140101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>52720-008-01</NDCCode>
    <PackageDescription>8 mL in 1 VIAL (52720-008-01) </PackageDescription>
    <NDC11Code>52720-0008-01</NDC11Code>
    <ProductNDC>52720-008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Ariel Premium Supply Hand Sanitizer</ProprietaryName>
    <NonProprietaryName>Hand Sanitizer</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20200820</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part333E</ApplicationNumber>
    <LabelerName>ZHONGSHAN S. JANE BIOTECHNOLOGY CO., LTD.</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>4.96</StrengthNumber>
    <StrengthUnit>mL/8mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-02-19</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20200820</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>63304-008-30</NDCCode>
    <PackageDescription>30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-008-30) </PackageDescription>
    <NDC11Code>63304-0008-30</NDC11Code>
    <ProductNDC>63304-008</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Metoprolol Succinate</ProprietaryName>
    <NonProprietaryName>Metoprolol Succinate</NonProprietaryName>
    <DosageFormName>CAPSULE, EXTENDED RELEASE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20180207</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA210428</ApplicationNumber>
    <LabelerName>Sun Pharmaceutical Industries Inc.</LabelerName>
    <SubstanceName>METOPROLOL SUCCINATE</SubstanceName>
    <StrengthNumber>25</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2018-02-09</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180207</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Metoprolol succinate extended-release capsules are beta1-selective adrenoceptor blocking agent indicated for the treatment of: : 1 Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) , 2 Angina Pectoris. (1.2) , 3 Heart Failure, to reduce the risk of cardiovascular mortality and heart-failure hospitalization in patients with heart failure. (1.3).</IndicationAndUsage>
    <Description>Metoprolol succinate, is a beta1-selective (cardioselective) adrenoceptor blocking agent, for oral administration, available as extended-release capsules. Metoprolol succinate extended-release capsules have been formulated to provide a controlled and predictable release of metoprolol for once-daily administration. The extended-release capsules comprise a multiple unit system containing metoprolol succinate in a multitude of controlled release pellets. Each pellet acts as a separate drug delivery unit and is designed to deliver metoprolol continuously over the dosage interval. The extended-release capsules contain 10.24 mg, 20.48 mg, 40.96 mg, and 81.92 mg of metoprolol free base, present as 23.75 mg, 47.5 mg, 95 mg, and 190 mg of metoprolol succinate and are equivalent to 25 mg, 50 mg, 100 mg, and 200 mg of metoprolol tartrate, USP, respectively. Its chemical name is (±)-1-(Isopropylamino)-3-[p-(2-methoxyethyl)phenoxy]-2-propanol succinate (2:1) (salt). Its structural formula is. Metoprolol succinate, USP is a white to off-white powder with a molecular weight of 652.82. It is freely soluble in water, soluble in methanol, sparingly soluble in alcohol, slightly soluble in isopropyl alcohol. Inactive ingredients: ethyl cellulose, hypromellose, polyethylene glycol 400, polyethylene glycol 6000, sugar spheres (corn starch and sucrose), talc and triethyl citrate. The capsule shell and imprinting ink has the following composition: ferric oxide yellow (25 mg, 50 mg and 200 mg), ferrosoferric oxide, gelatin, potassium hydroxide, propylene glycol, shellac and titanium dioxide.</Description>
  </NDC>
  <NDC>
    <NDCCode>73159-008-60</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (73159-008-60)  / 59 g in 1 BOTTLE</PackageDescription>
    <NDC11Code>73159-0008-60</NDC11Code>
    <ProductNDC>73159-008</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Ultravate</ProprietaryName>
    <NonProprietaryName>Halobetasol Propionate</NonProprietaryName>
    <DosageFormName>LOTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20250406</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA208183</ApplicationNumber>
    <LabelerName>Lacer Pharma, LLC</LabelerName>
    <SubstanceName>HALOBETASOL PROPIONATE</SubstanceName>
    <StrengthNumber>.5</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Pharm_Classes>Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-05-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250406</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>ULTRAVATE lotion is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.</IndicationAndUsage>
    <Description>ULTRAVATE (halobetasol propionate) lotion, 0.05% for topical use contains a corticosteroid, halobetasol propionate. The chemical name of halobetasol propionate is 21­ chloro-6α, 9-difluoro-11β, 17-dihydroxy-16β-methylpregna-1, 4-diene-3,20-dione 17­ propionate. Halobetasol propionate is a white to off-white crystalline powder with a molecular weight of 484.96 and a molecular formula of C 25H 31ClF 2O 5. It is practically insoluble in water and freely soluble in dichloromethane and in acetone. It has the following structural formula:. Each gram of ULTRAVATE lotion contains 0.5 mg of halobetasol propionate in a white to off-white lotion base consisting of diisopropyl adipate, octyldodecanol, ceteth-20, poloxamer 407, cetyl alcohol, stearyl alcohol, propylparaben, butylparaben, propylene glycol, glycerin, carbomer homopolymer, sodium hydroxide, and water.</Description>
  </NDC>
  <NDC>
    <NDCCode>85437-008-60</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (85437-008-60)  / 59 g in 1 BOTTLE</PackageDescription>
    <NDC11Code>85437-0008-60</NDC11Code>
    <ProductNDC>85437-008</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Halobetasol Propionate</ProprietaryName>
    <NonProprietaryName>Halobetasol Propionate</NonProprietaryName>
    <DosageFormName>LOTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20260310</StartMarketingDate>
    <EndMarketingDate>20270531</EndMarketingDate>
    <MarketingCategoryName>NDA AUTHORIZED GENERIC</MarketingCategoryName>
    <ApplicationNumber>NDA208183</ApplicationNumber>
    <LabelerName>Coral Way Pharma, LLC</LabelerName>
    <SubstanceName>HALOBETASOL PROPIONATE</SubstanceName>
    <StrengthNumber>.5</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Pharm_Classes>Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-07-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20260310</StartMarketingDatePackage>
    <EndMarketingDatePackage>20270531</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Halobetasol Propionate Lotion 0.05% is indicated for the topical treatment of plaque psoriasis in patients 12 years of age and older.</IndicationAndUsage>
    <Description>Halobetasol Propionate Lotion 0.05% for topical use contains a corticosteroid, halobetasol propionate. The chemical name of halobetasol propionate is 21­ chloro-6α, 9-difluoro-11β, 17-dihydroxy-16β-methylpregna-1, 4-diene-3,20-dione 17­ propionate. Halobetasol propionate is a white to off-white crystalline powder with a molecular weight of 484.96 and a molecular formula of C 25H 31ClF 2O 5. It is practically insoluble in water and freely soluble in dichloromethane and in acetone. It has the following structural formula:. Each gram of Halobetasol Propionate Lotion 0.05% contains 0.5 mg of halobetasol propionate in a white to off-white lotion base consisting of diisopropyl adipate, octyldodecanol, ceteth-20, poloxamer 407, cetyl alcohol, stearyl alcohol, propylparaben, butylparaben, propylene glycol, glycerin, carbomer homopolymer, sodium hydroxide, and water.</Description>
  </NDC>
  <NDC>
    <NDCCode>27281-003-01</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-003-01)</PackageDescription>
    <NDC11Code>27281-0003-01</NDC11Code>
    <ProductNDC>27281-003</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Vivacity</ProprietaryName>
    <NonProprietaryName>Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ALFALFA; ARNICA MONTANA; AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; HERRING SPERM DNA; HYPERICUM PERFORATUM; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>1; 1.5; 1; 1; 1.5; 3; 200; 3; 4; 200; 3; 30</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves symptoms of general physical weakness and listlessness, including: fatigue; sore muscles &amp; joints; dry skin; absence of sexual desire; occasional sleeplessness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-003-02</NDCCode>
    <PackageDescription>60 mL in 1 BOTTLE, SPRAY (27281-003-02)</PackageDescription>
    <NDC11Code>27281-0003-02</NDC11Code>
    <ProductNDC>27281-003</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Vivacity</ProprietaryName>
    <NonProprietaryName>Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ALFALFA; ARNICA MONTANA; AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; HERRING SPERM DNA; HYPERICUM PERFORATUM; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>1; 1.5; 1; 1; 1.5; 3; 200; 3; 4; 200; 3; 30</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Indications: Temporarily relieves symptoms of general physical weakness and listlessness, including: fatigue; sore muscles &amp; joints; dry skin; absence of sexual desire; occasional sleeplessness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-029-63</NDCCode>
    <PackageDescription>30 mL in 1 PACKAGE (27281-029-63) </PackageDescription>
    <NDC11Code>27281-0029-63</NDC11Code>
    <ProductNDC>27281-029</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Livergen</ProprietaryName>
    <NonProprietaryName>Arnica Montana, Bryonia, Carduus Marianus, Chelidonium Majus, Dna, Hepar Suis, Oleum Animale, Pancreas Suis, Taraxacum Officinale.</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ARNICA MONTANA; BRYONIA ALBA ROOT; MILK THISTLE; CHELIDONIUM MAJUS; HERRING SPERM DNA; PORK LIVER; CERVUS ELAPHUS HORN OIL; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE</SubstanceName>
    <StrengthNumber>3; 200; 1; 200; 6; 6; 8; 8; 2</StrengthNumber>
    <StrengthUnit>[hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-12-31</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20131113</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​USES: ​Relieves symptoms of aging or a rundown condition, including: Relief for feelings of fatigue that may be caused by an over-worked liver or by liver toxixity; supports proper sugar metabolism; stimulates proper liver function; protects against the ill-effects of excessive alcohol consumption.*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-039-64</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-039-64) </PackageDescription>
    <NDC11Code>27281-0039-64</NDC11Code>
    <ProductNDC>27281-039</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Vivacity</ProprietaryName>
    <NonProprietaryName>Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, Rna, Thuja Occidentalis</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20180205</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>ALFALFA; ARNICA MONTANA; AVENA SATIVA FLOWERING TOP; GALIUM APARINE; PORK LIVER; HYPERICUM PERFORATUM; ASIAN GINSENG; CERVUS ELAPHUS HORN OIL; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; SACCHAROMYCES CEREVISIAE RNA; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>2; 3; 2; 3; 6; 200; 2; 6; 8; 200; 6; 30</StrengthNumber>
    <StrengthUnit>[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-12-31</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180205</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​USES: ​Relieves symptoms of aging or a rundown condition, including: Low energy; poor muscle balance; poor stamina; occssional sleeplessnees.*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>27281-049-65</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, SPRAY (27281-049-65) </PackageDescription>
    <NDC11Code>27281-0049-65</NDC11Code>
    <ProductNDC>27281-049</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Immune Booster</ProprietaryName>
    <NonProprietaryName>Apis Mellifica, Baptisia Tinctoria, Carduus Marianus, Echinacea Angustifolia, Gallum Aparine, Mercurius Corrosivus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Sulphur Iodatum, Thuja Occidentalis.</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131113</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Sunway Biotech LLC</LabelerName>
    <SubstanceName>APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; MILK THISTLE; ECHINACEA ANGUSTIFOLIA; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>200; 6; 3; 6; 3; 200; 30; 30; 200; 200</StrengthNumber>
    <StrengthUnit>[hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-12-31</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20131113</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​USES: ​Supports the body's natural defense mechanisms, temporarily relieves: tendency towards flu &amp; cold; joint pain; minor allergy. Helps balance the body's level of Human Growth Hormone, supporting healthy immune response. Stimulates the endocrine glands*. *Claims based on traditional homeopathic practice, not accepted by medical evidence. Not FDA evaluated.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>0003-3734-13</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3734-13)  / 24 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00003-3734-13</NDC11Code>
    <ProductNDC>0003-3734</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Opdivo</ProprietaryName>
    <NonProprietaryName>Nivolumab</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20171208</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125554</ApplicationNumber>
    <LabelerName>E.R. Squibb &amp; Sons, L.L.C.</LabelerName>
    <SubstanceName>NIVOLUMAB</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-08-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171208</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).</IndicationAndUsage>
    <Description>Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6.</Description>
  </NDC>
  <NDC>
    <NDCCode>0003-3756-14</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3756-14)  / 12 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00003-3756-14</NDC11Code>
    <ProductNDC>0003-3756</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Opdivo</ProprietaryName>
    <NonProprietaryName>Nivolumab</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20210830</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125554</ApplicationNumber>
    <LabelerName>E.R. Squibb &amp; Sons, L.L.C.</LabelerName>
    <SubstanceName>NIVOLUMAB</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-08-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20210830</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).</IndicationAndUsage>
    <Description>Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6.</Description>
  </NDC>
  <NDC>
    <NDCCode>0003-3772-11</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3772-11)  / 4 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00003-3772-11</NDC11Code>
    <ProductNDC>0003-3772</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Opdivo</ProprietaryName>
    <NonProprietaryName>Nivolumab</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20141222</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125554</ApplicationNumber>
    <LabelerName>E.R. Squibb &amp; Sons, L.L.C.</LabelerName>
    <SubstanceName>NIVOLUMAB</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-08-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20141222</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).</IndicationAndUsage>
    <Description>Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6.</Description>
  </NDC>
  <NDC>
    <NDCCode>0003-3774-12</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 CARTON (0003-3774-12)  / 10 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00003-3774-12</NDC11Code>
    <ProductNDC>0003-3774</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Opdivo</ProprietaryName>
    <NonProprietaryName>Nivolumab</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20141222</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125554</ApplicationNumber>
    <LabelerName>E.R. Squibb &amp; Sons, L.L.C.</LabelerName>
    <SubstanceName>NIVOLUMAB</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-08-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20141222</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>OPDIVO is a programmed death receptor-1 (PD-1)-blocking antibody indicated for the treatment of:. Melanoma: 1 adult and pediatric (12 years and older) patients with unresectable or metastatic melanoma, as a single agent or in combination with ipilimumab. (1.1), 2 for the adjuvant treatment of adult and pediatric patients 12 years and older with completely resected Stage IIB, Stage IIC, Stage III, or Stage IV melanoma. (1.2).</IndicationAndUsage>
    <Description>Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody. Nivolumab is an IgG4 kappa immunoglobulin that has a calculated molecular mass of 146 kDa. It is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. OPDIVO is a sterile, preservative-free, non-pyrogenic, clear to opalescent, colorless to pale-yellow liquid that may contain light (few) particles. OPDIVO (nivolumab) injection for intravenous use is supplied in single-dose vials. Each mL of OPDIVO solution contains nivolumab 10 mg, mannitol (30 mg), pentetic acid (0.008 mg), polysorbate 80 (0.2 mg), sodium chloride (2.92 mg), sodium citrate dihydrate (5.88 mg), and Water for Injection, USP. May contain hydrochloric acid and/or sodium hydroxide to adjust pH to 6.</Description>
  </NDC>
  <NDC>
    <NDCCode>0003-7125-11</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 CARTON (0003-7125-11)  / 20 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00003-7125-11</NDC11Code>
    <ProductNDC>0003-7125</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Opdualag</ProprietaryName>
    <NonProprietaryName>Nivolumab And Relatlimab-rmbw</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20220318</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA761234</ApplicationNumber>
    <LabelerName>E.R. Squibb &amp; Sons, L.L.C.</LabelerName>
    <SubstanceName>NIVOLUMAB; RELATLIMAB</SubstanceName>
    <StrengthNumber>12; 4</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL</StrengthUnit>
    <Pharm_Classes>Lymphocyte Activation Gene-3 Antagonists [MoA], Lymphocyte Activation Gene-3 Blocker [EPC], Programmed Death Receptor-1 Blocking Antibody [EPC], Programmed Death Receptor-1-directed Antibody Interactions [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-06-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220318</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>OPDUALAG is indicated for the treatment of adult and pediatric patients 12 years of age or older with unresectable or metastatic melanoma.</IndicationAndUsage>
    <Description>Nivolumab and relatlimab-rmbw is a fixed-dose combination of two IgG4 kappa monoclonal antibodies (mAbs). Nivolumab is a programmed death receptor-1 (PD-1) blocking antibody that has a calculated molecular mass of 146 kDa and is expressed in a recombinant Chinese Hamster Ovary (CHO) cell line. Relatlimab is a lymphocyte activation gene-3 (LAG-3) blocking antibody that has a calculated molecular mass of 148 kDa and is expressed in a recombinant CHO cell line. OPDUALAG (nivolumab and relatlimab-rmbw) injection is a sterile, preservative-free, clear to opalescent, colorless to slightly yellow solution that may contain few translucent-to-white particles. OPDUALAG is supplied as 240 mg of nivolumab and 80 mg of relatlimab in a 20 mL single-dose vial for intravenous use. Each mL of OPDUALAG solution contains 12 mg of nivolumab, 4 mg of relatlimab, and histidine (1.1 mg), L-histidine hydrochloride monohydrate (2.7 mg), pentetic acid (0.008 mg), polysorbate 80 (0.5 mg), sucrose (85.6 mg), and Water for Injection, USP. The pH is 5.8.</Description>
  </NDC>
  <NDC>
    <NDCCode>0404-9768-30</NDCCode>
    <PackageDescription>1 VIAL, SINGLE-DOSE in 1 BAG (0404-9768-30)  / 30 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>00404-9768-30</NDC11Code>
    <ProductNDC>0404-9768</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Marcaine</ProprietaryName>
    <NonProprietaryName>Bupivacine Hydrochloride</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>EPIDURAL; INTRACAUDAL; PERINEURAL</RouteName>
    <StartMarketingDate>20260126</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA016964</ApplicationNumber>
    <LabelerName>Henry Schein, Inc.</LabelerName>
    <SubstanceName>BUPIVACAINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>5</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-02-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260126</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>MARCAINE / MARCAINE WITH EPINEPHRINE is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Specific concentrations and presentations of MARCAINE / MARCAINE WITH EPINEPHRINE are recommended for each type of block indicated to produce local or regional anesthesia or analgesia [see Dosage and Administration (2.2)]. Limitations of Use. Not all blocks are indicated for use with MARCAINE / MARCAINE WITH EPINEPHRINE given clinically significant risks associated with use [see Dosage and Administration (2.2), Contraindications (4), Warnings and Precautions (5.1, 5.4, 5.5, 5.7, 5.9)].</IndicationAndUsage>
    <Description>MARCAINE / MARCAINE WITH EPINEPHRINE contains bupivacaine hydrochloride, an amide local anesthetic, as the active pharmaceutical ingredient. The route of administration for MARCAINE (without epinephrine) is by injection, for infiltration, perineural, caudal, epidural, or retrobulbar use. The route of administration for MARCAINE WITH EPINEPHRINE is by injection, for infiltration, perineural, caudal, or epidural use. Multiple-dose vials contain methylparaben [see Warnings and Precautions (5.4)]. Bupivacaine hydrochloride is 2-piperidinecarboxamide, 1-butyl-N-(2,6-dimethylphenyl)-, monohydrochloride, monohydrate. It is a white crystalline powder that is freely soluble in 95 percent ethanol, soluble in water, and slightly soluble in chloroform or acetone. It has the following structural formula. MARCAINE with 1:200,000 epinephrine, contains bupivacaine hydrochloride and epinephrine bitartrate (an alpha and beta-adrenergic agonist) as active pharmaceutical ingredients. This product is for injection via local infiltration, peripheral nerve block, and caudal and lumbar epidural blocks. Multiple dose vials contain methylparaben and they should not be used for caudal and lumbar epidural blocks. Epinephrine bitartrate is (–) - 3,4-Dihydroxy-α-[(methylamino)methyl] benzyl alcohol (+)-tartrate (1:1) salt. Epinephrine is a vasoconstrictor. It has the following structural formula. MARCAINE (bupivacaine hydrochloride) is a clear and colorless sterile isotonic solution. Each mL of single-dose vial contains 2.5 mg, 5 mg or 7.5 mg of bupivacaine hydrochloride (equivalent to 2.22 mg, 4.44 mg or 6.66 mg of bupivacaine, respectively), sodium chloride for isotonicity, sodium hydroxide or hydrochloric acid to adjust the pH between 4 and 6.5, in water for injection. For the Multiple-dose vials, each mL also contains 1 mg methylparaben as preservative. MARCAINE with epinephrine 1:200,000 (as bitartrate) is a clear and colorless sterile isotonic solution. Each mL contains 2.5 mg or 5 mg bupivacaine hydrochloride (equivalent to 2.22 mg or 4.44 mg of bupivacaine, respectively), and 0.0091 mg epinephrine bitartrate (equivalent to 0.005 mg of epinephrine), with sodium chloride for isotonicity, 0.5 mg sodium metabisulfite, 0.001 mL monothioglycerol, and 2 mg ascorbic acid as antioxidants, 0.0017 mL 60% sodium lactate buffer, and 0.1 mg edetate calcium disodium as stabilizer. The pH of these solutions is adjusted to between 3.4 and 4.5 with sodium hydroxide or hydrochloric acid. For the Multiple-dose vials, each mL also contains 1 mg methylparaben as preservative. The specific gravity of MARCAINE 0.5% with epinephrine 1:200,000 (as bitartrate) at 25°C is 1.008 and at 37°C is 1.008.</Description>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>27281-008-96</NDCCode><ProprietaryName>Heartery</ProprietaryName><NonProprietaryName>American Ginseng, Arnica Montana, Gold, Barium Carbonate, Atropa Belladonna, Calcium Fluoride, Cholesterol, Herring Sperm Dna, Ginkgo, Saccharomyces Cerevisia Rna, Visbum Album Fruiting Top, And Ginger</NonProprietaryName></NDC><NDC><NDCCode>27281-001-96</NDCCode><ProprietaryName>Brain Power</ProprietaryName><NonProprietaryName>Semecarpus Anacardium Juice, Arnica Montana, Calcium Fluoride, Silybum Marianum Seed, Chincona Officinalis Bark, Herring Sperm Dna, Ginkgo, Egg Phospholipids, Achillea Millefolium, Phosphoric Acid, Saccharomyces Cerevisia Rna, Silicon Dioxide, And Zinc Sulphate Heptahydrate</NonProprietaryName></NDC><NDC><NDCCode>27281-002-96</NDCCode><ProprietaryName>Livergen</ProprietaryName><NonProprietaryName>Arnica Montana, Byronia Alba Root, Silybum Marianum Seed, Chelidonium Majus, Herring Sperm Dna, Pork Liver, Cervus Elaphus Horn Oil, Sus Scrofa Pancreas, And Taraxacum Officinale</NonProprietaryName></NDC><NDC><NDCCode>27281-004-96</NDCCode><ProprietaryName>Immune Booster</ProprietaryName><NonProprietaryName>Apis Mellifera, Baptisia Tinctoria, Silybum Marianum Seed, Herring Sperm Dna, Echinacea, Galium Aparine, Mercuric Chloride, Mercuric Sulfide, Nitric Acid, Sulfur Iodide, And Thuja Occidentalis Leafy Twig</NonProprietaryName></NDC><NDC><NDCCode>27281-007-96</NDCCode><ProprietaryName>Diabetigen</ProprietaryName><NonProprietaryName>Arnica Montana, Arsenic Trioxide, Herring Sperm Nda, Echinacea, Unspecified, Hamamelis Virginiana Leaf, Chamaelirium Luteum Root, Pork Liver, Iris Versicolor Root, Sus Scrofa Pancreas, Phosphoric Acid, Rosmarinus Officinalis Flowering Top, Claviceps Purpurea Sclerotium, Syzygium Cumini Seed, And Uranyl Nitrate Hexahydrate</NonProprietaryName></NDC><NDC><NDCCode>27281-009-96</NDCCode><ProprietaryName>Female Energy</ProprietaryName><NonProprietaryName>Chaste Tree, Arnica Montana, Caulophyllum Thalictroides Root, Cinchona Officinalis Bark, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Lactuca Virosa, Onosmodium Virginianum Whole, Sus Scrofa Ovary, Phosphoric Acid, Sus Scrofa Pituitary Gland, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig</NonProprietaryName></NDC><NDC><NDCCode>27281-010-96</NDCCode><ProprietaryName>Male Tonicity</ProprietaryName><NonProprietaryName>American Ginseng, Arnica Montana, Turnera Diffusa Leafy Twig, Herring Sperm Dna, Galium Aparine, Hamamelis Virginiana Root Bark/stem Bark, Pork Liver, Cervus Elaphus Horn Oil, Ovis Aries Testicle, Phosphoric Acid, Sus Scrofa Pituitary Gland, Thuja Occidentalis Leafy Twig, Thyroid, Unspecified, Tribulus Terrestris, Ginger</NonProprietaryName></NDC><NDC><NDCCode>27281-011-96</NDCCode><ProprietaryName>Lung Detox</ProprietaryName><NonProprietaryName>Silver Nitrate, Arsenic Trioxide, Activated Charcoal, Silybum Marianum Seed, Herring Sperm Dna, Pork Liver, Mercuric Chloride, Lead</NonProprietaryName></NDC><NDC><NDCCode>54273-008-01</NDCCode><ProprietaryName>Zims Max Freeze</ProprietaryName><NonProprietaryName>Menthol</NonProprietaryName></NDC><NDC><NDCCode>54641-008-01</NDCCode><ProprietaryName>Flex24 Pain</ProprietaryName><NonProprietaryName>Camphor Menthol</NonProprietaryName></NDC><NDC><NDCCode>71481-008-01</NDCCode><ProprietaryName>Bio V Antacid Berry 96ct</ProprietaryName><NonProprietaryName>Calcium Carbonate</NonProprietaryName></NDC><NDC><NDCCode>72351-008-00</NDCCode><ProprietaryName>Rite Aid Roll-on</ProprietaryName><NonProprietaryName>Menthol</NonProprietaryName></NDC><NDC><NDCCode>72476-008-96</NDCCode><ProprietaryName>Hand Wash</ProprietaryName><NonProprietaryName>Benzalkonium Chloride</NonProprietaryName></NDC><NDC><NDCCode>10631-008-30</NDCCode><ProprietaryName>Kapspargo</ProprietaryName><NonProprietaryName>Metoprolol Succinate</NonProprietaryName></NDC><NDC><NDCCode>49967-008-01</NDCCode><ProprietaryName>La Roche Posay Laboratoire Dermatologique Anthelios 60 Ultra Light Sunscreen Broad Spectrum Spf 60 Water Resistant 80 Minutes</ProprietaryName><NonProprietaryName>Avobenzone, Homosalate, Octisalate, Octocrylene And Oxybenzone</NonProprietaryName></NDC><NDC><NDCCode>52720-008-01</NDCCode><ProprietaryName>Ariel Premium Supply Hand Sanitizer</ProprietaryName><NonProprietaryName>Hand Sanitizer</NonProprietaryName></NDC><NDC><NDCCode>63304-008-30</NDCCode><ProprietaryName>Metoprolol Succinate</ProprietaryName><NonProprietaryName>Metoprolol Succinate</NonProprietaryName></NDC><NDC><NDCCode>73159-008-60</NDCCode><ProprietaryName>Ultravate</ProprietaryName><NonProprietaryName>Halobetasol Propionate</NonProprietaryName></NDC><NDC><NDCCode>85437-008-60</NDCCode><ProprietaryName>Halobetasol Propionate</ProprietaryName><NonProprietaryName>Halobetasol Propionate</NonProprietaryName></NDC><NDC><NDCCode>27281-003-01</NDCCode><ProprietaryName>Vivacity</ProprietaryName><NonProprietaryName>Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water</NonProprietaryName></NDC><NDC><NDCCode>27281-003-02</NDCCode><ProprietaryName>Vivacity</ProprietaryName><NonProprietaryName>Alfalfa, Aralia Quinquefolia, Arnica Montana, Avena Sativa, Dna, Galium Aparine, Hypericum Perforatum, Oleum Animale, Pituitarium Posterium, Rhus Toxicodendron, Rna, Thuja Occidentalis, Alcohol, Glycerin, Water</NonProprietaryName></NDC><NDC><NDCCode>27281-029-63</NDCCode><ProprietaryName>Livergen</ProprietaryName><NonProprietaryName>Arnica Montana, Bryonia, Carduus Marianus, Chelidonium Majus, Dna, Hepar Suis, Oleum Animale, Pancreas Suis, Taraxacum Officinale.</NonProprietaryName></NDC><NDC><NDCCode>27281-039-64</NDCCode><ProprietaryName>Vivacity</ProprietaryName><NonProprietaryName>Alfalfa, Arnica Montana, Avena Sativa, Galium Aparine, Hepar Suis, Hypericum Perforatum, Korean Ginseng, Oleum Animale, Pituitary Suis, Rhus Toxicodendron, Rna, Thuja Occidentalis</NonProprietaryName></NDC><NDC><NDCCode>27281-049-65</NDCCode><ProprietaryName>Immune Booster</ProprietaryName><NonProprietaryName>Apis Mellifica, Baptisia Tinctoria, Carduus Marianus, Echinacea Angustifolia, Gallum Aparine, Mercurius Corrosivus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Sulphur Iodatum, Thuja Occidentalis.</NonProprietaryName></NDC><NDC><NDCCode>0003-3734-13</NDCCode><ProprietaryName>Opdivo</ProprietaryName><NonProprietaryName>Nivolumab</NonProprietaryName></NDC><NDC><NDCCode>0003-3756-14</NDCCode><ProprietaryName>Opdivo</ProprietaryName><NonProprietaryName>Nivolumab</NonProprietaryName></NDC><NDC><NDCCode>0003-3772-11</NDCCode><ProprietaryName>Opdivo</ProprietaryName><NonProprietaryName>Nivolumab</NonProprietaryName></NDC><NDC><NDCCode>0003-3774-12</NDCCode><ProprietaryName>Opdivo</ProprietaryName><NonProprietaryName>Nivolumab</NonProprietaryName></NDC><NDC><NDCCode>0003-7125-11</NDCCode><ProprietaryName>Opdualag</ProprietaryName><NonProprietaryName>Nivolumab And Relatlimab-rmbw</NonProprietaryName></NDC><NDC><NDCCode>0404-9768-30</NDCCode><ProprietaryName>Marcaine</ProprietaryName><NonProprietaryName>Bupivacine Hydrochloride</NonProprietaryName></NDC></NDCList>
                    

Using REST to Invoke DataLabs API

Introduction

This document is intended for developers who want to write applications that can interact with the DataLabs REST API. With DataLabs Web Services, you can create a customized services for your own website or application. You can use the REST API to retrieve DataLabs Web Services results programmatically.

Important: The REST API requires the use of an API key, which you can get from the DataLabs MyAccount Console.

Working With DataLabs REST API

You can retrieve results for a particular operation (search, getcode, etc) by sending an HTTP GET request to its URI.
For instance, the URI for a “search” request has the following format:

https://www.datalabs.health/api/{domain}/{operation}?q={query}&rt={result type}&token={token}

If the request succeeds, the server responds with a 200 OK HTTP status code and the response data.

Four parameters are required with each “search” request:

• Use the domain parameter to specify required data domain.
• Use the operation parameter to specify “format_check” operation.
• Use the q (query) parameter to specify your query.
• Use the token (API key) query parameter to identify your application.

Optional parameter:

• Use the rt (result type) parameter to specify required result type (json/xml/min.json/min.xml).

All other query parameters (if any) are optional.

Full list of API parameters:

• Use the domain parameter to specify required data domain.
• Use the operation parameter to specify “format_check” operation.
• Use the q (query) parameter to specify your query.
• Use the token (API key) query parameter to identify your application.
• Use the tin (tin number) parameter to specify your query about tin number.
• Use the tinname (tin name) parameter to specify your query about tin name.
• Use the zipcode (zip code) parameter to specify your query about zip code.
• Use the radius (radius) parameter to specify your query about radius.
• Use the fromdate (fromdate) parameter to specify your query about from date.
• Use the todate (todate) parameter to specify your query about to date.

Operations Currently Available in the DataLabs REST API

Currently DataLabs RESTful Lookup Service supports following operations:

• check_status — this method allows to get current code status.
• getcode — this method allows retrieval of full infrormation regarding one item based on the provided key.
• getcodes — this method allows retrieval of full infrormation regarding number of items based on the provided keys (q=1285636522,1730198755,1427145176,1487730636).
• search — allows retrieval of set of items based on the free-form lookup query.
• search_and_keywords — returns not only free-form lookup results but also keywords relevant to the original query.

Plus there are three NPI-specific operations:

• validate — allows to determine whether provider's information is valid based on data in the CMS database.
• paginate_with_predicates — provides server side data pagination using sorting and ordering criteria.
• search_with_predicates — this method is a "blend" of free text search and traditional prdeicate-based data selection.
• zipradius — allows to get npis by zipcode & radius.
• npideactivated — allows to get deactivated npis between two dates.

REST Search Examples

Query Parameter Reference

The query parameters you can use with the DataLabs REST API are summarized in the following table.
All parameter values need to be URL encoded.

Use Case #1 - I Need to Find Healthcare Provider (Doctor or Orgranization) Having Just Partial Information

So, you have to find healthcare provider having just partial information. For instance all you have is "EYE doctor RANIA in REDMOND". Strictly speaking, it is necessary to perform a search with minimum information and the maximum level of relevance of the result.

Coding example below demonstrates simplest implementation in C# language. By default DataLabs full text search API returns 30 results and, as you may see below, the first result in the list is "REDMOND EYE DOCTORS, PLLC" where dr. Rania Montecillo specified an owner.

Feel free to use and modify this code to find doctors you may know. If you provide more or less meaningfull information you will be pleasantly surprised to see them in the search results.

            
//--------------------------------------------------------------------------------------
// Fulltext search on NPI registry. Perform "search" operation to get most relevant results.
//--------------------------------------------------------------------------------------
using System;
using System.Net.Http;
using System.Threading.Tasks;

public class Program
{
    private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

    static async Task Main(string[] args)
    {
        string endPoint = $"https://www.datalabs.health/api/npi/search?q=EYE%20RANIA%20REDMOND&token={token}";
        using HttpClient client = new HttpClient();
        string response = await client.GetStringAsync(endPoint);

        Console.WriteLine(response);

        Console.WriteLine("Done. Press any key to exit ...");
        Console.ReadKey();
    }
}
            
        

            
{
  "NPI": [
    {
      "NPI": "1295783033",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "REDMOND EYE DOCTORS, PLLC",
      "FirstLineMailingAddress": "16375 NE 85TH ST",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3554",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-7363",
      "MailingAddressFaxNumber": "425-861-5585",
      "FirstLinePracticeLocationAddress": "16375 NE 85TH ST",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3554",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-7363",
      "PracticeLocationAddressFaxNumber": "425-861-5585",
      "EnumerationDate": "05/04/2006",
      "LastUpdateDate": "12/11/2007",
      "AuthorizedOfficialLastName": "MONTECILLO",
      "AuthorizedOfficialFirstName": "RANIA",
      "AuthorizedOfficialTitle": "OWNER",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "O.D.",
      "AuthorizedOfficialTelephoneNumber": "425-885-7363",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "801TX",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization."
    },
    {
      "NPI": "1346319878",
      "EntityType": "Organization",
      "EIN": "N/A",
      "OrgName": "REDMOND EYE CLINIC PLLC",
      "FirstLineMailingAddress": "16150 NE 85TH ST STE 206",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3543",
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      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

Use Case #2 - I Need to Find Detailed Healthcare Provider Information Using Known NPI Number

This is very common scenario. You need to get full replica of NPI record. Again, it simple. Just use code provided below. API response may contain single NPI record, or empty list in case NPI does not exist in the CMS National Plan and Provider Enumeration System (NPPES) Registry.

                
    //--------------------------------------------------------------------------------------
    // Perform "getcode" operation to get healthcare provider information using NPI number.
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/getcode?q=1285636522&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "NPI": [
        {
          "NPI": "1285636522",
          "EntityType": "Organization",
          "EIN": "N/A",
          "IsOrgSubpart": "N",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER, INC",
          "FirstLineMailingAddress": "PO BOX 418283",
          "MailingAddressCityName": "BOSTON",
          "MailingAddressStateName": "MA",
          "MailingAddressPostalCode": "02241-8283",
          "MailingAddressCountryCode": "US",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400",
          "EnumerationDate": "06/01/2005",
          "LastUpdateDate": "11/25/2011",
          "AuthorizedOfficialLastName": "SCHNEIDER",
          "AuthorizedOfficialFirstName": "STEPHANIE",
          "AuthorizedOfficialTitle": "VP",
          "AuthorizedOfficialTelephoneNumber": "703-558-1403",
          "TaxonomyCode1": "207R00000X",
          "Taxonomy1": "Internal Medicine",
          "LicenseNumber1": "=========",
          "LicenseNumberStateCode1": "DC",
          "PrimaryTaxonomySwitch1": "Y",
          "OtherIdentifier1": "W677",
          "OtherIdentifierType1": "OTHER",
          "OtherIdentifierState1": "DC",
          "OtherIdentifierIssuer1": "BLUE SHIELD ADULT PCP GRP",
          "OtherIdentifier2": "027174100",
          "OtherIdentifierType2": "MEDICAID",
          "OtherIdentifierState2": "DC",
          "OtherIdentifier3": "097005100",
          "OtherIdentifierType3": "MEDICAID",
          "OtherIdentifierState3": "MD",
          "OtherIdentifier4": "442AGE",
          "OtherIdentifierType4": "OTHER",
          "OtherIdentifierState4": "MD",
          "OtherIdentifierIssuer4": "BLUE SHIELD PEDS PCP GRP#",
          "OtherIdentifier5": "6572",
          "OtherIdentifierType5": "OTHER",
          "OtherIdentifierState5": "DC",
          "OtherIdentifierIssuer5": "BLUE SHIELD GROUP NUMBER",
          "OtherIdentifier6": "W675",
          "OtherIdentifierType6": "OTHER",
          "OtherIdentifierState6": "DC",
          "OtherIdentifierIssuer6": "BLUE SHIELD PEDS PCP GRP#",
          "HealthcareProviderTaxonomyGroup1": "193200000X MULTI-SPECIALTY GROUP",
          "HealthcareProviderTaxonomyGroupDescription1": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization."
        }
      ]
    }
    Done. Press any key to exit ...
                
            

Use Case #3 - I Need to Get Multiple Healthcare Providers Using List of NPI Numbers

You may need to perform bulk search for performance optimization. The "getcodes" operation allows you to decrease number of round trips in orders of magnitude. For instance you can get information about hundred NPI in one REST call, instead of sending NPI numbers one-by-one.

                
    //--------------------------------------------------------------------------------------
    // Perform "getcodes" operation to get multiple healthcare providers using list of NPIs. 
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/getcodes?q=1285636522,1730198755,1427145176&rt=minjson&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "NPI": [
        {
          "NPI": "1285636522",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER, INC",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400"
        },
        {
          "NPI": "1730198755",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400"
        },
        {
          "NPI": "1427145176",
          "OrgName": "MEDSTAR - GEORGETOWN MEDICAL CENTER, INC.",
          "OtherOrgName": "GEORGETOWN UNIVERSITY HOSPITAL",
          "OtherOrgNameTypeCode": "3",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD., NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "202-444-3000",
          "PracticeLocationAddressFaxNumber": "202-444-3095"
        }
      ]
    }
    Done. Press any key to exit ...
                
            

Use Case #4 - I Need to Check NPI Number Status

Again, very common scenario. You just need to check NPI number status. It is simple. Take a look at the code below. Expected result contains requested NPI number, status, and short status description.

                
    //--------------------------------------------------------------------------------------
    // Perform "check_status" operation to get NPI Number status (active, deactivated, etc).
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/check_status?q=1285636522&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "Code": "1285636522",
      "Status": "Active",
      "Message": "\"1285636522\" NPI Number does exist and has \"active\" status"
    }
                
    Done. Press any key to exit ...
                
            

Use Case #5 - I need to retrieve a list of healthcare providers based on specified search parameters.

The system allows users to retrieve a list of healthcare providers by filtering on specified fields (e.g., organization name, state, city, ZIP code, etc.). The example below demonstrates how to retrieve all providers with a specified city, state, and ZIP code.

                
    //--------------------------------------------------------------------------------------
    // Perform "search_with_predicates" operation to get multiple healthcare providers using specified city, state, and ZIP code. 
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/search_with_predicates?q=&qf=City:true:REDMOND&qf=State:true:OR&qf=Zip:true:97756-9069&rt=json&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
{
  "NPI": [
    {
      "NPI": "1083349906",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "STAFFORD",
      "FirstName": "KADY",
      "NamePrefix": "MS.",
      "Credential": "LPC",
      "FirstLineMailingAddress": "13574 SW HIGHWAY 126",
      "MailingAddressCityName": "POWELL BUTTE",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97753-1541",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-480-6360",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-203-0307",
      "EnumerationDate": "07/24/2022",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional Counselor",
      "LicenseNumber1": "LPC6225",
      "LicenseNumberStateCode1": "ID",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C9084",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1215724679",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "SCHAY",
      "FirstName": "ANGELICA",
      "MiddleName": "NICOLE",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1841",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1841",
      "EnumerationDate": "04/21/2025",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101Y00000X",
      "Taxonomy1": "Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101Y00000X",
      "PrimaryTaxonomy": "Counselor"
    },
    {
      "NPI": "1013556505",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "IVENS",
      "FirstName": "KRYSTA",
      "FirstLineMailingAddress": "743 NW QUINCE AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-1250",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "360-526-1448",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "971-217-6150",
      "EnumerationDate": "12/31/2019",
      "LastUpdateDate": "02/15/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C7963",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "02/15/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1497336275",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "ARANT",
      "FirstName": "ERIN",
      "MiddleName": "HENNESSEY",
      "FirstLineMailingAddress": "4639 SW 37TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-6776",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "04/14/2021",
      "LastUpdateDate": "04/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "225X00000X",
      "Taxonomy1": "Occupational Therapist",
      "LicenseNumber1": "390047",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/14/2021",
      "PrimaryTaxonomyCode": "225X00000X",
      "PrimaryTaxonomy": "Occupational Therapist"
    },
    {
      "NPI": "1174191407",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "GRIMALT",
      "FirstName": "EUGENIA",
      "MiddleName": "N",
      "Credential": "PT",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1848",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "06/14/2021",
      "LastUpdateDate": "06/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "2251P0200X",
      "Taxonomy1": "Pediatric Physical Therapist",
      "LicenseNumber1": "63979",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization.",
      "CertificationDate": "06/14/2021",
      "PrimaryTaxonomyCode": "2251P0200X",
      "PrimaryTaxonomy": "Pediatric Physical Therapist"
    },
    {
      "NPI": "1912604117",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "PAINTER",
      "FirstName": "JENNIFER",
      "FirstLineMailingAddress": "20080 DOANNA WAY UNIT 3",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97702-2931",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "209-743-9813",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "02/08/2023",
      "LastUpdateDate": "02/08/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "02/08/2023",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1396434700",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "GROVE",
      "FirstName": "JENNIFER",
      "MiddleName": "RHEA",
      "FirstLineMailingAddress": "303 NW BROADWAY ST",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97703-2658",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "801-573-6047",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "801-573-6047",
      "EnumerationDate": "05/02/2023",
      "LastUpdateDate": "05/02/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "1041C0700X",
      "Taxonomy1": "Clinical Social Worker",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "05/02/2023",
      "PrimaryTaxonomyCode": "1041C0700X",
      "PrimaryTaxonomy": "Clinical Social Worker"
    },
    {
      "NPI": "1407698970",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "REDDEN",
      "FirstName": "SHANNON",
      "Credential": "CHW",
      "OtherLastName": "MCDOUGALL",
      "OtherFirstName": "SHANNON",
      "OtherLastNameTypeCode": "1",
      "FirstLineMailingAddress": "2312 NE 5TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-8488",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-460-2192",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "PracticeLocationAddressFaxNumber": "541-550-7956",
      "EnumerationDate": "06/06/2024",
      "LastUpdateDate": "06/06/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "172V00000X",
      "Taxonomy1": "Community Health Worker",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "06/06/2024",
      "PrimaryTaxonomyCode": "172V00000X",
      "PrimaryTaxonomy": "Community Health Worker"
    },
    {
      "NPI": "1942022256",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "JACQUOT",
      "FirstName": "SHAYLA",
      "FirstLineMailingAddress": "PO BOX 1397",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97709-1397",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1848",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "10/28/2024",
      "LastUpdateDate": "10/28/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "10/26/2024",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1912723131",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "WEIMER",
      "FirstName": "ALAYNA",
      "FirstLineMailingAddress": "2748 NW 19TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-7766",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-499-8292",
      "EnumerationDate": "12/03/2024",
      "LastUpdateDate": "12/03/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "171M00000X",
      "Taxonomy1": "Case Manager/Care Coordinator",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "12/03/2024",
      "PrimaryTaxonomyCode": "171M00000X",
      "PrimaryTaxonomy": "Case Manager/Care Coordinator"
    },
    {
      "NPI": "1790594125",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "WIDDER",
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      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "175T00000X",
      "Taxonomy1": "Peer Specialist",
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      "PrimaryTaxonomy": "Peer Specialist"
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    {
      "NPI": "1538965306",
      "EntityType": "Individual",
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      "MiddleName": "JEWELL",
      "FirstLineMailingAddress": "2821 SW 28TH ST",
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      "MailingAddressStateName": "OR",
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      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "760-927-4761",
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      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "02/21/2025",
      "LastUpdateDate": "02/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "175T00000X",
      "Taxonomy1": "Peer Specialist",
      "LicenseNumber1": "113398",
      "LicenseNumberStateCode1": "OR",
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      "CertificationDate": "02/21/2025",
      "PrimaryTaxonomyCode": "175T00000X",
      "PrimaryTaxonomy": "Peer Specialist"
    }
  ]
}
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