RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (14 ms elapsed)

{
  "NDC": [
    {
      "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": "27281-001-96",
      "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": "27281-008-96",
      "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": "27281-009-96",
      "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": "27281-011-96",
      "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": "11084-010-96",
      "PackageDescription": ".296 L in 1 BOTTLE, PLASTIC (11084-010-96) ",
      "NDC11Code": "11084-0010-96",
      "ProductNDC": "11084-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Refresh Antibac Foam",
      "NonProprietaryName": "Benzalkonium Chloride",
      "DosageFormName": "SOAP",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20170612",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "505G(a)(3)",
      "LabelerName": "SC Johnson Professional USA, Inc.",
      "SubstanceName": "BENZALKONIUM CHLORIDE",
      "StrengthNumber": ".13",
      "StrengthUnit": "g/L",
      "Status": "Deprecated",
      "LastUpdate": "2025-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20190801",
      "EndMarketingDatePackage": "20241231",
      "SamplePackage": "N",
      "IndicationAndUsage": "for handwashing to reduce bacteria on the skin."
    },
    {
      "NDCCode": "25373-010-07",
      "PackageDescription": "96 L in 1 CYLINDER (25373-010-07) ",
      "NDC11Code": "25373-0010-07",
      "ProductNDC": "25373-010",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Helium",
      "NonProprietaryName": "Helium",
      "DosageFormName": "GAS",
      "RouteName": "RESPIRATORY (INHALATION)",
      "StartMarketingDate": "19901127",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA206826",
      "LabelerName": "Linde Gas & Equipment Inc.",
      "SubstanceName": "HELIUM",
      "StrengthNumber": "99",
      "StrengthUnit": "L/100L",
      "Status": "Deprecated",
      "LastUpdate": "2023-01-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20221231",
      "StartMarketingDatePackage": "19901127",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "50425-010-96",
      "PackageDescription": "472 mL in 1 BOTTLE (50425-010-96) ",
      "NDC11Code": "50425-0010-96",
      "ProductNDC": "50425-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Scrub Care Povidone Iodine Cleansing Scrub",
      "NonProprietaryName": "Povidone Iodine",
      "DosageFormName": "SOLUTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20010101",
      "EndMarketingDate": "20240229",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "505G(a)(3)",
      "LabelerName": "CareFusion 213 LLC",
      "SubstanceName": "POVIDONE-IODINE",
      "StrengthNumber": "7.5",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2024-03-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20150119",
      "EndMarketingDatePackage": "20240229",
      "SamplePackage": "N",
      "IndicationAndUsage": ": 1 Surgical Hand Scrub: Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care. , 2 Patient Preoperative Skin Preparation: for preparation of skin prior to surgery.Helps reduce bacteria that potentially can cause skin infection. , 3 Antiseptic Handwash: for hand washing to reduce bacteria on skin ."
    },
    {
      "NDCCode": "58406-010-96",
      "PackageDescription": "1 SYRINGE in 1 CARTON (58406-010-96)  / .5 mL in 1 SYRINGE",
      "NDC11Code": "58406-0010-96",
      "ProductNDC": "58406-010",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Enbrel",
      "NonProprietaryName": "Etanercept",
      "DosageFormName": "SOLUTION",
      "RouteName": "SUBCUTANEOUS",
      "StartMarketingDate": "20190607",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA103795",
      "LabelerName": "Immunex Corporation",
      "SubstanceName": "ETANERCEPT",
      "StrengthNumber": "25",
      "StrengthUnit": "mg/.5mL",
      "Pharm_Classes": "Tumor Necrosis Factor Blocker [EPC], Tumor Necrosis Factor Receptor Blocking Activity [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-05-20",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20190607",
      "SamplePackage": "Y",
      "IndicationAndUsage": "Enbrel is a tumor necrosis factor (TNF) blocker indicated for the treatment of. Adult patients with: 1 Rheumatoid Arthritis (RA) (1.1), 2 Psoriatic Arthritis (PsA) (1.3), 3 Ankylosing Spondylitis (AS) (1.4), 4 Plaque Psoriasis (PsO) (1.5).",
      "Description": "Etanercept, a tumor necrosis factor (TNF) blocker, is a dimeric fusion protein consisting of the extracellular ligand-binding portion of the human 75 kilodalton (p75) tumor necrosis factor receptor (TNFR) linked to the Fc portion of human IgG1. The Fc component of etanercept contains the CH2 domain, the CH3 domain and hinge region, but not the CH1 domain of IgG1. Etanercept is produced by recombinant DNA technology in a Chinese hamster ovary (CHO) mammalian cell expression system. It consists of 934 amino acids and has an apparent molecular weight of approximately 150 kilodaltons. Enbrel (etanercept) Injection in the single-dose prefilled syringe, the single-dose prefilled SureClick autoinjector and the single-dose vial is clear and colorless, sterile, preservative-free solution, and is formulated at pH 6.3 ± 0.2. Enbrel (etanercept) for Injection is supplied in a multiple-dose vial as a sterile, white, preservative-free, lyophilized powder. Reconstitution with 1 mL of the supplied Sterile Bacteriostatic Water for Injection, USP (containing 0.9% benzyl alcohol) yields a multiple-dose, clear, and colorless solution 1 mL containing 25 mg of Enbrel, with a pH of 7.4 ± 0.3. Enbrel (etanercept) Injection in the Enbrel Mini single-dose prefilled cartridge for use with the AutoTouch reusable autoinjector is clear and colorless, sterile, preservative-free solution, and is formulated at pH 6.3 ± 0.2."
    },
    {
      "NDCCode": "63323-010-96",
      "PackageDescription": "25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96)  / 20 mL in 1 VIAL, MULTI-DOSE",
      "NDC11Code": "63323-0010-96",
      "ProductNDC": "63323-010",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Gentamicin",
      "NonProprietaryName": "Gentamicin Sulfate",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
      "StartMarketingDate": "20000810",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA062366",
      "LabelerName": "Fresenius Kabi USA, LLC",
      "SubstanceName": "GENTAMICIN SULFATE",
      "StrengthNumber": "40",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS]",
      "Status": "Active",
      "LastUpdate": "2024-10-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20000810",
      "SamplePackage": "N",
      "IndicationAndUsage": "To reduce the development of drug-resistant bacteria and maintain the effectiveness of Gentamicin Injection, USP and other antibacterial drugs, Gentamicin Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.  When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy.  In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Gentamicin Injection, USP is indicated in the treatment of serious infections caused by susceptible strains of the following microorganisms: Pseudomonas aeruginosa, Proteus species (indole-positive and indole-negative), Escherichia coli, Klebsiella-Enterobacter-Serratia species, Citrobacter species and Staphylococcus species (coagulase-positive and coagulase-negative). Clinical studies have shown gentamicin injection to be effective in bacterial neonatal sepsis; bacterial septicemia and serious bacterial infections of the central nervous system (meningitis), urinary tract, respiratory tract, gastrointestinal tract (including peritonitis), skin, bone and soft tissue (including burns).  Aminoglycosides, including gentamicin, are not indicated in uncomplicated initial episodes of urinary tract infections unless the causative organisms are susceptible to these antibiotics and are not susceptible to antibiotics having less potential for toxicity. Specimens for bacterial culture should be obtained to isolate and identify causative organisms and to determine their susceptibility to gentamicin. Gentamicin injection may be considered as initial therapy in suspected or confirmed gram-negative infections, and therapy may be instituted before obtaining results of susceptibility testing.  The decision to continue therapy with this drug should be based on the results of susceptibility tests, the severity of the infection and the important additional concepts contained in the boxed WARNINGS.   If the causative organisms are resistant to gentamicin, other appropriate therapy should be instituted. In serious infections when the causative organisms are unknown, gentamicin injection may be administered as initial therapy in conjunction with a penicillin-type or cephalosporin-type drug before obtaining results of susceptibility testing.  If anaerobic organisms are suspected as etiologic agents, consideration should be given to using other suitable antimicrobial therapy in conjunction with gentamicin.  Following identification of the organism and its susceptibility, appropriate antibiotic therapy should then be continued. Gentamicin injection has been used effectively in combination with carbenicillin for the treatment of life-threatening infections caused by Pseudomonas aeruginosa.  It has also been found effective when used in conjunction with a penicillin-type drug for treatment of endocarditis caused by group D streptococci. Gentamicin injection has also been shown to be effective in the treatment of serious staphylococcal infections.  While not the antibiotic of first choice, gentamicin injection may be considered when penicillins or other less potentially toxic drugs are contraindicated and bacterial susceptibility tests and clinical judgment indicate its use.  It may also be considered in mixed infections caused by susceptible strains of staphylococci and gram-negative organisms. In the neonate with suspected bacterial sepsis or staphylococcal pneumonia, a penicillin-type drug is also usually indicated as concomitant therapy with gentamicin.",
      "Description": "Gentamicin sulfate, a water-soluble antibiotic of the aminoglycoside group, is derived by the growth of Micromonospora purpurea, an actinomycete. It has the following structural formula. Gentamicin injection is a sterile, nonpyrogenic aqueous solution for parenteral administration. Each mL contains: Gentamicin sulfate equivalent to 40 mg gentamicin, methylparaben 1.8 mg and propylparaben 0.2 mg as preservatives, sodium metabisulfite 3.2 mg and edetate disodium 0.1 mg, Water for Injection q.s.  Sodium hydroxide and/or sulfuric acid may have been added for pH adjustment."
    },
    {
      "NDCCode": "67777-010-03",
      "PackageDescription": "96 BOX in 1 CASE (67777-010-03)  / 24 BOTTLE in 1 BOX (67777-010-15)  / 118.3 mL in 1 BOTTLE (67777-010-14) ",
      "NDC11Code": "67777-0010-03",
      "ProductNDC": "67777-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sannytize Hand Sanitizer",
      "NonProprietaryName": "Hand Sanitizer",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20191101",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M003",
      "LabelerName": "Dynarex Corporation",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "70",
      "StrengthUnit": "mL/100mL",
      "Status": "Active",
      "LastUpdate": "2024-01-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20191101",
      "SamplePackage": "N",
      "IndicationAndUsage": "For hand washing to decrease bacteria on the skin. ."
    },
    {
      "NDCCode": "72683-010-01",
      "PackageDescription": "96 g in 1 BOTTLE (72683-010-01) ",
      "NDC11Code": "72683-0010-01",
      "ProductNDC": "72683-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Roll Pain Away Lavender",
      "NonProprietaryName": "Capsaicin",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20260617",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M017",
      "LabelerName": "PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA",
      "SubstanceName": "CAPSAICIN",
      "StrengthNumber": ".025",
      "StrengthUnit": "g/100g",
      "Status": "Active",
      "LastUpdate": "2026-06-19",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260617",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves minor aches and pains of muscles and joints associated with: 1 arthritis, 2 simple backache, 3 strains, 4 sprains, 5 bruises."
    },
    {
      "NDCCode": "73143-010-03",
      "PackageDescription": "96 g in 1 CAN (73143-010-03) ",
      "NDC11Code": "73143-0010-03",
      "ProductNDC": "73143-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Menthol",
      "NonProprietaryName": "Menthol",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20190718",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "Jag Alliance, LLC",
      "SubstanceName": "MENTHOL, UNSPECIFIED FORM",
      "StrengthNumber": "10",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2022-01-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20190718",
      "SamplePackage": "N",
      "IndicationAndUsage": "Aid for temporary local relief of minor pain in muscles or joints."
    },
    {
      "NDCCode": "80808-010-86",
      "PackageDescription": "12 CANISTER in 1 CARTON (80808-010-86)  > 160 PATCH in 1 CANISTER (80808-010-96)  > 5 mL in 1 PATCH (80808-010-16) ",
      "NDC11Code": "80808-0010-86",
      "ProductNDC": "80808-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Hygenize Alcohol Wipes",
      "NonProprietaryName": "Alcohol",
      "DosageFormName": "PATCH",
      "RouteName": "EXTRACORPOREAL",
      "StartMarketingDate": "20201004",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part333E",
      "LabelerName": "Hygenize Corp.",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "70",
      "StrengthUnit": "mL/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-12-18",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20201004",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "83176-010-01",
      "PackageDescription": "96 g in 1 BOTTLE (83176-010-01) ",
      "NDC11Code": "83176-0010-01",
      "ProductNDC": "83176-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Oheal Manuka Honey Eczema Cream",
      "NonProprietaryName": "Manuka Honey Eczema Cream",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20230610",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "M005",
      "LabelerName": "Dr.luke Healthcare LLC",
      "SubstanceName": "CLOTRIMAZOLE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/100g",
      "Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2023-06-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20230610",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "10631-010-30",
      "PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-010-30) ",
      "NDC11Code": "10631-0010-30",
      "ProductNDC": "10631-010",
      "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": "100",
      "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": "63304-010-30",
      "PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-010-30) ",
      "NDC11Code": "63304-0010-30",
      "ProductNDC": "63304-010",
      "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": "100",
      "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": "71597-010-02",
      "PackageDescription": "1 TUBE in 1 CARTON (71597-010-02)  > 50 mL in 1 TUBE (71597-010-01)",
      "NDC11Code": "71597-0010-02",
      "ProductNDC": "71597-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Acwell Sensitive Solu Tion Sun Control",
      "NonProprietaryName": "Zinc Oxide, Titanium Dioxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20170701",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "BNHCOSMETICS CO.,LTD.",
      "SubstanceName": "ZINC OXIDE; TITANIUM DIOXIDE",
      "StrengthNumber": "6.96; 3.99",
      "StrengthUnit": "g/50mL; g/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-11-30",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "74157-010-30",
      "PackageDescription": "1 BOTTLE in 1 CARTON (74157-010-30)  / 30 TABLET, DELAYED RELEASE in 1 BOTTLE",
      "NDC11Code": "74157-0010-30",
      "ProductNDC": "74157-010",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Prednisone Delayed Release",
      "NonProprietaryName": "Prednisone",
      "DosageFormName": "TABLET, DELAYED RELEASE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20251215",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA219477",
      "LabelerName": "INA Pharmaceutics Inc",
      "SubstanceName": "PREDNISONE",
      "StrengthNumber": "1",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
      "Status": "Active",
      "LastUpdate": "2025-12-20",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20251215",
      "SamplePackage": "N",
      "IndicationAndUsage": "Prednisone delayed-release tablets are indicated in the treatment of the following diseases or conditions.",
      "Description": "The active ingredient in prednisone delayed-release tablet is prednisone (a corticosteroid). Corticosteroids are adrenocortical steroids, both naturally occurring and synthetic. The molecular formula for prednisone is C 21H 26O 5. The chemical name for prednisone is 17,21-dihydroxypregna-1,4-diene-3,11,20-trione, and the structural formula is:. Prednisone, USP is a white to practically white crystalline powder and has a molecular weight of 358.44 g/mol. Prednisone, USP is practically insoluble in water, slightly soluble in ethanol (96 per cent) and in methylene chloride. Prednisone delayed-release tablet is a delayed-release prednisone tablet. It consists of a prednisone-containing core tablet in an inactive shell, which delays the onset of in vitro drug dissolution by approximately 4 hours. Each tablet contains 1 mg, or 2 mg of prednisone, USP with the following inactive ingredients: dibasic calcium phosphate dihydrate, colloidal silicon dioxide, croscarmellose sodium, glycerol dibehenate, lactose monohydrate, magnesium stearate, povidone, yellow ferric oxide and red ferric oxide. Each prednisone delayed-release tablet contains 30 mg of phosphorous. Each prednisone delayed-release tablet contains less than 5 mg of sodium."
    },
    {
      "NDCCode": "76296-010-40",
      "PackageDescription": "1 BOTTLE in 1 CARTON (76296-010-40)  > 40 mL in 1 BOTTLE",
      "NDC11Code": "76296-0010-40",
      "ProductNDC": "76296-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Vinoperfect Broad Spectrum Spf 15 Day Perfecting Fluid",
      "NonProprietaryName": "Avobenzone, Octinoxate, Octisalate, Octocrylene",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20140306",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Caudalie USA Inc.",
      "SubstanceName": "AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE",
      "StrengthNumber": "30; 39.96; 50; 80",
      "StrengthUnit": "mg/mL; mg/mL; mg/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2016-12-06"
    },
    {
      "NDCCode": "85951-010-01",
      "PackageDescription": "1 g in 1 TUBE (85951-010-01) ",
      "NDC11Code": "85951-0010-01",
      "ProductNDC": "85951-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Eczema Therapy",
      "NonProprietaryName": "Colloidal Oatmeal",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20250806",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M016",
      "LabelerName": "SilverCeuticals",
      "SubstanceName": "OATMEAL",
      "StrengthNumber": ".96",
      "StrengthUnit": "g/96g",
      "Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2026-05-15",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20250806",
      "SamplePackage": "N",
      "IndicationAndUsage": "Directions: 1 Clean the affected area, 2 Apply a small amount of this product on the area once daily, 3 May be covered with a sterile bandage, 4 If bandaged, let dry first."
    },
    {
      "NDCCode": "85951-010-34",
      "PackageDescription": "1 g in 1 BOTTLE, DISPENSING (85951-010-34) ",
      "NDC11Code": "85951-0010-34",
      "ProductNDC": "85951-010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Eczema Therapy",
      "NonProprietaryName": "Colloidal Oatmeal",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20250806",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M016",
      "LabelerName": "SilverCeuticals",
      "SubstanceName": "OATMEAL",
      "StrengthNumber": ".96",
      "StrengthUnit": "g/96g",
      "Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2026-05-15",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20250806",
      "SamplePackage": "N",
      "IndicationAndUsage": "Directions: 1 Clean the affected area, 2 Apply a small amount of this product on the area once daily, 3 May be covered with a sterile bandage, 4 If bandaged, let dry first."
    },
    {
      "NDCCode": "99207-010-10",
      "PackageDescription": "1 BOTTLE, PLASTIC in 1 CARTON (99207-010-10)  > 120 mL in 1 BOTTLE, PLASTIC",
      "NDC11Code": "99207-0010-10",
      "ProductNDC": "99207-010",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Loprox",
      "NonProprietaryName": "Ciclopirox",
      "DosageFormName": "SHAMPOO",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20030320",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA021159",
      "LabelerName": "Bausch Health US, LLC",
      "SubstanceName": "CICLOPIROX",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/.96mL",
      "Pharm_Classes": "Decreased DNA Replication [PE], Decreased Protein Synthesis [PE], Decreased RNA Replication [PE], Protein Synthesis Inhibitors [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20030320",
      "SamplePackage": "N",
      "IndicationAndUsage": "LOPROX® (ciclopirox) Shampoo, 1% is indicated for the topical treatment of seborrheic dermatitis of the scalp in adults.",
      "Description": "LOPROX (ciclopirox) Shampoo, 1% contains the synthetic antifungal agent ciclopirox for topical use. Each gram (equivalent to 0.96 mL) of LOPROX Shampoo contains 10 mg ciclopirox in a shampoo base consisting of disodium laureth sulfosuccinate, laureth-2, purified water, sodium chloride, and sodium laureth sulfate. LOPROX Shampoo is a colorless, translucent solution. The chemical name for ciclopirox is 6-cyclohexyl-1-hydroxy-4-methyl-2(1H)-pyridone, with the empirical formula C12H17NO2 and a molecular weight of 207.27. The CAS Registry Number is [29342-05-0]. The chemical structure is."
    },
    {
      "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."
    }
  ]
}
                    

{"NDC":[{"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":"27281-001-96","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":"27281-008-96","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":"27281-009-96","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":"27281-011-96","ProprietaryName":"Lung Detox","NonProprietaryName":"Silver Nitrate, Arsenic Trioxide, Activated Charcoal, Silybum Marianum Seed, Herring Sperm Dna, Pork Liver, Mercuric Chloride, Lead"},{"NDCCode":"11084-010-96","ProprietaryName":"Refresh Antibac Foam","NonProprietaryName":"Benzalkonium Chloride"},{"NDCCode":"25373-010-07","ProprietaryName":"Helium","NonProprietaryName":"Helium"},{"NDCCode":"50425-010-96","ProprietaryName":"Scrub Care Povidone Iodine Cleansing Scrub","NonProprietaryName":"Povidone Iodine"},{"NDCCode":"58406-010-96","ProprietaryName":"Enbrel","NonProprietaryName":"Etanercept"},{"NDCCode":"63323-010-96","ProprietaryName":"Gentamicin","NonProprietaryName":"Gentamicin Sulfate"},{"NDCCode":"67777-010-03","ProprietaryName":"Sannytize Hand Sanitizer","NonProprietaryName":"Hand Sanitizer"},{"NDCCode":"72683-010-01","ProprietaryName":"Roll Pain Away Lavender","NonProprietaryName":"Capsaicin"},{"NDCCode":"73143-010-03","ProprietaryName":"Menthol","NonProprietaryName":"Menthol"},{"NDCCode":"80808-010-86","ProprietaryName":"Hygenize Alcohol Wipes","NonProprietaryName":"Alcohol"},{"NDCCode":"83176-010-01","ProprietaryName":"Oheal Manuka Honey Eczema Cream","NonProprietaryName":"Manuka Honey Eczema Cream"},{"NDCCode":"10631-010-30","ProprietaryName":"Kapspargo","NonProprietaryName":"Metoprolol Succinate"},{"NDCCode":"63304-010-30","ProprietaryName":"Metoprolol Succinate","NonProprietaryName":"Metoprolol Succinate"},{"NDCCode":"71597-010-02","ProprietaryName":"Acwell Sensitive Solu Tion Sun Control","NonProprietaryName":"Zinc Oxide, Titanium Dioxide"},{"NDCCode":"74157-010-30","ProprietaryName":"Prednisone Delayed Release","NonProprietaryName":"Prednisone"},{"NDCCode":"76296-010-40","ProprietaryName":"Vinoperfect Broad Spectrum Spf 15 Day Perfecting Fluid","NonProprietaryName":"Avobenzone, Octinoxate, Octisalate, Octocrylene"},{"NDCCode":"85951-010-01","ProprietaryName":"Eczema Therapy","NonProprietaryName":"Colloidal Oatmeal"},{"NDCCode":"85951-010-34","ProprietaryName":"Eczema Therapy","NonProprietaryName":"Colloidal Oatmeal"},{"NDCCode":"99207-010-10","ProprietaryName":"Loprox","NonProprietaryName":"Ciclopirox"},{"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"}]}
                    

<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <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>27281-001-96</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>27281-008-96</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>27281-009-96</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>27281-011-96</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>11084-010-96</NDCCode>
    <PackageDescription>.296 L in 1 BOTTLE, PLASTIC (11084-010-96) </PackageDescription>
    <NDC11Code>11084-0010-96</NDC11Code>
    <ProductNDC>11084-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Refresh Antibac Foam</ProprietaryName>
    <NonProprietaryName>Benzalkonium Chloride</NonProprietaryName>
    <DosageFormName>SOAP</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20170612</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>505G(a)(3)</ApplicationNumber>
    <LabelerName>SC Johnson Professional USA, Inc.</LabelerName>
    <SubstanceName>BENZALKONIUM CHLORIDE</SubstanceName>
    <StrengthNumber>.13</StrengthNumber>
    <StrengthUnit>g/L</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2025-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190801</StartMarketingDatePackage>
    <EndMarketingDatePackage>20241231</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>for handwashing to reduce bacteria on the skin.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>25373-010-07</NDCCode>
    <PackageDescription>96 L in 1 CYLINDER (25373-010-07) </PackageDescription>
    <NDC11Code>25373-0010-07</NDC11Code>
    <ProductNDC>25373-010</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Helium</ProprietaryName>
    <NonProprietaryName>Helium</NonProprietaryName>
    <DosageFormName>GAS</DosageFormName>
    <RouteName>RESPIRATORY (INHALATION)</RouteName>
    <StartMarketingDate>19901127</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA206826</ApplicationNumber>
    <LabelerName>Linde Gas &amp; Equipment Inc.</LabelerName>
    <SubstanceName>HELIUM</SubstanceName>
    <StrengthNumber>99</StrengthNumber>
    <StrengthUnit>L/100L</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2023-01-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20221231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>19901127</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>50425-010-96</NDCCode>
    <PackageDescription>472 mL in 1 BOTTLE (50425-010-96) </PackageDescription>
    <NDC11Code>50425-0010-96</NDC11Code>
    <ProductNDC>50425-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Scrub Care Povidone Iodine Cleansing Scrub</ProprietaryName>
    <NonProprietaryName>Povidone Iodine</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20010101</StartMarketingDate>
    <EndMarketingDate>20240229</EndMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>505G(a)(3)</ApplicationNumber>
    <LabelerName>CareFusion 213 LLC</LabelerName>
    <SubstanceName>POVIDONE-IODINE</SubstanceName>
    <StrengthNumber>7.5</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-03-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20150119</StartMarketingDatePackage>
    <EndMarketingDatePackage>20240229</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>: 1 Surgical Hand Scrub: Significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care. , 2 Patient Preoperative Skin Preparation: for preparation of skin prior to surgery.Helps reduce bacteria that potentially can cause skin infection. , 3 Antiseptic Handwash: for hand washing to reduce bacteria on skin .</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>58406-010-96</NDCCode>
    <PackageDescription>1 SYRINGE in 1 CARTON (58406-010-96)  / .5 mL in 1 SYRINGE</PackageDescription>
    <NDC11Code>58406-0010-96</NDC11Code>
    <ProductNDC>58406-010</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Enbrel</ProprietaryName>
    <NonProprietaryName>Etanercept</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20190607</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA103795</ApplicationNumber>
    <LabelerName>Immunex Corporation</LabelerName>
    <SubstanceName>ETANERCEPT</SubstanceName>
    <StrengthNumber>25</StrengthNumber>
    <StrengthUnit>mg/.5mL</StrengthUnit>
    <Pharm_Classes>Tumor Necrosis Factor Blocker [EPC], Tumor Necrosis Factor Receptor Blocking Activity [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-05-20</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190607</StartMarketingDatePackage>
    <SamplePackage>Y</SamplePackage>
    <IndicationAndUsage>Enbrel is a tumor necrosis factor (TNF) blocker indicated for the treatment of. Adult patients with: 1 Rheumatoid Arthritis (RA) (1.1), 2 Psoriatic Arthritis (PsA) (1.3), 3 Ankylosing Spondylitis (AS) (1.4), 4 Plaque Psoriasis (PsO) (1.5).</IndicationAndUsage>
    <Description>Etanercept, a tumor necrosis factor (TNF) blocker, is a dimeric fusion protein consisting of the extracellular ligand-binding portion of the human 75 kilodalton (p75) tumor necrosis factor receptor (TNFR) linked to the Fc portion of human IgG1. The Fc component of etanercept contains the CH2 domain, the CH3 domain and hinge region, but not the CH1 domain of IgG1. Etanercept is produced by recombinant DNA technology in a Chinese hamster ovary (CHO) mammalian cell expression system. It consists of 934 amino acids and has an apparent molecular weight of approximately 150 kilodaltons. Enbrel (etanercept) Injection in the single-dose prefilled syringe, the single-dose prefilled SureClick autoinjector and the single-dose vial is clear and colorless, sterile, preservative-free solution, and is formulated at pH 6.3 ± 0.2. Enbrel (etanercept) for Injection is supplied in a multiple-dose vial as a sterile, white, preservative-free, lyophilized powder. Reconstitution with 1 mL of the supplied Sterile Bacteriostatic Water for Injection, USP (containing 0.9% benzyl alcohol) yields a multiple-dose, clear, and colorless solution 1 mL containing 25 mg of Enbrel, with a pH of 7.4 ± 0.3. Enbrel (etanercept) Injection in the Enbrel Mini single-dose prefilled cartridge for use with the AutoTouch reusable autoinjector is clear and colorless, sterile, preservative-free solution, and is formulated at pH 6.3 ± 0.2.</Description>
  </NDC>
  <NDC>
    <NDCCode>63323-010-96</NDCCode>
    <PackageDescription>25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-96)  / 20 mL in 1 VIAL, MULTI-DOSE</PackageDescription>
    <NDC11Code>63323-0010-96</NDC11Code>
    <ProductNDC>63323-010</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Gentamicin</ProprietaryName>
    <NonProprietaryName>Gentamicin Sulfate</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAMUSCULAR; INTRAVENOUS</RouteName>
    <StartMarketingDate>20000810</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA062366</ApplicationNumber>
    <LabelerName>Fresenius Kabi USA, LLC</LabelerName>
    <SubstanceName>GENTAMICIN SULFATE</SubstanceName>
    <StrengthNumber>40</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-10-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20000810</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>To reduce the development of drug-resistant bacteria and maintain the effectiveness of Gentamicin Injection, USP and other antibacterial drugs, Gentamicin Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.  When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy.  In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Gentamicin Injection, USP is indicated in the treatment of serious infections caused by susceptible strains of the following microorganisms: Pseudomonas aeruginosa, Proteus species (indole-positive and indole-negative), Escherichia coli, Klebsiella-Enterobacter-Serratia species, Citrobacter species and Staphylococcus species (coagulase-positive and coagulase-negative). Clinical studies have shown gentamicin injection to be effective in bacterial neonatal sepsis; bacterial septicemia and serious bacterial infections of the central nervous system (meningitis), urinary tract, respiratory tract, gastrointestinal tract (including peritonitis), skin, bone and soft tissue (including burns).  Aminoglycosides, including gentamicin, are not indicated in uncomplicated initial episodes of urinary tract infections unless the causative organisms are susceptible to these antibiotics and are not susceptible to antibiotics having less potential for toxicity. Specimens for bacterial culture should be obtained to isolate and identify causative organisms and to determine their susceptibility to gentamicin. Gentamicin injection may be considered as initial therapy in suspected or confirmed gram-negative infections, and therapy may be instituted before obtaining results of susceptibility testing.  The decision to continue therapy with this drug should be based on the results of susceptibility tests, the severity of the infection and the important additional concepts contained in the boxed WARNINGS.   If the causative organisms are resistant to gentamicin, other appropriate therapy should be instituted. In serious infections when the causative organisms are unknown, gentamicin injection may be administered as initial therapy in conjunction with a penicillin-type or cephalosporin-type drug before obtaining results of susceptibility testing.  If anaerobic organisms are suspected as etiologic agents, consideration should be given to using other suitable antimicrobial therapy in conjunction with gentamicin.  Following identification of the organism and its susceptibility, appropriate antibiotic therapy should then be continued. Gentamicin injection has been used effectively in combination with carbenicillin for the treatment of life-threatening infections caused by Pseudomonas aeruginosa.  It has also been found effective when used in conjunction with a penicillin-type drug for treatment of endocarditis caused by group D streptococci. Gentamicin injection has also been shown to be effective in the treatment of serious staphylococcal infections.  While not the antibiotic of first choice, gentamicin injection may be considered when penicillins or other less potentially toxic drugs are contraindicated and bacterial susceptibility tests and clinical judgment indicate its use.  It may also be considered in mixed infections caused by susceptible strains of staphylococci and gram-negative organisms. In the neonate with suspected bacterial sepsis or staphylococcal pneumonia, a penicillin-type drug is also usually indicated as concomitant therapy with gentamicin.</IndicationAndUsage>
    <Description>Gentamicin sulfate, a water-soluble antibiotic of the aminoglycoside group, is derived by the growth of Micromonospora purpurea, an actinomycete. It has the following structural formula. Gentamicin injection is a sterile, nonpyrogenic aqueous solution for parenteral administration. Each mL contains: Gentamicin sulfate equivalent to 40 mg gentamicin, methylparaben 1.8 mg and propylparaben 0.2 mg as preservatives, sodium metabisulfite 3.2 mg and edetate disodium 0.1 mg, Water for Injection q.s.  Sodium hydroxide and/or sulfuric acid may have been added for pH adjustment.</Description>
  </NDC>
  <NDC>
    <NDCCode>67777-010-03</NDCCode>
    <PackageDescription>96 BOX in 1 CASE (67777-010-03)  / 24 BOTTLE in 1 BOX (67777-010-15)  / 118.3 mL in 1 BOTTLE (67777-010-14) </PackageDescription>
    <NDC11Code>67777-0010-03</NDC11Code>
    <ProductNDC>67777-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sannytize Hand Sanitizer</ProprietaryName>
    <NonProprietaryName>Hand Sanitizer</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20191101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M003</ApplicationNumber>
    <LabelerName>Dynarex Corporation</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>70</StrengthNumber>
    <StrengthUnit>mL/100mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-01-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20191101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For hand washing to decrease bacteria on the skin. .</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>72683-010-01</NDCCode>
    <PackageDescription>96 g in 1 BOTTLE (72683-010-01) </PackageDescription>
    <NDC11Code>72683-0010-01</NDC11Code>
    <ProductNDC>72683-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Roll Pain Away Lavender</ProprietaryName>
    <NonProprietaryName>Capsaicin</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20260617</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M017</ApplicationNumber>
    <LabelerName>PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA</LabelerName>
    <SubstanceName>CAPSAICIN</SubstanceName>
    <StrengthNumber>.025</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-06-19</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260617</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves minor aches and pains of muscles and joints associated with: 1 arthritis, 2 simple backache, 3 strains, 4 sprains, 5 bruises.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>73143-010-03</NDCCode>
    <PackageDescription>96 g in 1 CAN (73143-010-03) </PackageDescription>
    <NDC11Code>73143-0010-03</NDC11Code>
    <ProductNDC>73143-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Menthol</ProprietaryName>
    <NonProprietaryName>Menthol</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20190718</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>Jag Alliance, LLC</LabelerName>
    <SubstanceName>MENTHOL, UNSPECIFIED FORM</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2022-01-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190718</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Aid for temporary local relief of minor pain in muscles or joints.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>80808-010-86</NDCCode>
    <PackageDescription>12 CANISTER in 1 CARTON (80808-010-86)  &gt; 160 PATCH in 1 CANISTER (80808-010-96)  &gt; 5 mL in 1 PATCH (80808-010-16) </PackageDescription>
    <NDC11Code>80808-0010-86</NDC11Code>
    <ProductNDC>80808-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Hygenize Alcohol Wipes</ProprietaryName>
    <NonProprietaryName>Alcohol</NonProprietaryName>
    <DosageFormName>PATCH</DosageFormName>
    <RouteName>EXTRACORPOREAL</RouteName>
    <StartMarketingDate>20201004</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part333E</ApplicationNumber>
    <LabelerName>Hygenize Corp.</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>70</StrengthNumber>
    <StrengthUnit>mL/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-12-18</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20201004</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>83176-010-01</NDCCode>
    <PackageDescription>96 g in 1 BOTTLE (83176-010-01) </PackageDescription>
    <NDC11Code>83176-0010-01</NDC11Code>
    <ProductNDC>83176-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Oheal Manuka Honey Eczema Cream</ProprietaryName>
    <NonProprietaryName>Manuka Honey Eczema Cream</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20230610</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>M005</ApplicationNumber>
    <LabelerName>Dr.luke Healthcare LLC</LabelerName>
    <SubstanceName>CLOTRIMAZOLE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Pharm_Classes>Azole Antifungal [EPC], Azoles [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2023-06-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230610</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>10631-010-30</NDCCode>
    <PackageDescription>30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (10631-010-30) </PackageDescription>
    <NDC11Code>10631-0010-30</NDC11Code>
    <ProductNDC>10631-010</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>100</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>63304-010-30</NDCCode>
    <PackageDescription>30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-010-30) </PackageDescription>
    <NDC11Code>63304-0010-30</NDC11Code>
    <ProductNDC>63304-010</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>100</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>71597-010-02</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (71597-010-02)  &gt; 50 mL in 1 TUBE (71597-010-01)</PackageDescription>
    <NDC11Code>71597-0010-02</NDC11Code>
    <ProductNDC>71597-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Acwell Sensitive Solu Tion Sun Control</ProprietaryName>
    <NonProprietaryName>Zinc Oxide, Titanium Dioxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20170701</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>BNHCOSMETICS CO.,LTD.</LabelerName>
    <SubstanceName>ZINC OXIDE; TITANIUM DIOXIDE</SubstanceName>
    <StrengthNumber>6.96; 3.99</StrengthNumber>
    <StrengthUnit>g/50mL; g/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-11-30</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>74157-010-30</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (74157-010-30)  / 30 TABLET, DELAYED RELEASE in 1 BOTTLE</PackageDescription>
    <NDC11Code>74157-0010-30</NDC11Code>
    <ProductNDC>74157-010</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Prednisone Delayed Release</ProprietaryName>
    <NonProprietaryName>Prednisone</NonProprietaryName>
    <DosageFormName>TABLET, DELAYED RELEASE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20251215</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA219477</ApplicationNumber>
    <LabelerName>INA Pharmaceutics Inc</LabelerName>
    <SubstanceName>PREDNISONE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-12-20</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20251215</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Prednisone delayed-release tablets are indicated in the treatment of the following diseases or conditions.</IndicationAndUsage>
    <Description>The active ingredient in prednisone delayed-release tablet is prednisone (a corticosteroid). Corticosteroids are adrenocortical steroids, both naturally occurring and synthetic. The molecular formula for prednisone is C 21H 26O 5. The chemical name for prednisone is 17,21-dihydroxypregna-1,4-diene-3,11,20-trione, and the structural formula is:. Prednisone, USP is a white to practically white crystalline powder and has a molecular weight of 358.44 g/mol. Prednisone, USP is practically insoluble in water, slightly soluble in ethanol (96 per cent) and in methylene chloride. Prednisone delayed-release tablet is a delayed-release prednisone tablet. It consists of a prednisone-containing core tablet in an inactive shell, which delays the onset of in vitro drug dissolution by approximately 4 hours. Each tablet contains 1 mg, or 2 mg of prednisone, USP with the following inactive ingredients: dibasic calcium phosphate dihydrate, colloidal silicon dioxide, croscarmellose sodium, glycerol dibehenate, lactose monohydrate, magnesium stearate, povidone, yellow ferric oxide and red ferric oxide. Each prednisone delayed-release tablet contains 30 mg of phosphorous. Each prednisone delayed-release tablet contains less than 5 mg of sodium.</Description>
  </NDC>
  <NDC>
    <NDCCode>76296-010-40</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (76296-010-40)  &gt; 40 mL in 1 BOTTLE</PackageDescription>
    <NDC11Code>76296-0010-40</NDC11Code>
    <ProductNDC>76296-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Vinoperfect Broad Spectrum Spf 15 Day Perfecting Fluid</ProprietaryName>
    <NonProprietaryName>Avobenzone, Octinoxate, Octisalate, Octocrylene</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20140306</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Caudalie USA Inc.</LabelerName>
    <SubstanceName>AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE</SubstanceName>
    <StrengthNumber>30; 39.96; 50; 80</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL; mg/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2016-12-06</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>85951-010-01</NDCCode>
    <PackageDescription>1 g in 1 TUBE (85951-010-01) </PackageDescription>
    <NDC11Code>85951-0010-01</NDC11Code>
    <ProductNDC>85951-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Eczema Therapy</ProprietaryName>
    <NonProprietaryName>Colloidal Oatmeal</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20250806</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M016</ApplicationNumber>
    <LabelerName>SilverCeuticals</LabelerName>
    <SubstanceName>OATMEAL</SubstanceName>
    <StrengthNumber>.96</StrengthNumber>
    <StrengthUnit>g/96g</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-05-15</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250806</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Directions: 1 Clean the affected area, 2 Apply a small amount of this product on the area once daily, 3 May be covered with a sterile bandage, 4 If bandaged, let dry first.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>85951-010-34</NDCCode>
    <PackageDescription>1 g in 1 BOTTLE, DISPENSING (85951-010-34) </PackageDescription>
    <NDC11Code>85951-0010-34</NDC11Code>
    <ProductNDC>85951-010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Eczema Therapy</ProprietaryName>
    <NonProprietaryName>Colloidal Oatmeal</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20250806</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M016</ApplicationNumber>
    <LabelerName>SilverCeuticals</LabelerName>
    <SubstanceName>OATMEAL</SubstanceName>
    <StrengthNumber>.96</StrengthNumber>
    <StrengthUnit>g/96g</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-05-15</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250806</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Directions: 1 Clean the affected area, 2 Apply a small amount of this product on the area once daily, 3 May be covered with a sterile bandage, 4 If bandaged, let dry first.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>99207-010-10</NDCCode>
    <PackageDescription>1 BOTTLE, PLASTIC in 1 CARTON (99207-010-10)  &gt; 120 mL in 1 BOTTLE, PLASTIC</PackageDescription>
    <NDC11Code>99207-0010-10</NDC11Code>
    <ProductNDC>99207-010</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Loprox</ProprietaryName>
    <NonProprietaryName>Ciclopirox</NonProprietaryName>
    <DosageFormName>SHAMPOO</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20030320</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA021159</ApplicationNumber>
    <LabelerName>Bausch Health US, LLC</LabelerName>
    <SubstanceName>CICLOPIROX</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/.96mL</StrengthUnit>
    <Pharm_Classes>Decreased DNA Replication [PE], Decreased Protein Synthesis [PE], Decreased RNA Replication [PE], Protein Synthesis Inhibitors [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20030320</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>LOPROX® (ciclopirox) Shampoo, 1% is indicated for the topical treatment of seborrheic dermatitis of the scalp in adults.</IndicationAndUsage>
    <Description>LOPROX (ciclopirox) Shampoo, 1% contains the synthetic antifungal agent ciclopirox for topical use. Each gram (equivalent to 0.96 mL) of LOPROX Shampoo contains 10 mg ciclopirox in a shampoo base consisting of disodium laureth sulfosuccinate, laureth-2, purified water, sodium chloride, and sodium laureth sulfate. LOPROX Shampoo is a colorless, translucent solution. The chemical name for ciclopirox is 6-cyclohexyl-1-hydroxy-4-methyl-2(1H)-pyridone, with the empirical formula C12H17NO2 and a molecular weight of 207.27. The CAS Registry Number is [29342-05-0]. The chemical structure is.</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>
</NDCList>
                    

<NDCList><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>27281-001-96</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>27281-008-96</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>27281-009-96</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>27281-011-96</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>11084-010-96</NDCCode><ProprietaryName>Refresh Antibac Foam</ProprietaryName><NonProprietaryName>Benzalkonium Chloride</NonProprietaryName></NDC><NDC><NDCCode>25373-010-07</NDCCode><ProprietaryName>Helium</ProprietaryName><NonProprietaryName>Helium</NonProprietaryName></NDC><NDC><NDCCode>50425-010-96</NDCCode><ProprietaryName>Scrub Care Povidone Iodine Cleansing Scrub</ProprietaryName><NonProprietaryName>Povidone Iodine</NonProprietaryName></NDC><NDC><NDCCode>58406-010-96</NDCCode><ProprietaryName>Enbrel</ProprietaryName><NonProprietaryName>Etanercept</NonProprietaryName></NDC><NDC><NDCCode>63323-010-96</NDCCode><ProprietaryName>Gentamicin</ProprietaryName><NonProprietaryName>Gentamicin Sulfate</NonProprietaryName></NDC><NDC><NDCCode>67777-010-03</NDCCode><ProprietaryName>Sannytize Hand Sanitizer</ProprietaryName><NonProprietaryName>Hand Sanitizer</NonProprietaryName></NDC><NDC><NDCCode>72683-010-01</NDCCode><ProprietaryName>Roll Pain Away Lavender</ProprietaryName><NonProprietaryName>Capsaicin</NonProprietaryName></NDC><NDC><NDCCode>73143-010-03</NDCCode><ProprietaryName>Menthol</ProprietaryName><NonProprietaryName>Menthol</NonProprietaryName></NDC><NDC><NDCCode>80808-010-86</NDCCode><ProprietaryName>Hygenize Alcohol Wipes</ProprietaryName><NonProprietaryName>Alcohol</NonProprietaryName></NDC><NDC><NDCCode>83176-010-01</NDCCode><ProprietaryName>Oheal Manuka Honey Eczema Cream</ProprietaryName><NonProprietaryName>Manuka Honey Eczema Cream</NonProprietaryName></NDC><NDC><NDCCode>10631-010-30</NDCCode><ProprietaryName>Kapspargo</ProprietaryName><NonProprietaryName>Metoprolol Succinate</NonProprietaryName></NDC><NDC><NDCCode>63304-010-30</NDCCode><ProprietaryName>Metoprolol Succinate</ProprietaryName><NonProprietaryName>Metoprolol Succinate</NonProprietaryName></NDC><NDC><NDCCode>71597-010-02</NDCCode><ProprietaryName>Acwell Sensitive Solu Tion Sun Control</ProprietaryName><NonProprietaryName>Zinc Oxide, Titanium Dioxide</NonProprietaryName></NDC><NDC><NDCCode>74157-010-30</NDCCode><ProprietaryName>Prednisone Delayed Release</ProprietaryName><NonProprietaryName>Prednisone</NonProprietaryName></NDC><NDC><NDCCode>76296-010-40</NDCCode><ProprietaryName>Vinoperfect Broad Spectrum Spf 15 Day Perfecting Fluid</ProprietaryName><NonProprietaryName>Avobenzone, Octinoxate, Octisalate, Octocrylene</NonProprietaryName></NDC><NDC><NDCCode>85951-010-01</NDCCode><ProprietaryName>Eczema Therapy</ProprietaryName><NonProprietaryName>Colloidal Oatmeal</NonProprietaryName></NDC><NDC><NDCCode>85951-010-34</NDCCode><ProprietaryName>Eczema Therapy</ProprietaryName><NonProprietaryName>Colloidal Oatmeal</NonProprietaryName></NDC><NDC><NDCCode>99207-010-10</NDCCode><ProprietaryName>Loprox</ProprietaryName><NonProprietaryName>Ciclopirox</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></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",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-3574",
      "MailingAddressFaxNumber": "425-881-0230",
      "FirstLinePracticeLocationAddress": "16150 NE 85TH ST STE 206",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3543",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-3574",
      "PracticeLocationAddressFaxNumber": "425-881-0230",
      "EnumerationDate": "11/07/2006",
      "LastUpdateDate": "07/08/2007",
      "AuthorizedOfficialLastName": "OTTEN",
      "AuthorizedOfficialFirstName": "LARRY",
      "AuthorizedOfficialMiddleName": "C",
      "AuthorizedOfficialTitle": "DR",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "O.D.",
      "AuthorizedOfficialTelephoneNumber": "425-885-3574",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "OD00001172",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y",
      "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."
    },
    {
      "NPI": "1376755009",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "PERIMAN",
      "FirstName": "LAURA",
      "MiddleName": "MARIE",
      "NamePrefix": "DR.",
      "Credential": "MD",
      "FirstLineMailingAddress": "623 W HIGHLAND DR",
      "MailingAddressCityName": "SEATTLE",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98119-3446",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "206-282-2716",
      "FirstLinePracticeLocationAddress": "16150 NE 85TH ST STE 206",
      "SecondLinePracticeLocationAddress": "REDMOND EYE CLINIC",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3543",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-3574",
      "EnumerationDate": "05/04/2007",
      "LastUpdateDate": "07/08/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207W00000X",
      "Taxonomy1": "Ophthalmology",
      "LicenseNumber1": "MD00039796",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1659320539",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "MONTECILLO",
      "FirstName": "RANIA",
      "MiddleName": "B",
      "NamePrefix": "DR.",
      "Credential": "OD",
      "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": "05/09/2006",
      "LastUpdateDate": "12/19/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "3680",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1427560267",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "ABOU SHADI",
      "FirstName": "RANIA",
      "NamePrefix": "MRS.",
      "Credential": "RPH",
      "FirstLineMailingAddress": "8862 161ST AVENUE NE",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-883-9532",
      "MailingAddressFaxNumber": "425-882-2743",
      "FirstLinePracticeLocationAddress": "8862 161ST AVENUE NE",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-883-9532",
      "PracticeLocationAddressFaxNumber": "425-882-2743",
      "EnumerationDate": "11/02/2017",
      "LastUpdateDate": "11/02/2017",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "3336C0003X",
      "Taxonomy1": "Community/Retail Pharmacy",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1528050523",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "DESCHUTES EYE CLINIC PC",
      "OtherOrgName": "THE EYE SURGERY INSTITUTE",
      "OtherOrgNameTypeCode": "3",
      "FirstLineMailingAddress": "813 SW HIGHLAND AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-3123",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-548-7170",
      "MailingAddressFaxNumber": "541-548-3842",
      "FirstLinePracticeLocationAddress": "813 SW HIGHLAND AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-3123",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-548-7170",
      "PracticeLocationAddressFaxNumber": "541-548-3842",
      "EnumerationDate": "08/17/2005",
      "LastUpdateDate": "12/01/2010",
      "AuthorizedOfficialLastName": "TRAUSTASON",
      "AuthorizedOfficialFirstName": "OLI",
      "AuthorizedOfficialMiddleName": "I",
      "AuthorizedOfficialTitle": "PRESIDENT",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "M.D.",
      "AuthorizedOfficialTelephoneNumber": "541-548-7170",
      "TaxonomyCode1": "207W00000X",
      "Taxonomy1": "Ophthalmology",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "053857000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierState1": "OR",
      "OtherIdentifierIssuer1": "REGENCE BCBS",
      "OtherIdentifier2": "CJ8770",
      "OtherIdentifierType2": "OTHER",
      "OtherIdentifierState2": "OR",
      "OtherIdentifierIssuer2": "RAILROAD MEDICARE",
      "OtherIdentifier3": "38080A",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierState3": "OR",
      "OtherIdentifierIssuer3": "CLEAR CHOICE",
      "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": "1477596252",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "EYE CARE SPECIALISTS NORTHWEST PLLC",
      "OtherOrgName": "THE CHILDRENS EYE DOCTORS, THE FAMILY EYE DOCTORS, WOODLAWN OPTICAL",
      "OtherOrgNameTypeCode": "3",
      "FirstLineMailingAddress": "17130 AVONDALE WAY NE",
      "SecondLineMailingAddress": "SUITE 111",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-6600",
      "MailingAddressFaxNumber": "425-885-6580",
      "FirstLinePracticeLocationAddress": "17130 AVONDALE WAY NE",
      "SecondLinePracticeLocationAddress": "SUITE 111",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-6600",
      "PracticeLocationAddressFaxNumber": "425-885-6580",
      "EnumerationDate": "06/13/2006",
      "LastUpdateDate": "03/03/2008",
      "AuthorizedOfficialLastName": "LENART",
      "AuthorizedOfficialFirstName": "THOMAS",
      "AuthorizedOfficialTitle": "OWNER",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "MD PHD",
      "AuthorizedOfficialTelephoneNumber": "425-885-6600",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "156FX1800X",
      "Taxonomy2": "Optician",
      "PrimaryTaxonomySwitch2": "N",
      "TaxonomyCode3": "207W00000X",
      "Taxonomy3": "Ophthalmology",
      "PrimaryTaxonomySwitch3": "Y",
      "OtherIdentifier1": "1568514032",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "NPI",
      "OtherIdentifier2": "1740297829",
      "OtherIdentifierType2": "OTHER",
      "OtherIdentifierIssuer2": "NPI",
      "OtherIdentifier3": "1205989522",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "NPI",
      "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.",
      "HealthcareProviderTaxonomyGroup2": "193200000X MULTI-SPECIALTY GROUP",
      "HealthcareProviderTaxonomyGroupDescription2": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization.",
      "HealthcareProviderTaxonomyGroup3": "193200000X MULTI-SPECIALTY GROUP",
      "HealthcareProviderTaxonomyGroupDescription3": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization."
    },
    {
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    {
      "NPI": "1629068499",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "FAHOURY",
      "FirstName": "RANIA",
      "NamePrefix": "DR.",
      "Credential": "MD",
      "FirstLineMailingAddress": "4411 N HOLLAND SYLVANIA RD",
      "SecondLineMailingAddress": "SUITE 201",
      "MailingAddressCityName": "TOLEDO",
      "MailingAddressStateName": "OH",
      "MailingAddressPostalCode": "43623-3525",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "419-843-3627",
      "MailingAddressFaxNumber": "419-843-9697",
      "FirstLinePracticeLocationAddress": "4411 N HOLLAND SYLVANIA RD",
      "SecondLinePracticeLocationAddress": "SUITE 201",
      "PracticeLocationAddressCityName": "TOLEDO",
      "PracticeLocationAddressStateName": "OH",
      "PracticeLocationAddressPostalCode": "43623-3525",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "419-843-3627",
      "PracticeLocationAddressFaxNumber": "419-843-9697",
      "EnumerationDate": "10/24/2005",
      "LastUpdateDate": "09/02/2011",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "35086663",
      "LicenseNumberStateCode1": "OH",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "2621621",
      "OtherIdentifierType1": "MEDICAID",
      "OtherIdentifierState1": "OH",
      "OtherIdentifier2": "P00401238",
      "OtherIdentifierType2": "OTHER",
      "OtherIdentifierState2": "OH",
      "OtherIdentifierIssuer2": "RAILROAD MEDICARE"
    },
    {
      "NPI": "1033186986",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "NICOLA",
      "FirstName": "RANIA",
      "MiddleName": "SOLIMAN",
      "NamePrefix": "DR.",
      "Credential": "DDS",
      "FirstLineMailingAddress": "110 S WOODLAND ST",
      "MailingAddressCityName": "WINTER GARDEN",
      "MailingAddressStateName": "FL",
      "MailingAddressPostalCode": "34787-3546",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "407-905-8827",
      "MailingAddressFaxNumber": "407-645-4587",
      "FirstLinePracticeLocationAddress": "7900 FOREST CITY RD",
      "PracticeLocationAddressCityName": "ORLANDO",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "32810-3002",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "407-905-8827",
      "PracticeLocationAddressFaxNumber": "407-645-4587",
      "EnumerationDate": "02/28/2006",
      "LastUpdateDate": "07/28/2017",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "1223G0001X",
      "Taxonomy1": "General Practice",
      "LicenseNumber1": "DN15582",
      "LicenseNumberStateCode1": "FL",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "122300000X",
      "Taxonomy2": "Dentist",
      "LicenseNumber2": "DN15582",
      "LicenseNumberStateCode2": "FL",
      "PrimaryTaxonomySwitch2": "Y",
      "OtherIdentifier1": "075156100",
      "OtherIdentifierType1": "MEDICAID",
      "OtherIdentifierState1": "FL"
    },
    {
      "NPI": "1720032899",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ALBATAINEH",
      "FirstName": "RANIA",
      "MiddleName": "QASSIEM",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "11476 OKEECHOBEE BLVD",
      "MailingAddressCityName": "ROYAL PALM BEACH",
      "MailingAddressStateName": "FL",
      "MailingAddressPostalCode": "33411-8715",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "561-204-5111",
      "MailingAddressFaxNumber": "561-204-5150",
      "FirstLinePracticeLocationAddress": "11476 OKEECHOBEE BLVD",
      "PracticeLocationAddressCityName": "ROYAL PALM BEACH",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "33411-8715",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "561-204-5111",
      "PracticeLocationAddressFaxNumber": "561-204-5150",
      "EnumerationDate": "05/21/2006",
      "LastUpdateDate": "09/11/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "ME 79876",
      "LicenseNumberStateCode1": "FL",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1326095100",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ROSBOROUGH",
      "FirstName": "RANIA",
      "MiddleName": "BAJWA",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "3100 WYMAN PARK DR",
      "MailingAddressCityName": "BALTIMORE",
      "MailingAddressStateName": "MD",
      "MailingAddressPostalCode": "21211-2803",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "410-338-3500",
      "FirstLinePracticeLocationAddress": "3601 SW 160TH AVE",
      "SecondLinePracticeLocationAddress": "SUITE 250",
      "PracticeLocationAddressCityName": "MIRAMAR",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "33027-6308",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "877-866-7123",
      "EnumerationDate": "05/27/2006",
      "LastUpdateDate": "12/10/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "D0063732",
      "LicenseNumberStateCode1": "MD",
      "PrimaryTaxonomySwitch1": "Y",
      "TaxonomyCode2": "207Q00000X",
      "Taxonomy2": "Family Medicine",
      "LicenseNumber2": "0101257197",
      "LicenseNumberStateCode2": "VA",
      "PrimaryTaxonomySwitch2": "N"
    },
    {
      "NPI": "1528015310",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "HUSSEINI",
      "FirstName": "RANIA",
      "MiddleName": "I",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "111 CYPRESS ST",
      "MailingAddressCityName": "BROOKLINE",
      "MailingAddressStateName": "MA",
      "MailingAddressPostalCode": "02445-6002",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "508-718-4050",
      "FirstLinePracticeLocationAddress": "20 PATRIOT PL",
      "PracticeLocationAddressCityName": "FOXBORO",
      "PracticeLocationAddressStateName": "MA",
      "PracticeLocationAddressPostalCode": "02035-1375",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "508-718-4050",
      "EnumerationDate": "05/27/2006",
      "LastUpdateDate": "04/17/2012",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "209649",
      "LicenseNumberStateCode1": "MA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1760429591",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "RAYES-DANAN",
      "FirstName": "RANIA",
      "NamePrefix": "DR.",
      "Credential": "MD",
      "OtherLastName": "RAYES",
      "OtherFirstName": "RANIA",
      "OtherLastNameTypeCode": "1",
      "FirstLineMailingAddress": "2500 METROHEALTH DR",
      "MailingAddressCityName": "CLEVELAND",
      "MailingAddressStateName": "OH",
      "MailingAddressPostalCode": "44109-1900",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "216-778-7800",
      "FirstLinePracticeLocationAddress": "2500 METROHEALTH DR",
      "PracticeLocationAddressCityName": "CLEVELAND",
      "PracticeLocationAddressStateName": "OH",
      "PracticeLocationAddressPostalCode": "44109-1900",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "216-778-7800",
      "EnumerationDate": "06/01/2006",
      "LastUpdateDate": "01/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207ZP0102X",
      "Taxonomy1": "Anatomic Pathology & Clinical Pathology",
      "LicenseNumber1": "35086346",
      "LicenseNumberStateCode1": "OH",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "2687703",
      "OtherIdentifierType1": "MEDICAID",
      "OtherIdentifierState1": "OH"
    },
    {
      "NPI": "1699717660",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "AMPEY",
      "FirstName": "RANIA",
      "MiddleName": "L",
      "Credential": "LPC",
      "FirstLineMailingAddress": "5930 LOVERS LN",
      "SecondLineMailingAddress": "PREMIER NEUROPSYCHIATRY, PLC",
      "MailingAddressCityName": "PORTAGE",
      "MailingAddressStateName": "MI",
      "MailingAddressPostalCode": "49002-1673",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "269-873-1611",
      "FirstLinePracticeLocationAddress": "5930 LOVERS LN",
      "SecondLinePracticeLocationAddress": "PREMIER NEUROPSYCHIATRY, PLC",
      "PracticeLocationAddressCityName": "PORTAGE",
      "PracticeLocationAddressStateName": "MI",
      "PracticeLocationAddressPostalCode": "49002-1673",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "269-873-1611",
      "EnumerationDate": "06/12/2006",
      "LastUpdateDate": "12/30/2010",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional",
      "LicenseNumber1": "6401007658",
      "LicenseNumberStateCode1": "MI",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1801839667",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ABOUJAOUDE",
      "FirstName": "RANIA",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "PO BOX 1283",
      "MailingAddressCityName": "MEDFORD",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08055-6283",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "609-677-1046",
      "MailingAddressFaxNumber": "609-677-1306",
      "FirstLinePracticeLocationAddress": "200 TRENTON RD",
      "PracticeLocationAddressCityName": "BROWNS MILLS",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08015-1705",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "609-677-1046",
      "PracticeLocationAddressFaxNumber": "609-677-1306",
      "EnumerationDate": "06/13/2006",
      "LastUpdateDate": "09/15/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207RI0200X",
      "Taxonomy1": "Infectious Disease",
      "LicenseNumber1": "39215",
      "LicenseNumberStateCode1": "KY",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "207RI0200X",
      "Taxonomy2": "Infectious Disease",
      "LicenseNumber2": "25MA07672000",
      "LicenseNumberStateCode2": "NJ",
      "PrimaryTaxonomySwitch2": "Y"
    },
    {
      "NPI": "1184645301",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "BAIK",
      "FirstName": "RANIA",
      "Credential": "D.O.",
      "FirstLineMailingAddress": "602 ROUTE 169",
      "SecondLineMailingAddress": "PO BOX 865",
      "MailingAddressCityName": "WOODSTOCK",
      "MailingAddressStateName": "CT",
      "MailingAddressPostalCode": "06281-2225",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "860-821-3406",
      "MailingAddressFaxNumber": "860-821-3407",
      "FirstLinePracticeLocationAddress": "602 ROUTE 169",
      "PracticeLocationAddressCityName": "WOODSTOCK",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06281-2225",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "860-821-3406",
      "PracticeLocationAddressFaxNumber": "860-821-3407",
      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "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",
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}
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