RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (38 ms elapsed)

{
  "NDC": [
    {
      "NDCCode": "61626-0104-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0104-4) ",
      "NDC11Code": "61626-0104-04",
      "ProductNDC": "61626-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Water",
      "NonProprietaryName": "Aconitum Nap, Arsenicum Alb, Borax, Calc Phos, Gelsenium, Lycopodium, Phosphoricum Ac, Picricum Ac, Plumb Met, Solidago",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ACONITUM NAPELLUS; ARSENIC TRIOXIDE; SODIUM BORATE; TRIBASIC CALCIUM PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; PICRIC ACID; LEAD; SOLIDAGO VIRGAUREA FLOWERING TOP",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of fear, weak - paralyzed will, dread, and related emotions. Sensory, spinal and extremity disorders. Ear - earache, bone - occipital and neck pain, weak spine and lower extremity disorders.**."
    },
    {
      "NDCCode": "61626-0098-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0098-4) ",
      "NDC11Code": "61626-0098-04",
      "ProductNDC": "61626-0098",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Flu Immune",
      "NonProprietaryName": "Anas Barbarie Hepatis Et Cordis Extractum",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE",
      "StrengthNumber": "200",
      "StrengthUnit": "[hp_C]/59mL",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of flu-related symptoms such as aches, pains, fever and chills. Flu Immune can be used at the onset of flu-like symptoms and as preventative. Flu Immune helps stimulate the body's immunity and is reccommended as first line of defense against flu-like symptoms. **."
    },
    {
      "NDCCode": "61626-0099-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0099-4) ",
      "NDC11Code": "61626-0099-04",
      "ProductNDC": "61626-0099",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Pain Relief",
      "NonProprietaryName": "Arnica, Chamomilla, Hypericum, Ignatia, Symphytum",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ARNICA MONTANA; MATRICARIA CHAMOMILLA; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; COMFREY ROOT",
      "StrengthNumber": "12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of general pain, includingm symptoms related to joints, bones, muscles, minor bruises, spinal pain and pain due to arthiritis. **."
    },
    {
      "NDCCode": "61626-0100-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0100-4) ",
      "NDC11Code": "61626-0100-04",
      "ProductNDC": "61626-0100",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Day And Night Vitals",
      "NonProprietaryName": "Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "GARLIC; ALOE VERA LEAF; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; TRIBASIC CALCIUM PHOSPHATE; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; CHOLESTEROL; CLEMATIS RECTA FLOWERING TOP; MARSDENIA CONDURANGO BARK; GAMBOGE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; POTASSIUM BROMIDE; DIBASIC POTASSIUM PHOSPHATE; LYCOPODIUM CLAVATUM SPORE; SODIUM CARBONATE; PASSIFLORA INCARNATA TOP; SENNA LEAF; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SPIGELIA ANTHELMIA; SPONGIA OFFICINALIS SKELETON, ROASTED; VERATRUM VIRIDE ROOT",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of symptoms related to low vitality and function of the Large intestine, Stomach, Spleen, Heart, Small Intestine, Bladder, Kidney, Sex Organs, Thyroid, Adrenal, Gall Bladder, Liver and Lung.**."
    },
    {
      "NDCCode": "61626-0101-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0101-4) ",
      "NDC11Code": "61626-0101-04",
      "ProductNDC": "61626-0101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Yin-yang Balance",
      "NonProprietaryName": "Adamas, Agaricus Musc, Agnus, Aletris, Angelica Sin, Arg Nit, Arnica, Avena, Baryta, Graphites, Kali Brom, Kreosotum, Lycopodium, Ocimum Sanc, Phosphoricum Ac, Selenium, Sepia, Thuja Occ.",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "DIAMOND; AMANITA MUSCARIA FRUITING BODY; CHASTE TREE; ALETRIS FARINOSA ROOT; ANGELICA SINENSIS ROOT; SILVER NITRATE; ARNICA MONTANA; AVENA SATIVA FLOWERING TOP; BARIUM IODIDE; GRAPHITE; POTASSIUM BROMIDE; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; OCIMUM TENUIFLORUM TOP; PHOSPHORIC ACID; SELENIUM; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of hormonal disbalance in men and women.**."
    },
    {
      "NDCCode": "61626-0102-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0102-4) ",
      "NDC11Code": "61626-0102-04",
      "ProductNDC": "61626-0102",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Earth",
      "NonProprietaryName": "Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus.",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "GOLD; SILVER NITRATE; CAUSTICUM; CINCHONA OFFICINALIS BARK; MARSDENIA CONDURANGO BARK; CEANOTHUS AMERICANUS LEAF; EUPHRASIA STRICTA; FUCUS VESICULOSUS; GALLIC ACID MONOHYDRATE; IRIS VERSICOLOR ROOT; SODIUM CARBONATE; NITRIC ACID; PHOSPHORUS",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE. For the temporary relief of the neuro-emotional (automatic nervous system - non psychiatric) disorders of oversympathy, low self esteem and related emotions. Sensory, spinal and extremity disorders. Relief of symptoms of colds, sinus problems. Digestive, mouth saliva, taste disorders. Weak spine and lower extremity disorders.**​."
    },
    {
      "NDCCode": "61626-0103-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0103-4) ",
      "NDC11Code": "61626-0103-04",
      "ProductNDC": "61626-0103",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Metal",
      "NonProprietaryName": "Aluminia, Ammon Carb, Anacardium, Antimon Crud, Hydrastis, Ignatia, Mag Phos, Nat Mur, Nitricum Ac, Osmium, Paraffinum, Senna, Silicea, Spongia",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ALUMINUM OXIDE; AMMONIUM CARBONATE; ANACARDIUM OCCIDENTALE FRUIT; ANTIMONY TRISULFIDE; GOLDENSEAL; STRYCHNOS IGNATII SEED; MAGNESIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; NITRIC ACID; OSMIUM; PARAFFIN; SENNA LEAF; SILICON DIOXIDE; SPONGIA OFFICINALIS SKELETON, ROASTED",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE. For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of grief, dogmatically positioned, sadness, crying, and related emotions. Sensory, spinal and extremity disorders. Nose - smell, mucous. Constipation. Skin - dry, itching. Weak spine disorders.**."
    },
    {
      "NDCCode": "61626-0105-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0105-4) ",
      "NDC11Code": "61626-0105-04",
      "ProductNDC": "61626-0105",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Wood",
      "NonProprietaryName": "Belladonna, Berber Vulg, Carduus Mar, Chelidonium Maj, Cholesterinum, Colocynthis, Kali Carb, Nat Phos, Nitricum Ac, Nux Vom, Platinum Met, Sepia",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ATROPA BELLADONNA; BERBERIS VULGARIS ROOT BARK; MILK THISTLE; CHELIDONIUM MAJUS; CHOLESTEROL; CITRULLUS COLOCYNTHIS FRUIT PULP; POTASSIUM CARBONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PLATINUM; SEPIA OFFICINALIS JUICE",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non phychiatric) disorders of anger, resentment and related emotions. Temporary relief of headache symptoms. Billousness, eye - minor eye irritation, tears, muscle, neck, weak spine and lower extremity disorders.**."
    },
    {
      "NDCCode": "61626-0106-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0106-4) ",
      "NDC11Code": "61626-0106-04",
      "ProductNDC": "61626-0106",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Fire",
      "NonProprietaryName": "Apil Mel, Baptisia, Baryta Carb, Hamamelis, Kali Brom, Kali Phos, Lachesis, Lilium, Petroleum, Phosphoricum Ac, Spigelia Anth, Sulphur, Veratrum Vir",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; POTASSIUM BROMIDE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; LILIUM LANCIFOLIUM BULB; KEROSENE; PHOSPHORIC ACID; SPIGELIA ANTHELMIA; SULFUR; VERATRUM VIRIDE ROOT",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]",
      "Status": "Active",
      "LastUpdate": "2021-01-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of vulnerability, lost, and related emotions. Minor circulation irregularities, fatigue. Tongue, perspiration, spine, and upper extremity disorders. Temporary relief of chest congestion and minor pain in reproductive organs.**."
    },
    {
      "NDCCode": "61626-0107-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0107-4) ",
      "NDC11Code": "61626-0107-04",
      "ProductNDC": "61626-0107",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Para Solve",
      "NonProprietaryName": "Calc Carb, Chenopodium Anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc Corros, Nat Phos, Santoninum, Senna, Spigelia Anth, Stannum Met, Tanacetum, Teuricum Mar, Zingiber",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "OYSTER SHELL CALCIUM CARBONATE, CRUDE; DYSPHANIA AMBROSIOIDES; ARTEMISIA CINA PRE-FLOWERING TOP; CROTON TIGLIUM SEED; DRYOPTERIS FILIX-MAS ROOT; GAMBOGE; PUNICA GRANATUM ROOT BARK; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SANTONIN; SENNA LEAF; SPIGELIA ANTHELMIA; TIN; TANACETUM VULGARE TOP; TEUCRIUM MARUM; GINGER",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL",
      "Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE​: For the temporary relief of gastrointestinal symptoms such as gas, bloating, stomach upset, abdominal discomfort which may be accompanied  by pale face or circles under the eyes, bad breath, bariable appetite, localized ithching, postnasal drip, canker sores. irritability, back pain, resltess sleep, and sensitivity in lower right abdominal area. Temporary relief of cough.**."
    },
    {
      "NDCCode": "61626-0108-4",
      "PackageDescription": "59.1 mL in 1 BOTTLE (61626-0108-4) ",
      "NDC11Code": "61626-0108-04",
      "ProductNDC": "61626-0108",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Flora Plus",
      "NonProprietaryName": "Aloe, Alumina, Antimon Crud, Arg Nit, Chelidonium Maj, Gambogia, Graphites, Hydrastis, Lycopodium, Silicea",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ALOE VERA LEAF; ALUMINUM OXIDE; ANTIMONY TRISULFIDE; SILVER NITRATE; CHELIDONIUM MAJUS; GAMBOGE; GRAPHITE; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; SILICON DIOXIDE",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For temporary relief of bowel congestions-constipation, gas, bloating  Digestive disturbance and intestinal complaints from bread, acids, sour wines, fermentable foods-sweets-yeast  ​​ White or yellow film on tongue  ​ Relief of symptoms associated with yeast infections  Sensitivity in lower right abdominal area. **."
    },
    {
      "NDCCode": "61626-0109-4",
      "PackageDescription": "59.1 mL in 1 BOTTLE (61626-0109-4) ",
      "NDC11Code": "61626-0109-04",
      "ProductNDC": "61626-0109",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Allergy",
      "NonProprietaryName": "Allium Sat, Anacardium, Apis Mel, Gambogia, Merc Solub, Nat Carb, Nitricum Ac, Nux Vom, Phosphorus, Pulsatilla, Sulphur",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Net Remedies",
      "SubstanceName": "GARLIC; ANACARDIUM OCCIDENTALE FRUIT; APIS MELLIFERA; GAMBOGE; MERCURIUS SOLUBILIS; SODIUM CARBONATE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; ANEMONE PULSATILLA; SULFUR",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL",
      "Pharm_Classes": "Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: For the temporary relief of allergic reactions from environmental agents, slight errors in diet or certain foods causing symptoms of sensitivity, mood changes, headaches, tiredness, sinus congestion, itchy or burning eyes, dyspepsia, bloating, gas, sensitivity in lower right abdominal area.**."
    },
    {
      "NDCCode": "61626-0110-4",
      "PackageDescription": "59.1 mL in 1 BOTTLE (61626-0110-4) ",
      "NDC11Code": "61626-0110-04",
      "ProductNDC": "61626-0110",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Er 911",
      "NonProprietaryName": "Aconitum Nap, Apis Mel, Arnica, Arsenicum Alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus Canadensis, Clematis Erecta, Ferrum Phos, Histaminum, Hypericum, Ignatia, Impatiens Glan Flos, Ornithogalum, Passiflora, Phosphorus, Prunus Cerasifera, Rhus Tox, Sulphur, Symphytum, Vertarum Alb",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Net Remedies",
      "SubstanceName": "ACONITUM NAPELLUS; APIS MELLIFERA; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA CHAMOMILLA; HELIANTHEMUM CANADENSE; CLEMATIS RECTA FLOWERING TOP; FERROSOFERRIC PHOSPHATE; HISTAMINE DIHYDROCHLORIDE; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; IMPATIENS GLANDULIFERA FLOWER; ORNITHOGALUM UMBELLATUM; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; PRUNUS CERASIFERA FLOWER; TOXICODENDRON PUBESCENS LEAF; SULFUR; COMFREY ROOT; VERATRUM ALBUM ROOT",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL",
      "Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: For the temporary relief of emotional, mental, or physical trauma, high pressure or stressful situations  Symptomatic relief of nervous tension, stress, dread and fever. Temporary relief of cold and flu-like symptoms. Overexertion ​​ Strains  Tearfulness  Fearfulness  Oversensitivity  Minor nerve pain and burning  ​ Quieting effect on nervous system.**."
    },
    {
      "NDCCode": "61626-0111-4",
      "PackageDescription": "59.1 mL in 1 BOTTLE (61626-0111-4) ",
      "NDC11Code": "61626-0111-04",
      "ProductNDC": "61626-0111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Scars-adhesions",
      "NonProprietaryName": "Calc Fluor, Causticum, Graphites, Hydrofluoricum Ac, Lachesis, Plumb Met, Rhus Tox, Sepia, Silicea, Thiosinaminum",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "CALCIUM FLUORIDE; CAUSTICUM; GRAPHITE; HYDROFLUORIC ACID; LACHESIS MUTA VENOM; LEAD; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; ALLYLTHIOUREA",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​Helps absorption of scars-fibrous tissue adhesions  For the temporary relief of itching of scars  Feelins of spasm pressure and tightness sensation in internal organs, esophagus and stomach  ​​ Colic type symptoms.**."
    },
    {
      "NDCCode": "61626-0112-4",
      "PackageDescription": "59 mL in 1 BOTTLE (61626-0112-4) ",
      "NDC11Code": "61626-0112-04",
      "ProductNDC": "61626-0112",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Visceral Polarity",
      "NonProprietaryName": "Aconitum Nap, Arg Nit, Chininum Pur, Echinacea Purp, Plum Met, Sepia, Sulphuricum Ac",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20181204",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "NET Remedies",
      "SubstanceName": "ACONITUM NAPELLUS; SILVER NITRATE; QUININE; ECHINACEA PURPUREA; FERRIC FERROCYANIDE; GELSEMIUM SEMPERVIRENS ROOT; HOPS; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; LEAD; SEPIA OFFICINALIS JUICE; SULFURIC ACID",
      "StrengthNumber": "12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12",
      "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
      "Pharm_Classes": "Allergens [CS], Allergens [CS], Antimalarial [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Chelating Activity [MoA], Decorporation Agent [EPC], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2021-01-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20181204",
      "SamplePackage": "N",
      "IndicationAndUsage": "​INDICATIONS FOR USE: ​For the temporary relief of lack of general emotional, physical, or mental balance  Minor nervous system tension, confusion, nervousness, fatigue  ​​ Feelings of spasm pressure and tightness sensation in internal organs, esophagus and stomach  Temporary relief of heartburn ​ General tone of nervous and digestive systems.**."
    },
    {
      "NDCCode": "11523-0104-4",
      "PackageDescription": "4 BLISTER PACK in 1 CARTON (11523-0104-4)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK",
      "NDC11Code": "11523-0104-04",
      "ProductNDC": "11523-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Claritin",
      "NonProprietaryName": "Loratadine",
      "DosageFormName": "TABLET, CHEWABLE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20230205",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA210033",
      "LabelerName": "Bayer HealthCare LLC.",
      "SubstanceName": "LORATADINE",
      "StrengthNumber": "5",
      "StrengthUnit": "mg/1",
      "Status": "Active",
      "LastUpdate": "2025-12-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230208",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: 1 runny nose, 2 sneezing, 3 itchy, watery eyes, 4 itching of the nose or throat."
    },
    {
      "NDCCode": "13630-0104-4",
      "PackageDescription": "177 mL in 1 CAN (13630-0104-4) ",
      "NDC11Code": "13630-0104-04",
      "ProductNDC": "13630-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Miami Beach",
      "ProprietaryNameSuffix": "Spf 50 Kids C/s Sunscreen",
      "NonProprietaryName": "Avobenzone, Homosalate, Octisalate, And Octocrylene",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20160229",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Prime Packaging Inc.",
      "SubstanceName": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
      "StrengthNumber": "30.66; 102.2; 51.1; 28.11",
      "StrengthUnit": "mg/mL; mg/mL; mg/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2023-01-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20221231",
      "StartMarketingDatePackage": "20160229",
      "SamplePackage": "N",
      "IndicationAndUsage": "helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun. ."
    },
    {
      "NDCCode": "15631-0104-4",
      "PackageDescription": "2500 PELLET in 1 PACKAGE (15631-0104-4) ",
      "NDC11Code": "15631-0104-04",
      "ProductNDC": "15631-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Cantharidinum",
      "NonProprietaryName": "Cantharidinum",
      "DosageFormName": "PELLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151006",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Rxhomeo Private Limited d.b.a. Rxhomeo, Inc",
      "SubstanceName": "CANTHARIDIN",
      "StrengthNumber": "8",
      "StrengthUnit": "[hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2022-01-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20180101",
      "SamplePackage": "N",
      "IndicationAndUsage": "Condition listed above or as directed by the physician."
    },
    {
      "NDCCode": "37662-0104-4",
      "PackageDescription": "10000 PELLET in 1 BOTTLE, GLASS (37662-0104-4) ",
      "NDC11Code": "37662-0104-04",
      "ProductNDC": "37662-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Calcarea Nitrica",
      "NonProprietaryName": "Calcarea Nitrica",
      "DosageFormName": "PELLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20220519",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Hahnemann Laboratories, INC.",
      "SubstanceName": "CALCIUM NITRITE",
      "StrengthNumber": "100",
      "StrengthUnit": "[hp_C]/1",
      "Status": "Active",
      "LastUpdate": "2022-05-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220519",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "38779-0104-4",
      "PackageDescription": "25 g in 1 BOTTLE, GLASS (38779-0104-4) ",
      "NDC11Code": "38779-0104-04",
      "ProductNDC": "38779-0104",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Methadone Hydrochloride",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20140812",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "Medisca Inc.",
      "SubstanceName": "METHADONE HYDROCHLORIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/g",
      "DEASchedule": "CII",
      "Status": "Unfinished",
      "LastUpdate": "2025-11-06",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "12-AUG-14"
    },
    {
      "NDCCode": "49288-0104-4",
      "PackageDescription": "30 mL in 1 VIAL, MULTI-DOSE (49288-0104-4)",
      "NDC11Code": "49288-0104-04",
      "ProductNDC": "49288-0104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Carrot",
      "NonProprietaryName": "Carrot",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRADERMAL; SUBCUTANEOUS",
      "StartMarketingDate": "19740323",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA102223",
      "LabelerName": "Antigen Laboratories, Inc.",
      "SubstanceName": "CARROT",
      "StrengthNumber": ".05",
      "StrengthUnit": "g/mL",
      "Pharm_Classes": "Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Vegetable Proteins [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Allergenic extract is used for diagnostic testing and for the treatment (immunotherapy) of patients whose histories indicate that upon natural exposure to the allergen, they experience allergic symptoms. Confirmation is determined by skin testing. Diagnostic use of allergenic extracts usually begins with direct skin testing. This product is not intended for treatment of patients who do not manifest immediate hypersensitivity reactions to the allergenic extract following skin testing.",
      "Description": "Antigen Laboratories’ allergenic extracts are manufactured from source material listed on the vial label. Lower concentrations (e.g. 1:50, 1:33, etc.) may be prepared either by dilution from a more concentrated stock or by direct extraction. The extract is a sterile solution containing extractables of source materials obtained from biological collecting and/or processing firms and Antigen Laboratories. All source materials are inspected by Antigen Laboratories’ technical personnel in accordance with 21 CFR 680.1 (b) (1). The route of administration for immunotherapy is subcutaneous. The routes of administration for diagnostic purposes are intradermal or prick-puncture of the skin. FOR ALLERGENIC EXTRACTS CONTAINING 50% V/V GLYCERINE AS PRESERVATIVE AND STABILIZER. INACTIVE INGREDIENTS. Sodium chloride…………………………………………………………….0.95%. Sodium bicarbonate………………………………………………………..0.24%. Glycerine…………………………………………………………………50% (v/v). Water for Injection…………………………………………………q.s. to volume. Active allergens are described by common and scientific name on the stock concentrate container label or on last page of this circular. Food allergenic extracts may be manufactured on a weight/volume (w/v) or volume/volume (v/v) basis. Food extracts made from dried raw material are extracted at 2-10% (1:50-1:10 w/v ratio) in extracting fluid containing 50% glycerine. Slurries of juicy fruits or vegetables (prepared with a minimum amount of water for injection) are combined with an equal volume of glycerine for a ration of 1:1 volume/volume (v/v). Sodium chloride and sodium bicarbonate are added to the slurry and glycerine mixture. Fresh egg white extract is prepared by adding one part raw egg white to nine parts of extracting fluid (1:9 v/v). Antigen E is considered the most important allergen of Short Ragweed pollen and is used for the standardization of Short Ragweed allergenic extracts. Stock mixtures containing Short Ragweed are analyzed for Antigen E content by radial immunodiffusion using Center for Biologics Evaluation and Research (CBER) references and anti-serum. Antigen E content expressed as units of Antigen E per milliliter (U/ml) is printed on container label."
    },
    {
      "NDCCode": "51552-0104-4",
      "PackageDescription": "25 g in 1 CONTAINER (51552-0104-4) ",
      "NDC11Code": "51552-0104-04",
      "ProductNDC": "51552-0104",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Testosterone Cypionate",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "19980401",
      "MarketingCategoryName": "BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING",
      "LabelerName": "Fagron Inc",
      "SubstanceName": "TESTOSTERONE CYPIONATE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/g",
      "DEASchedule": "CIII",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20221231",
      "StartMarketingDatePackage": "01-APR-98"
    },
    {
      "NDCCode": "51754-0104-7",
      "PackageDescription": "4 VIAL in 1 CARTON (51754-0104-7)  > 30 mL in 1 VIAL",
      "NDC11Code": "51754-0104-07",
      "ProductNDC": "51754-0104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Acetylcysteine",
      "NonProprietaryName": "Acetylcysteine Injection",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20210716",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA204797",
      "LabelerName": "Exela Pharma Sciences, LLC",
      "SubstanceName": "ACETYLCYSTEINE",
      "StrengthNumber": "200",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Antidote [EPC], Antidote for Acetaminophen Overdose [EPC], Decreased Respiratory Secretion Viscosity [PE], Increased Glutathione Concentration [PE], Mucolytic [EPC], Reduction Activity [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2025-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20210716",
      "SamplePackage": "N",
      "IndicationAndUsage": "Acetylcysteine injection is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI).",
      "Description": "Acetylcysteine injection is an intravenous antidote for the treatment of acetaminophen overdose. Acetylcysteine is the nonproprietary name for the N-acetyl derivative of the naturally occurring amino acid, L-cysteine (N-acetyl-L-cysteine). The compound is a white crystalline powder, which melts in the range of 104° to 110°C and has a very slight odor. The molecular formula of the compound is C5H9NO3S, and its molecular weight is 163.2. Acetylcysteine has the following structural formula:. Acetylcysteine injection is supplied as a sterile solution in vials containing 20% w/v (200 mg/mL) acetylcysteine. The pH of the solution ranges from 6.0 to 7.5. Acetylcysteine injection contains the following inactive ingredients: disodium edetate, sodium hydroxide (used for pH adjustment), and Sterile Water for Injection, USP."
    },
    {
      "NDCCode": "58232-0104-4",
      "PackageDescription": "29.5 mL in 1 TUBE (58232-0104-4) ",
      "NDC11Code": "58232-0104-04",
      "ProductNDC": "58232-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Aveeno Baby Daily Moisture",
      "NonProprietaryName": "Dimethicone",
      "DosageFormName": "LOTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20101201",
      "EndMarketingDate": "20201204",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "Johnson & Johnson Consumer Inc.",
      "SubstanceName": "DIMETHICONE",
      "StrengthNumber": "12",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-12-05",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20101201",
      "EndMarketingDatePackage": "20201204",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "58443-0104-4",
      "PackageDescription": "177 mL in 1 BOTTLE (58443-0104-4) ",
      "NDC11Code": "58443-0104-04",
      "ProductNDC": "58443-0104",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Solmate",
      "ProprietaryNameSuffix": "Broad Spectrum Spf 8",
      "NonProprietaryName": "Avobenzone, Octisalate, Octocrylene, And Oxybenzone",
      "DosageFormName": "LOTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130228",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Prime Enterprises, Inc.",
      "SubstanceName": "AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE",
      "StrengthNumber": "9.94; 29.84; 8.449; 9.94",
      "StrengthUnit": "mg/mL; 1/mL; mg/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2024-01-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20231231",
      "StartMarketingDatePackage": "20130228",
      "SamplePackage": "N",
      "IndicationAndUsage": "helps prevent sunburn."
    },
    {
      "NDCCode": "65096-0104-4",
      "PackageDescription": "5 kg in 1 CONTAINER (65096-0104-4) ",
      "NDC11Code": "65096-0104-04",
      "ProductNDC": "65096-0104",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Pioglitazone Hydrochloride",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20080101",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "Synthimed Labs Private Limited",
      "SubstanceName": "PIOGLITAZONE HYDROCHLORIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "kg/kg",
      "Status": "Unfinished",
      "LastUpdate": "2026-01-09",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "01-JAN-08"
    },
    {
      "NDCCode": "71335-0104-4",
      "PackageDescription": "30 TABLET in 1 BOTTLE (71335-0104-4) ",
      "NDC11Code": "71335-0104-04",
      "ProductNDC": "71335-0104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
      "NonProprietaryName": "Hydrocodone Bitartrate And Ibuprofen",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20100218",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA076642",
      "LabelerName": "Bryant Ranch Prepack",
      "SubstanceName": "HYDROCODONE BITARTRATE; IBUPROFEN",
      "StrengthNumber": "7.5; 200",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA]",
      "DEASchedule": "CII",
      "Status": "Deprecated",
      "LastUpdate": "2023-03-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20231231",
      "StartMarketingDatePackage": "20211227",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "0009-0104-04",
      "PackageDescription": "1 VIAL in 1 CARTON (0009-0104-04)  / 2 mL in 1 VIAL",
      "NDC11Code": "00009-0104-04",
      "ProductNDC": "0009-0104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Lincocin",
      "NonProprietaryName": "Lincomycin Hydrochloride",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAMUSCULAR; INTRAVENOUS; SUBCONJUNCTIVAL",
      "StartMarketingDate": "20230818",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA050317",
      "LabelerName": "Pharmacia & Upjohn Company LLC",
      "SubstanceName": "LINCOMYCIN HYDROCHLORIDE",
      "StrengthNumber": "300",
      "StrengthUnit": "mg/mL",
      "Status": "Active",
      "LastUpdate": "2025-03-13",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230818",
      "SamplePackage": "N",
      "IndicationAndUsage": "LINCOCIN is indicated in the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci. Its use should be reserved for penicillin-allergic patients or other patients for whom, in the judgment of the physician, a penicillin is inappropriate. Because of the risk of CDAD, as described in the BOXED WARNING, before selecting lincomycin the physician should consider the nature of the infection and the suitability of other alternatives. Indicated surgical procedures should be performed in conjunction with antibacterial therapy. LINCOCIN may be administered concomitantly with other antimicrobial agents when indicated. LINCOCIN is not indicated in the treatment of minor bacterial infections or viral infections. To reduce the development of drug-resistant bacteria and maintain the effectiveness of LINCOCIN and other antibacterial drugs, LINCOCIN 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.",
      "Description": "LINCOCIN (lincomycin injection, USP) is a sterile solution containing lincomycin hydrochloride which is the monohydrated salt of lincomycin, a lincosamide antibacterial produced by the growth of a member of the lincolnensis group of Streptomyces lincolnensis (Fam. Streptomycetaceae). The chemical name for lincomycin hydrochloride is Methyl 6,8-dideoxy-6-(1-methyl-trans-4-propyl-L-2-pyrolidinecarboxamido)-1-thio-D-erythro-α-D-galacto-octopyranoside monohydrochloride monohydrate. The molecular formula of lincomycin hydrochloride is C18H34N2O6S.HCl.H2O and the molecular weight is 461.01. The structural formula is represented below. Lincomycin hydrochloride is a white or practically white, crystalline powder and is odorless or has a faint odor. Its solutions are acid and are dextrorotatory. Lincomycin hydrochloride is freely soluble in water; soluble in dimethylformamide and very slightly soluble in acetone. LINCOCIN contains lincomycin hydrochloride in a sterile, clear, colorless solution with benzyl alcohol used as a preservative 9.45 mg/mL, and water for injection. LINCOCIN is a sterile solution for intramuscular and intravenous use. LINCOCIN is supplied in 2 mL and 10 mL multiple-dose vials containing 300 mg/mL of lincomycin (equivalent to 340 mg/mL of lincomycin hydrochloride, USP)."
    },
    {
      "NDCCode": "10122-104-01",
      "PackageDescription": "50 TABLET in 1 BLISTER PACK (10122-104-01) ",
      "NDC11Code": "10122-0104-01",
      "ProductNDC": "10122-104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Ferriprox",
      "NonProprietaryName": "Deferiprone",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20200519",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA212269",
      "LabelerName": "Chiesi USA, Inc.",
      "SubstanceName": "DEFERIPRONE",
      "StrengthNumber": "1000",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Iron Chelating Activity [MoA], Iron Chelator [EPC]",
      "Status": "Active",
      "LastUpdate": "2026-01-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20200519",
      "SamplePackage": "N",
      "IndicationAndUsage": "FERRIPROX Tablets are indicated for the treatment of transfusional iron overload in adult and pediatric patients 8 years of age and older with thalassemia syndromes, sickle cell disease or other anemias.       Limitations of Use.  Safety and effectiveness have not been established for the treatment of transfusional iron overload in patients with myelodysplastic syndrome or in patients with Diamond Blackfan anemia.",
      "Description": "FERRIPROX Tablets (deferiprone) contain 1,000 mg deferiprone (3-hydroxy-1,2-dimethylpyridin-4-one), a synthetic, orally active, iron-chelating agent. The molecular formula for deferiprone is C7H9NO2 and its molecular weight is 139.15 g/mol. Deferiprone has the following structural formula. Deferiprone is a white to pinkish-white powder. It is sparingly soluble in deionized water (14.3 mg/mL) and has a melting point range of 272 °C - 278 °C. FERRIPROX Tablets (twice a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “FPX” score “DR” on one side and “APO” score “1000” on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - hypromellose acetate succinate, magnesium oxide, colloidal silicon dioxide and magnesium stearate; Coating - triethyl citrate, talc, titanium dioxide, and methacrylic acid and ethyl acrylate copolymer. FERRIPROX Tablets (three times a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “APO” score “1000” on one side and plain on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - methylcellulose, crospovidone, and magnesium stearate; Coating - hypromellose, hydroxypropyl cellulose, macrogol, and titanium dioxide."
    },
    {
      "NDCCode": "10122-104-05",
      "PackageDescription": "50 TABLET in 1 BOTTLE, PLASTIC (10122-104-05) ",
      "NDC11Code": "10122-0104-05",
      "ProductNDC": "10122-104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Ferriprox",
      "NonProprietaryName": "Deferiprone",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20200519",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA212269",
      "LabelerName": "Chiesi USA, Inc.",
      "SubstanceName": "DEFERIPRONE",
      "StrengthNumber": "1000",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Iron Chelating Activity [MoA], Iron Chelator [EPC]",
      "Status": "Active",
      "LastUpdate": "2026-01-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20211201",
      "SamplePackage": "N",
      "IndicationAndUsage": "FERRIPROX Tablets are indicated for the treatment of transfusional iron overload in adult and pediatric patients 8 years of age and older with thalassemia syndromes, sickle cell disease or other anemias.       Limitations of Use.  Safety and effectiveness have not been established for the treatment of transfusional iron overload in patients with myelodysplastic syndrome or in patients with Diamond Blackfan anemia.",
      "Description": "FERRIPROX Tablets (deferiprone) contain 1,000 mg deferiprone (3-hydroxy-1,2-dimethylpyridin-4-one), a synthetic, orally active, iron-chelating agent. The molecular formula for deferiprone is C7H9NO2 and its molecular weight is 139.15 g/mol. Deferiprone has the following structural formula. Deferiprone is a white to pinkish-white powder. It is sparingly soluble in deionized water (14.3 mg/mL) and has a melting point range of 272 °C - 278 °C. FERRIPROX Tablets (twice a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “FPX” score “DR” on one side and “APO” score “1000” on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - hypromellose acetate succinate, magnesium oxide, colloidal silicon dioxide and magnesium stearate; Coating - triethyl citrate, talc, titanium dioxide, and methacrylic acid and ethyl acrylate copolymer. FERRIPROX Tablets (three times a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “APO” score “1000” on one side and plain on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - methylcellulose, crospovidone, and magnesium stearate; Coating - hypromellose, hydroxypropyl cellulose, macrogol, and titanium dioxide."
    }
  ]
}
                    

{"NDC":[{"NDCCode":"61626-0104-4","ProprietaryName":"Water","NonProprietaryName":"Aconitum Nap, Arsenicum Alb, Borax, Calc Phos, Gelsenium, Lycopodium, Phosphoricum Ac, Picricum Ac, Plumb Met, Solidago"},{"NDCCode":"61626-0098-4","ProprietaryName":"Flu Immune","NonProprietaryName":"Anas Barbarie Hepatis Et Cordis Extractum"},{"NDCCode":"61626-0099-4","ProprietaryName":"Pain Relief","NonProprietaryName":"Arnica, Chamomilla, Hypericum, Ignatia, Symphytum"},{"NDCCode":"61626-0100-4","ProprietaryName":"Day And Night Vitals","NonProprietaryName":"Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir"},{"NDCCode":"61626-0101-4","ProprietaryName":"Yin-yang Balance","NonProprietaryName":"Adamas, Agaricus Musc, Agnus, Aletris, Angelica Sin, Arg Nit, Arnica, Avena, Baryta, Graphites, Kali Brom, Kreosotum, Lycopodium, Ocimum Sanc, Phosphoricum Ac, Selenium, Sepia, Thuja Occ."},{"NDCCode":"61626-0102-4","ProprietaryName":"Earth","NonProprietaryName":"Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus."},{"NDCCode":"61626-0103-4","ProprietaryName":"Metal","NonProprietaryName":"Aluminia, Ammon Carb, Anacardium, Antimon Crud, Hydrastis, Ignatia, Mag Phos, Nat Mur, Nitricum Ac, Osmium, Paraffinum, Senna, Silicea, Spongia"},{"NDCCode":"61626-0105-4","ProprietaryName":"Wood","NonProprietaryName":"Belladonna, Berber Vulg, Carduus Mar, Chelidonium Maj, Cholesterinum, Colocynthis, Kali Carb, Nat Phos, Nitricum Ac, Nux Vom, Platinum Met, Sepia"},{"NDCCode":"61626-0106-4","ProprietaryName":"Fire","NonProprietaryName":"Apil Mel, Baptisia, Baryta Carb, Hamamelis, Kali Brom, Kali Phos, Lachesis, Lilium, Petroleum, Phosphoricum Ac, Spigelia Anth, Sulphur, Veratrum Vir"},{"NDCCode":"61626-0107-4","ProprietaryName":"Para Solve","NonProprietaryName":"Calc Carb, Chenopodium Anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc Corros, Nat Phos, Santoninum, Senna, Spigelia Anth, Stannum Met, Tanacetum, Teuricum Mar, Zingiber"},{"NDCCode":"61626-0108-4","ProprietaryName":"Flora Plus","NonProprietaryName":"Aloe, Alumina, Antimon Crud, Arg Nit, Chelidonium Maj, Gambogia, Graphites, Hydrastis, Lycopodium, Silicea"},{"NDCCode":"61626-0109-4","ProprietaryName":"Allergy","NonProprietaryName":"Allium Sat, Anacardium, Apis Mel, Gambogia, Merc Solub, Nat Carb, Nitricum Ac, Nux Vom, Phosphorus, Pulsatilla, Sulphur"},{"NDCCode":"61626-0110-4","ProprietaryName":"Er 911","NonProprietaryName":"Aconitum Nap, Apis Mel, Arnica, Arsenicum Alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus Canadensis, Clematis Erecta, Ferrum Phos, Histaminum, Hypericum, Ignatia, Impatiens Glan Flos, Ornithogalum, Passiflora, Phosphorus, Prunus Cerasifera, Rhus Tox, Sulphur, Symphytum, Vertarum Alb"},{"NDCCode":"61626-0111-4","ProprietaryName":"Scars-adhesions","NonProprietaryName":"Calc Fluor, Causticum, Graphites, Hydrofluoricum Ac, Lachesis, Plumb Met, Rhus Tox, Sepia, Silicea, Thiosinaminum"},{"NDCCode":"61626-0112-4","ProprietaryName":"Visceral Polarity","NonProprietaryName":"Aconitum Nap, Arg Nit, Chininum Pur, Echinacea Purp, Plum Met, Sepia, Sulphuricum Ac"},{"NDCCode":"11523-0104-4","ProprietaryName":"Claritin","NonProprietaryName":"Loratadine"},{"NDCCode":"13630-0104-4","ProprietaryName":"Miami Beach","NonProprietaryName":"Avobenzone, Homosalate, Octisalate, And Octocrylene"},{"NDCCode":"15631-0104-4","ProprietaryName":"Cantharidinum","NonProprietaryName":"Cantharidinum"},{"NDCCode":"37662-0104-4","ProprietaryName":"Calcarea Nitrica","NonProprietaryName":"Calcarea Nitrica"},{"NDCCode":"38779-0104-4","NonProprietaryName":"Methadone Hydrochloride"},{"NDCCode":"49288-0104-4","ProprietaryName":"Carrot","NonProprietaryName":"Carrot"},{"NDCCode":"51552-0104-4","NonProprietaryName":"Testosterone Cypionate"},{"NDCCode":"51754-0104-7","ProprietaryName":"Acetylcysteine","NonProprietaryName":"Acetylcysteine Injection"},{"NDCCode":"58232-0104-4","ProprietaryName":"Aveeno Baby Daily Moisture","NonProprietaryName":"Dimethicone"},{"NDCCode":"58443-0104-4","ProprietaryName":"Solmate","NonProprietaryName":"Avobenzone, Octisalate, Octocrylene, And Oxybenzone"},{"NDCCode":"65096-0104-4","NonProprietaryName":"Pioglitazone Hydrochloride"},{"NDCCode":"71335-0104-4","ProprietaryName":"Hydrocodone Bitartrate And Ibuprofen","NonProprietaryName":"Hydrocodone Bitartrate And Ibuprofen"},{"NDCCode":"0009-0104-04","ProprietaryName":"Lincocin","NonProprietaryName":"Lincomycin Hydrochloride"},{"NDCCode":"10122-104-01","ProprietaryName":"Ferriprox","NonProprietaryName":"Deferiprone"},{"NDCCode":"10122-104-05","ProprietaryName":"Ferriprox","NonProprietaryName":"Deferiprone"}]}
                    

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  <NDC>
    <NDCCode>61626-0104-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0104-4) </PackageDescription>
    <NDC11Code>61626-0104-04</NDC11Code>
    <ProductNDC>61626-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Water</ProprietaryName>
    <NonProprietaryName>Aconitum Nap, Arsenicum Alb, Borax, Calc Phos, Gelsenium, Lycopodium, Phosphoricum Ac, Picricum Ac, Plumb Met, Solidago</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; ARSENIC TRIOXIDE; SODIUM BORATE; TRIBASIC CALCIUM PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; LYCOPODIUM CLAVATUM SPORE; PHOSPHORIC ACID; PICRIC ACID; LEAD; SOLIDAGO VIRGAUREA FLOWERING TOP</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Pharm_Classes>Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of fear, weak - paralyzed will, dread, and related emotions. Sensory, spinal and extremity disorders. Ear - earache, bone - occipital and neck pain, weak spine and lower extremity disorders.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0098-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0098-4) </PackageDescription>
    <NDC11Code>61626-0098-04</NDC11Code>
    <ProductNDC>61626-0098</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Flu Immune</ProprietaryName>
    <NonProprietaryName>Anas Barbarie Hepatis Et Cordis Extractum</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE</SubstanceName>
    <StrengthNumber>200</StrengthNumber>
    <StrengthUnit>[hp_C]/59mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of flu-related symptoms such as aches, pains, fever and chills. Flu Immune can be used at the onset of flu-like symptoms and as preventative. Flu Immune helps stimulate the body's immunity and is reccommended as first line of defense against flu-like symptoms. **.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0099-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0099-4) </PackageDescription>
    <NDC11Code>61626-0099-04</NDC11Code>
    <ProductNDC>61626-0099</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Pain Relief</ProprietaryName>
    <NonProprietaryName>Arnica, Chamomilla, Hypericum, Ignatia, Symphytum</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ARNICA MONTANA; MATRICARIA CHAMOMILLA; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; COMFREY ROOT</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of general pain, includingm symptoms related to joints, bones, muscles, minor bruises, spinal pain and pain due to arthiritis. **.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0100-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0100-4) </PackageDescription>
    <NDC11Code>61626-0100-04</NDC11Code>
    <ProductNDC>61626-0100</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Day And Night Vitals</ProprietaryName>
    <NonProprietaryName>Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>GARLIC; ALOE VERA LEAF; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; TRIBASIC CALCIUM PHOSPHATE; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; CHOLESTEROL; CLEMATIS RECTA FLOWERING TOP; MARSDENIA CONDURANGO BARK; GAMBOGE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; POTASSIUM BROMIDE; DIBASIC POTASSIUM PHOSPHATE; LYCOPODIUM CLAVATUM SPORE; SODIUM CARBONATE; PASSIFLORA INCARNATA TOP; SENNA LEAF; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SPIGELIA ANTHELMIA; SPONGIA OFFICINALIS SKELETON, ROASTED; VERATRUM VIRIDE ROOT</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
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    <Pharm_Classes>Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of symptoms related to low vitality and function of the Large intestine, Stomach, Spleen, Heart, Small Intestine, Bladder, Kidney, Sex Organs, Thyroid, Adrenal, Gall Bladder, Liver and Lung.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0101-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0101-4) </PackageDescription>
    <NDC11Code>61626-0101-04</NDC11Code>
    <ProductNDC>61626-0101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Yin-yang Balance</ProprietaryName>
    <NonProprietaryName>Adamas, Agaricus Musc, Agnus, Aletris, Angelica Sin, Arg Nit, Arnica, Avena, Baryta, Graphites, Kali Brom, Kreosotum, Lycopodium, Ocimum Sanc, Phosphoricum Ac, Selenium, Sepia, Thuja Occ.</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>DIAMOND; AMANITA MUSCARIA FRUITING BODY; CHASTE TREE; ALETRIS FARINOSA ROOT; ANGELICA SINENSIS ROOT; SILVER NITRATE; ARNICA MONTANA; AVENA SATIVA FLOWERING TOP; BARIUM IODIDE; GRAPHITE; POTASSIUM BROMIDE; WOOD CREOSOTE; LYCOPODIUM CLAVATUM SPORE; OCIMUM TENUIFLORUM TOP; PHOSPHORIC ACID; SELENIUM; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of hormonal disbalance in men and women.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0102-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0102-4) </PackageDescription>
    <NDC11Code>61626-0102-04</NDC11Code>
    <ProductNDC>61626-0102</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Earth</ProprietaryName>
    <NonProprietaryName>Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus.</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>GOLD; SILVER NITRATE; CAUSTICUM; CINCHONA OFFICINALIS BARK; MARSDENIA CONDURANGO BARK; CEANOTHUS AMERICANUS LEAF; EUPHRASIA STRICTA; FUCUS VESICULOSUS; GALLIC ACID MONOHYDRATE; IRIS VERSICOLOR ROOT; SODIUM CARBONATE; NITRIC ACID; PHOSPHORUS</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE. For the temporary relief of the neuro-emotional (automatic nervous system - non psychiatric) disorders of oversympathy, low self esteem and related emotions. Sensory, spinal and extremity disorders. Relief of symptoms of colds, sinus problems. Digestive, mouth saliva, taste disorders. Weak spine and lower extremity disorders.**​.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0103-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0103-4) </PackageDescription>
    <NDC11Code>61626-0103-04</NDC11Code>
    <ProductNDC>61626-0103</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Metal</ProprietaryName>
    <NonProprietaryName>Aluminia, Ammon Carb, Anacardium, Antimon Crud, Hydrastis, Ignatia, Mag Phos, Nat Mur, Nitricum Ac, Osmium, Paraffinum, Senna, Silicea, Spongia</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ALUMINUM OXIDE; AMMONIUM CARBONATE; ANACARDIUM OCCIDENTALE FRUIT; ANTIMONY TRISULFIDE; GOLDENSEAL; STRYCHNOS IGNATII SEED; MAGNESIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; NITRIC ACID; OSMIUM; PARAFFIN; SENNA LEAF; SILICON DIOXIDE; SPONGIA OFFICINALIS SKELETON, ROASTED</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE. For the temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of grief, dogmatically positioned, sadness, crying, and related emotions. Sensory, spinal and extremity disorders. Nose - smell, mucous. Constipation. Skin - dry, itching. Weak spine disorders.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0105-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0105-4) </PackageDescription>
    <NDC11Code>61626-0105-04</NDC11Code>
    <ProductNDC>61626-0105</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Wood</ProprietaryName>
    <NonProprietaryName>Belladonna, Berber Vulg, Carduus Mar, Chelidonium Maj, Cholesterinum, Colocynthis, Kali Carb, Nat Phos, Nitricum Ac, Nux Vom, Platinum Met, Sepia</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ATROPA BELLADONNA; BERBERIS VULGARIS ROOT BARK; MILK THISTLE; CHELIDONIUM MAJUS; CHOLESTEROL; CITRULLUS COLOCYNTHIS FRUIT PULP; POTASSIUM CARBONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PLATINUM; SEPIA OFFICINALIS JUICE</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non phychiatric) disorders of anger, resentment and related emotions. Temporary relief of headache symptoms. Billousness, eye - minor eye irritation, tears, muscle, neck, weak spine and lower extremity disorders.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0106-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0106-4) </PackageDescription>
    <NDC11Code>61626-0106-04</NDC11Code>
    <ProductNDC>61626-0106</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Fire</ProprietaryName>
    <NonProprietaryName>Apil Mel, Baptisia, Baryta Carb, Hamamelis, Kali Brom, Kali Phos, Lachesis, Lilium, Petroleum, Phosphoricum Ac, Spigelia Anth, Sulphur, Veratrum Vir</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; POTASSIUM BROMIDE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; LILIUM LANCIFOLIUM BULB; KEROSENE; PHOSPHORIC ACID; SPIGELIA ANTHELMIA; SULFUR; VERATRUM VIRIDE ROOT</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For temporary relief of the neuro-emotional (autonomic nervous system - non psychiatric) disorders of vulnerability, lost, and related emotions. Minor circulation irregularities, fatigue. Tongue, perspiration, spine, and upper extremity disorders. Temporary relief of chest congestion and minor pain in reproductive organs.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0107-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0107-4) </PackageDescription>
    <NDC11Code>61626-0107-04</NDC11Code>
    <ProductNDC>61626-0107</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Para Solve</ProprietaryName>
    <NonProprietaryName>Calc Carb, Chenopodium Anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc Corros, Nat Phos, Santoninum, Senna, Spigelia Anth, Stannum Met, Tanacetum, Teuricum Mar, Zingiber</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>OYSTER SHELL CALCIUM CARBONATE, CRUDE; DYSPHANIA AMBROSIOIDES; ARTEMISIA CINA PRE-FLOWERING TOP; CROTON TIGLIUM SEED; DRYOPTERIS FILIX-MAS ROOT; GAMBOGE; PUNICA GRANATUM ROOT BARK; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SANTONIN; SENNA LEAF; SPIGELIA ANTHELMIA; TIN; TANACETUM VULGARE TOP; TEUCRIUM MARUM; GINGER</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], 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>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE​: For the temporary relief of gastrointestinal symptoms such as gas, bloating, stomach upset, abdominal discomfort which may be accompanied  by pale face or circles under the eyes, bad breath, bariable appetite, localized ithching, postnasal drip, canker sores. irritability, back pain, resltess sleep, and sensitivity in lower right abdominal area. Temporary relief of cough.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0108-4</NDCCode>
    <PackageDescription>59.1 mL in 1 BOTTLE (61626-0108-4) </PackageDescription>
    <NDC11Code>61626-0108-04</NDC11Code>
    <ProductNDC>61626-0108</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Flora Plus</ProprietaryName>
    <NonProprietaryName>Aloe, Alumina, Antimon Crud, Arg Nit, Chelidonium Maj, Gambogia, Graphites, Hydrastis, Lycopodium, Silicea</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ALOE VERA LEAF; ALUMINUM OXIDE; ANTIMONY TRISULFIDE; SILVER NITRATE; CHELIDONIUM MAJUS; GAMBOGE; GRAPHITE; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; SILICON DIOXIDE</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For temporary relief of bowel congestions-constipation, gas, bloating  Digestive disturbance and intestinal complaints from bread, acids, sour wines, fermentable foods-sweets-yeast  ​​ White or yellow film on tongue  ​ Relief of symptoms associated with yeast infections  Sensitivity in lower right abdominal area. **.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0109-4</NDCCode>
    <PackageDescription>59.1 mL in 1 BOTTLE (61626-0109-4) </PackageDescription>
    <NDC11Code>61626-0109-04</NDC11Code>
    <ProductNDC>61626-0109</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Allergy</ProprietaryName>
    <NonProprietaryName>Allium Sat, Anacardium, Apis Mel, Gambogia, Merc Solub, Nat Carb, Nitricum Ac, Nux Vom, Phosphorus, Pulsatilla, Sulphur</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Net Remedies</LabelerName>
    <SubstanceName>GARLIC; ANACARDIUM OCCIDENTALE FRUIT; APIS MELLIFERA; GAMBOGE; MERCURIUS SOLUBILIS; SODIUM CARBONATE; NITRIC ACID; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; ANEMONE PULSATILLA; SULFUR</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: For the temporary relief of allergic reactions from environmental agents, slight errors in diet or certain foods causing symptoms of sensitivity, mood changes, headaches, tiredness, sinus congestion, itchy or burning eyes, dyspepsia, bloating, gas, sensitivity in lower right abdominal area.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0110-4</NDCCode>
    <PackageDescription>59.1 mL in 1 BOTTLE (61626-0110-4) </PackageDescription>
    <NDC11Code>61626-0110-04</NDC11Code>
    <ProductNDC>61626-0110</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Er 911</ProprietaryName>
    <NonProprietaryName>Aconitum Nap, Apis Mel, Arnica, Arsenicum Alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus Canadensis, Clematis Erecta, Ferrum Phos, Histaminum, Hypericum, Ignatia, Impatiens Glan Flos, Ornithogalum, Passiflora, Phosphorus, Prunus Cerasifera, Rhus Tox, Sulphur, Symphytum, Vertarum Alb</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Net Remedies</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; APIS MELLIFERA; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA CHAMOMILLA; HELIANTHEMUM CANADENSE; CLEMATIS RECTA FLOWERING TOP; FERROSOFERRIC PHOSPHATE; HISTAMINE DIHYDROCHLORIDE; HYPERICUM PERFORATUM; STRYCHNOS IGNATII SEED; IMPATIENS GLANDULIFERA FLOWER; ORNITHOGALUM UMBELLATUM; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; PRUNUS CERASIFERA FLOWER; TOXICODENDRON PUBESCENS LEAF; SULFUR; COMFREY ROOT; VERATRUM ALBUM ROOT</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: For the temporary relief of emotional, mental, or physical trauma, high pressure or stressful situations  Symptomatic relief of nervous tension, stress, dread and fever. Temporary relief of cold and flu-like symptoms. Overexertion ​​ Strains  Tearfulness  Fearfulness  Oversensitivity  Minor nerve pain and burning  ​ Quieting effect on nervous system.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0111-4</NDCCode>
    <PackageDescription>59.1 mL in 1 BOTTLE (61626-0111-4) </PackageDescription>
    <NDC11Code>61626-0111-04</NDC11Code>
    <ProductNDC>61626-0111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Scars-adhesions</ProprietaryName>
    <NonProprietaryName>Calc Fluor, Causticum, Graphites, Hydrofluoricum Ac, Lachesis, Plumb Met, Rhus Tox, Sepia, Silicea, Thiosinaminum</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>CALCIUM FLUORIDE; CAUSTICUM; GRAPHITE; HYDROFLUORIC ACID; LACHESIS MUTA VENOM; LEAD; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; ALLYLTHIOUREA</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​Helps absorption of scars-fibrous tissue adhesions  For the temporary relief of itching of scars  Feelins of spasm pressure and tightness sensation in internal organs, esophagus and stomach  ​​ Colic type symptoms.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>61626-0112-4</NDCCode>
    <PackageDescription>59 mL in 1 BOTTLE (61626-0112-4) </PackageDescription>
    <NDC11Code>61626-0112-04</NDC11Code>
    <ProductNDC>61626-0112</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Visceral Polarity</ProprietaryName>
    <NonProprietaryName>Aconitum Nap, Arg Nit, Chininum Pur, Echinacea Purp, Plum Met, Sepia, Sulphuricum Ac</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20181204</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>NET Remedies</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; SILVER NITRATE; QUININE; ECHINACEA PURPUREA; FERRIC FERROCYANIDE; GELSEMIUM SEMPERVIRENS ROOT; HOPS; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; LEAD; SEPIA OFFICINALIS JUICE; SULFURIC ACID</SubstanceName>
    <StrengthNumber>12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Allergens [CS], Antimalarial [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Chelating Activity [MoA], Decorporation Agent [EPC], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2021-01-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181204</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>​INDICATIONS FOR USE: ​For the temporary relief of lack of general emotional, physical, or mental balance  Minor nervous system tension, confusion, nervousness, fatigue  ​​ Feelings of spasm pressure and tightness sensation in internal organs, esophagus and stomach  Temporary relief of heartburn ​ General tone of nervous and digestive systems.**.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>11523-0104-4</NDCCode>
    <PackageDescription>4 BLISTER PACK in 1 CARTON (11523-0104-4)  / 10 TABLET, CHEWABLE in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>11523-0104-04</NDC11Code>
    <ProductNDC>11523-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Claritin</ProprietaryName>
    <NonProprietaryName>Loratadine</NonProprietaryName>
    <DosageFormName>TABLET, CHEWABLE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20230205</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA210033</ApplicationNumber>
    <LabelerName>Bayer HealthCare LLC.</LabelerName>
    <SubstanceName>LORATADINE</SubstanceName>
    <StrengthNumber>5</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-12-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230208</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: 1 runny nose, 2 sneezing, 3 itchy, watery eyes, 4 itching of the nose or throat.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>13630-0104-4</NDCCode>
    <PackageDescription>177 mL in 1 CAN (13630-0104-4) </PackageDescription>
    <NDC11Code>13630-0104-04</NDC11Code>
    <ProductNDC>13630-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Miami Beach</ProprietaryName>
    <ProprietaryNameSuffix>Spf 50 Kids C/s Sunscreen</ProprietaryNameSuffix>
    <NonProprietaryName>Avobenzone, Homosalate, Octisalate, And Octocrylene</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20160229</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Prime Packaging Inc.</LabelerName>
    <SubstanceName>AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE</SubstanceName>
    <StrengthNumber>30.66; 102.2; 51.1; 28.11</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL; mg/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2023-01-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20221231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20160229</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun. .</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>15631-0104-4</NDCCode>
    <PackageDescription>2500 PELLET in 1 PACKAGE (15631-0104-4) </PackageDescription>
    <NDC11Code>15631-0104-04</NDC11Code>
    <ProductNDC>15631-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Cantharidinum</ProprietaryName>
    <NonProprietaryName>Cantharidinum</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151006</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Rxhomeo Private Limited d.b.a. Rxhomeo, Inc</LabelerName>
    <SubstanceName>CANTHARIDIN</SubstanceName>
    <StrengthNumber>8</StrengthNumber>
    <StrengthUnit>[hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2022-01-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Condition listed above or as directed by the physician.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>37662-0104-4</NDCCode>
    <PackageDescription>10000 PELLET in 1 BOTTLE, GLASS (37662-0104-4) </PackageDescription>
    <NDC11Code>37662-0104-04</NDC11Code>
    <ProductNDC>37662-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Calcarea Nitrica</ProprietaryName>
    <NonProprietaryName>Calcarea Nitrica</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20220519</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Hahnemann Laboratories, INC.</LabelerName>
    <SubstanceName>CALCIUM NITRITE</SubstanceName>
    <StrengthNumber>100</StrengthNumber>
    <StrengthUnit>[hp_C]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2022-05-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220519</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>38779-0104-4</NDCCode>
    <PackageDescription>25 g in 1 BOTTLE, GLASS (38779-0104-4) </PackageDescription>
    <NDC11Code>38779-0104-04</NDC11Code>
    <ProductNDC>38779-0104</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Methadone Hydrochloride</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20140812</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>Medisca Inc.</LabelerName>
    <SubstanceName>METHADONE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <DEASchedule>CII</DEASchedule>
    <Status>Unfinished</Status>
    <LastUpdate>2025-11-06</LastUpdate>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>12-AUG-14</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>49288-0104-4</NDCCode>
    <PackageDescription>30 mL in 1 VIAL, MULTI-DOSE (49288-0104-4)</PackageDescription>
    <NDC11Code>49288-0104-04</NDC11Code>
    <ProductNDC>49288-0104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Carrot</ProprietaryName>
    <NonProprietaryName>Carrot</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRADERMAL; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>19740323</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA102223</ApplicationNumber>
    <LabelerName>Antigen Laboratories, Inc.</LabelerName>
    <SubstanceName>CARROT</SubstanceName>
    <StrengthNumber>.05</StrengthNumber>
    <StrengthUnit>g/mL</StrengthUnit>
    <Pharm_Classes>Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Vegetable Proteins [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Allergenic extract is used for diagnostic testing and for the treatment (immunotherapy) of patients whose histories indicate that upon natural exposure to the allergen, they experience allergic symptoms. Confirmation is determined by skin testing. Diagnostic use of allergenic extracts usually begins with direct skin testing. This product is not intended for treatment of patients who do not manifest immediate hypersensitivity reactions to the allergenic extract following skin testing.</IndicationAndUsage>
    <Description>Antigen Laboratories’ allergenic extracts are manufactured from source material listed on the vial label. Lower concentrations (e.g. 1:50, 1:33, etc.) may be prepared either by dilution from a more concentrated stock or by direct extraction. The extract is a sterile solution containing extractables of source materials obtained from biological collecting and/or processing firms and Antigen Laboratories. All source materials are inspected by Antigen Laboratories’ technical personnel in accordance with 21 CFR 680.1 (b) (1). The route of administration for immunotherapy is subcutaneous. The routes of administration for diagnostic purposes are intradermal or prick-puncture of the skin. FOR ALLERGENIC EXTRACTS CONTAINING 50% V/V GLYCERINE AS PRESERVATIVE AND STABILIZER. INACTIVE INGREDIENTS. Sodium chloride…………………………………………………………….0.95%. Sodium bicarbonate………………………………………………………..0.24%. Glycerine…………………………………………………………………50% (v/v). Water for Injection…………………………………………………q.s. to volume. Active allergens are described by common and scientific name on the stock concentrate container label or on last page of this circular. Food allergenic extracts may be manufactured on a weight/volume (w/v) or volume/volume (v/v) basis. Food extracts made from dried raw material are extracted at 2-10% (1:50-1:10 w/v ratio) in extracting fluid containing 50% glycerine. Slurries of juicy fruits or vegetables (prepared with a minimum amount of water for injection) are combined with an equal volume of glycerine for a ration of 1:1 volume/volume (v/v). Sodium chloride and sodium bicarbonate are added to the slurry and glycerine mixture. Fresh egg white extract is prepared by adding one part raw egg white to nine parts of extracting fluid (1:9 v/v). Antigen E is considered the most important allergen of Short Ragweed pollen and is used for the standardization of Short Ragweed allergenic extracts. Stock mixtures containing Short Ragweed are analyzed for Antigen E content by radial immunodiffusion using Center for Biologics Evaluation and Research (CBER) references and anti-serum. Antigen E content expressed as units of Antigen E per milliliter (U/ml) is printed on container label.</Description>
  </NDC>
  <NDC>
    <NDCCode>51552-0104-4</NDCCode>
    <PackageDescription>25 g in 1 CONTAINER (51552-0104-4) </PackageDescription>
    <NDC11Code>51552-0104-04</NDC11Code>
    <ProductNDC>51552-0104</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Testosterone Cypionate</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>19980401</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING</MarketingCategoryName>
    <LabelerName>Fagron Inc</LabelerName>
    <SubstanceName>TESTOSTERONE CYPIONATE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <DEASchedule>CIII</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20221231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>01-APR-98</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>51754-0104-7</NDCCode>
    <PackageDescription>4 VIAL in 1 CARTON (51754-0104-7)  &gt; 30 mL in 1 VIAL</PackageDescription>
    <NDC11Code>51754-0104-07</NDC11Code>
    <ProductNDC>51754-0104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Acetylcysteine</ProprietaryName>
    <NonProprietaryName>Acetylcysteine Injection</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20210716</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA204797</ApplicationNumber>
    <LabelerName>Exela Pharma Sciences, LLC</LabelerName>
    <SubstanceName>ACETYLCYSTEINE</SubstanceName>
    <StrengthNumber>200</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Antidote [EPC], Antidote for Acetaminophen Overdose [EPC], Decreased Respiratory Secretion Viscosity [PE], Increased Glutathione Concentration [PE], Mucolytic [EPC], Reduction Activity [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2025-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20210716</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Acetylcysteine injection is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI).</IndicationAndUsage>
    <Description>Acetylcysteine injection is an intravenous antidote for the treatment of acetaminophen overdose. Acetylcysteine is the nonproprietary name for the N-acetyl derivative of the naturally occurring amino acid, L-cysteine (N-acetyl-L-cysteine). The compound is a white crystalline powder, which melts in the range of 104° to 110°C and has a very slight odor. The molecular formula of the compound is C5H9NO3S, and its molecular weight is 163.2. Acetylcysteine has the following structural formula:. Acetylcysteine injection is supplied as a sterile solution in vials containing 20% w/v (200 mg/mL) acetylcysteine. The pH of the solution ranges from 6.0 to 7.5. Acetylcysteine injection contains the following inactive ingredients: disodium edetate, sodium hydroxide (used for pH adjustment), and Sterile Water for Injection, USP.</Description>
  </NDC>
  <NDC>
    <NDCCode>58232-0104-4</NDCCode>
    <PackageDescription>29.5 mL in 1 TUBE (58232-0104-4) </PackageDescription>
    <NDC11Code>58232-0104-04</NDC11Code>
    <ProductNDC>58232-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Aveeno Baby Daily Moisture</ProprietaryName>
    <NonProprietaryName>Dimethicone</NonProprietaryName>
    <DosageFormName>LOTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20101201</StartMarketingDate>
    <EndMarketingDate>20201204</EndMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>Johnson &amp; Johnson Consumer Inc.</LabelerName>
    <SubstanceName>DIMETHICONE</SubstanceName>
    <StrengthNumber>12</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-12-05</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20101201</StartMarketingDatePackage>
    <EndMarketingDatePackage>20201204</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>58443-0104-4</NDCCode>
    <PackageDescription>177 mL in 1 BOTTLE (58443-0104-4) </PackageDescription>
    <NDC11Code>58443-0104-04</NDC11Code>
    <ProductNDC>58443-0104</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Solmate</ProprietaryName>
    <ProprietaryNameSuffix>Broad Spectrum Spf 8</ProprietaryNameSuffix>
    <NonProprietaryName>Avobenzone, Octisalate, Octocrylene, And Oxybenzone</NonProprietaryName>
    <DosageFormName>LOTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130228</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Prime Enterprises, Inc.</LabelerName>
    <SubstanceName>AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE</SubstanceName>
    <StrengthNumber>9.94; 29.84; 8.449; 9.94</StrengthNumber>
    <StrengthUnit>mg/mL; 1/mL; mg/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-01-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20231231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20130228</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>helps prevent sunburn.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>65096-0104-4</NDCCode>
    <PackageDescription>5 kg in 1 CONTAINER (65096-0104-4) </PackageDescription>
    <NDC11Code>65096-0104-04</NDC11Code>
    <ProductNDC>65096-0104</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Pioglitazone Hydrochloride</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20080101</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>Synthimed Labs Private Limited</LabelerName>
    <SubstanceName>PIOGLITAZONE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>kg/kg</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2026-01-09</LastUpdate>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>01-JAN-08</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>71335-0104-4</NDCCode>
    <PackageDescription>30 TABLET in 1 BOTTLE (71335-0104-4) </PackageDescription>
    <NDC11Code>71335-0104-04</NDC11Code>
    <ProductNDC>71335-0104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Hydrocodone Bitartrate And Ibuprofen</ProprietaryName>
    <NonProprietaryName>Hydrocodone Bitartrate And Ibuprofen</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20100218</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA076642</ApplicationNumber>
    <LabelerName>Bryant Ranch Prepack</LabelerName>
    <SubstanceName>HYDROCODONE BITARTRATE; IBUPROFEN</SubstanceName>
    <StrengthNumber>7.5; 200</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Opioid Agonist [EPC], Opioid Agonists [MoA]</Pharm_Classes>
    <DEASchedule>CII</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2023-03-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20231231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20211227</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>0009-0104-04</NDCCode>
    <PackageDescription>1 VIAL in 1 CARTON (0009-0104-04)  / 2 mL in 1 VIAL</PackageDescription>
    <NDC11Code>00009-0104-04</NDC11Code>
    <ProductNDC>0009-0104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Lincocin</ProprietaryName>
    <NonProprietaryName>Lincomycin Hydrochloride</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAMUSCULAR; INTRAVENOUS; SUBCONJUNCTIVAL</RouteName>
    <StartMarketingDate>20230818</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA050317</ApplicationNumber>
    <LabelerName>Pharmacia &amp; Upjohn Company LLC</LabelerName>
    <SubstanceName>LINCOMYCIN HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>300</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-03-13</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230818</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>LINCOCIN is indicated in the treatment of serious infections due to susceptible strains of streptococci, pneumococci, and staphylococci. Its use should be reserved for penicillin-allergic patients or other patients for whom, in the judgment of the physician, a penicillin is inappropriate. Because of the risk of CDAD, as described in the BOXED WARNING, before selecting lincomycin the physician should consider the nature of the infection and the suitability of other alternatives. Indicated surgical procedures should be performed in conjunction with antibacterial therapy. LINCOCIN may be administered concomitantly with other antimicrobial agents when indicated. LINCOCIN is not indicated in the treatment of minor bacterial infections or viral infections. To reduce the development of drug-resistant bacteria and maintain the effectiveness of LINCOCIN and other antibacterial drugs, LINCOCIN 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.</IndicationAndUsage>
    <Description>LINCOCIN (lincomycin injection, USP) is a sterile solution containing lincomycin hydrochloride which is the monohydrated salt of lincomycin, a lincosamide antibacterial produced by the growth of a member of the lincolnensis group of Streptomyces lincolnensis (Fam. Streptomycetaceae). The chemical name for lincomycin hydrochloride is Methyl 6,8-dideoxy-6-(1-methyl-trans-4-propyl-L-2-pyrolidinecarboxamido)-1-thio-D-erythro-α-D-galacto-octopyranoside monohydrochloride monohydrate. The molecular formula of lincomycin hydrochloride is C18H34N2O6S.HCl.H2O and the molecular weight is 461.01. The structural formula is represented below. Lincomycin hydrochloride is a white or practically white, crystalline powder and is odorless or has a faint odor. Its solutions are acid and are dextrorotatory. Lincomycin hydrochloride is freely soluble in water; soluble in dimethylformamide and very slightly soluble in acetone. LINCOCIN contains lincomycin hydrochloride in a sterile, clear, colorless solution with benzyl alcohol used as a preservative 9.45 mg/mL, and water for injection. LINCOCIN is a sterile solution for intramuscular and intravenous use. LINCOCIN is supplied in 2 mL and 10 mL multiple-dose vials containing 300 mg/mL of lincomycin (equivalent to 340 mg/mL of lincomycin hydrochloride, USP).</Description>
  </NDC>
  <NDC>
    <NDCCode>10122-104-01</NDCCode>
    <PackageDescription>50 TABLET in 1 BLISTER PACK (10122-104-01) </PackageDescription>
    <NDC11Code>10122-0104-01</NDC11Code>
    <ProductNDC>10122-104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Ferriprox</ProprietaryName>
    <NonProprietaryName>Deferiprone</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20200519</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA212269</ApplicationNumber>
    <LabelerName>Chiesi USA, Inc.</LabelerName>
    <SubstanceName>DEFERIPRONE</SubstanceName>
    <StrengthNumber>1000</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Iron Chelating Activity [MoA], Iron Chelator [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-01-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20200519</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>FERRIPROX Tablets are indicated for the treatment of transfusional iron overload in adult and pediatric patients 8 years of age and older with thalassemia syndromes, sickle cell disease or other anemias.       Limitations of Use.  Safety and effectiveness have not been established for the treatment of transfusional iron overload in patients with myelodysplastic syndrome or in patients with Diamond Blackfan anemia.</IndicationAndUsage>
    <Description>FERRIPROX Tablets (deferiprone) contain 1,000 mg deferiprone (3-hydroxy-1,2-dimethylpyridin-4-one), a synthetic, orally active, iron-chelating agent. The molecular formula for deferiprone is C7H9NO2 and its molecular weight is 139.15 g/mol. Deferiprone has the following structural formula. Deferiprone is a white to pinkish-white powder. It is sparingly soluble in deionized water (14.3 mg/mL) and has a melting point range of 272 °C - 278 °C. FERRIPROX Tablets (twice a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “FPX” score “DR” on one side and “APO” score “1000” on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - hypromellose acetate succinate, magnesium oxide, colloidal silicon dioxide and magnesium stearate; Coating - triethyl citrate, talc, titanium dioxide, and methacrylic acid and ethyl acrylate copolymer. FERRIPROX Tablets (three times a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “APO” score “1000” on one side and plain on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - methylcellulose, crospovidone, and magnesium stearate; Coating - hypromellose, hydroxypropyl cellulose, macrogol, and titanium dioxide.</Description>
  </NDC>
  <NDC>
    <NDCCode>10122-104-05</NDCCode>
    <PackageDescription>50 TABLET in 1 BOTTLE, PLASTIC (10122-104-05) </PackageDescription>
    <NDC11Code>10122-0104-05</NDC11Code>
    <ProductNDC>10122-104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Ferriprox</ProprietaryName>
    <NonProprietaryName>Deferiprone</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20200519</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA212269</ApplicationNumber>
    <LabelerName>Chiesi USA, Inc.</LabelerName>
    <SubstanceName>DEFERIPRONE</SubstanceName>
    <StrengthNumber>1000</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Iron Chelating Activity [MoA], Iron Chelator [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-01-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20211201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>FERRIPROX Tablets are indicated for the treatment of transfusional iron overload in adult and pediatric patients 8 years of age and older with thalassemia syndromes, sickle cell disease or other anemias.       Limitations of Use.  Safety and effectiveness have not been established for the treatment of transfusional iron overload in patients with myelodysplastic syndrome or in patients with Diamond Blackfan anemia.</IndicationAndUsage>
    <Description>FERRIPROX Tablets (deferiprone) contain 1,000 mg deferiprone (3-hydroxy-1,2-dimethylpyridin-4-one), a synthetic, orally active, iron-chelating agent. The molecular formula for deferiprone is C7H9NO2 and its molecular weight is 139.15 g/mol. Deferiprone has the following structural formula. Deferiprone is a white to pinkish-white powder. It is sparingly soluble in deionized water (14.3 mg/mL) and has a melting point range of 272 °C - 278 °C. FERRIPROX Tablets (twice a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “FPX” score “DR” on one side and “APO” score “1000” on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - hypromellose acetate succinate, magnesium oxide, colloidal silicon dioxide and magnesium stearate; Coating - triethyl citrate, talc, titanium dioxide, and methacrylic acid and ethyl acrylate copolymer. FERRIPROX Tablets (three times a day), 1,000 mg. White to off-white, capsule-shaped tablets, and imprinted with “APO” score “1000” on one side and plain on the other. The tablets can be broken in half along the score line. Each tablet contains 1,000 mg deferiprone and the following inactive ingredients: Tablet core - methylcellulose, crospovidone, and magnesium stearate; Coating - hypromellose, hydroxypropyl cellulose, macrogol, and titanium dioxide.</Description>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>61626-0104-4</NDCCode><ProprietaryName>Water</ProprietaryName><NonProprietaryName>Aconitum Nap, Arsenicum Alb, Borax, Calc Phos, Gelsenium, Lycopodium, Phosphoricum Ac, Picricum Ac, Plumb Met, Solidago</NonProprietaryName></NDC><NDC><NDCCode>61626-0098-4</NDCCode><ProprietaryName>Flu Immune</ProprietaryName><NonProprietaryName>Anas Barbarie Hepatis Et Cordis Extractum</NonProprietaryName></NDC><NDC><NDCCode>61626-0099-4</NDCCode><ProprietaryName>Pain Relief</ProprietaryName><NonProprietaryName>Arnica, Chamomilla, Hypericum, Ignatia, Symphytum</NonProprietaryName></NDC><NDC><NDCCode>61626-0100-4</NDCCode><ProprietaryName>Day And Night Vitals</ProprietaryName><NonProprietaryName>Allium Sat, Aloe, Arsenicum Alb, Berber Vulg, Calc Phos, Ceanothus, Chelidonium Maj, Cholesterinum, Clematis Erecta, Condurango, Gambogia, Hamamelis, Kali Brom, Kali Phos, Lycopodium, Nat Carb, Passiflora, Senna, Silicea, Solidago, Spigelia Anth, Spongia, Veratrum Vir</NonProprietaryName></NDC><NDC><NDCCode>61626-0101-4</NDCCode><ProprietaryName>Yin-yang Balance</ProprietaryName><NonProprietaryName>Adamas, Agaricus Musc, Agnus, Aletris, Angelica Sin, Arg Nit, Arnica, Avena, Baryta, Graphites, Kali Brom, Kreosotum, Lycopodium, Ocimum Sanc, Phosphoricum Ac, Selenium, Sepia, Thuja Occ.</NonProprietaryName></NDC><NDC><NDCCode>61626-0102-4</NDCCode><ProprietaryName>Earth</ProprietaryName><NonProprietaryName>Aur Met, Arg Nit, Causticum, Cinchona, Condurango, Ceanothus, Euphrasia, Fucus, Gallicum Ac, Iris Vers, Net Carb, Nitricum Ac, Phosphorus.</NonProprietaryName></NDC><NDC><NDCCode>61626-0103-4</NDCCode><ProprietaryName>Metal</ProprietaryName><NonProprietaryName>Aluminia, Ammon Carb, Anacardium, Antimon Crud, Hydrastis, Ignatia, Mag Phos, Nat Mur, Nitricum Ac, Osmium, Paraffinum, Senna, Silicea, Spongia</NonProprietaryName></NDC><NDC><NDCCode>61626-0105-4</NDCCode><ProprietaryName>Wood</ProprietaryName><NonProprietaryName>Belladonna, Berber Vulg, Carduus Mar, Chelidonium Maj, Cholesterinum, Colocynthis, Kali Carb, Nat Phos, Nitricum Ac, Nux Vom, Platinum Met, Sepia</NonProprietaryName></NDC><NDC><NDCCode>61626-0106-4</NDCCode><ProprietaryName>Fire</ProprietaryName><NonProprietaryName>Apil Mel, Baptisia, Baryta Carb, Hamamelis, Kali Brom, Kali Phos, Lachesis, Lilium, Petroleum, Phosphoricum Ac, Spigelia Anth, Sulphur, Veratrum Vir</NonProprietaryName></NDC><NDC><NDCCode>61626-0107-4</NDCCode><ProprietaryName>Para Solve</ProprietaryName><NonProprietaryName>Calc Carb, Chenopodium Anth, Cina, Croton, Filix Mas, Gambocia, Granatum, Lycopodium, Merc Corros, Nat Phos, Santoninum, Senna, Spigelia Anth, Stannum Met, Tanacetum, Teuricum Mar, Zingiber</NonProprietaryName></NDC><NDC><NDCCode>61626-0108-4</NDCCode><ProprietaryName>Flora Plus</ProprietaryName><NonProprietaryName>Aloe, Alumina, Antimon Crud, Arg Nit, Chelidonium Maj, Gambogia, Graphites, Hydrastis, Lycopodium, Silicea</NonProprietaryName></NDC><NDC><NDCCode>61626-0109-4</NDCCode><ProprietaryName>Allergy</ProprietaryName><NonProprietaryName>Allium Sat, Anacardium, Apis Mel, Gambogia, Merc Solub, Nat Carb, Nitricum Ac, Nux Vom, Phosphorus, Pulsatilla, Sulphur</NonProprietaryName></NDC><NDC><NDCCode>61626-0110-4</NDCCode><ProprietaryName>Er 911</ProprietaryName><NonProprietaryName>Aconitum Nap, Apis Mel, Arnica, Arsenicum Alb, Belladonna, Bellis, Bryonia, Calendula, Chamomilla, Cistus Canadensis, Clematis Erecta, Ferrum Phos, Histaminum, Hypericum, Ignatia, Impatiens Glan Flos, Ornithogalum, Passiflora, Phosphorus, Prunus Cerasifera, Rhus Tox, Sulphur, Symphytum, Vertarum Alb</NonProprietaryName></NDC><NDC><NDCCode>61626-0111-4</NDCCode><ProprietaryName>Scars-adhesions</ProprietaryName><NonProprietaryName>Calc Fluor, Causticum, Graphites, Hydrofluoricum Ac, Lachesis, Plumb Met, Rhus Tox, Sepia, Silicea, Thiosinaminum</NonProprietaryName></NDC><NDC><NDCCode>61626-0112-4</NDCCode><ProprietaryName>Visceral Polarity</ProprietaryName><NonProprietaryName>Aconitum Nap, Arg Nit, Chininum Pur, Echinacea Purp, Plum Met, Sepia, Sulphuricum Ac</NonProprietaryName></NDC><NDC><NDCCode>11523-0104-4</NDCCode><ProprietaryName>Claritin</ProprietaryName><NonProprietaryName>Loratadine</NonProprietaryName></NDC><NDC><NDCCode>13630-0104-4</NDCCode><ProprietaryName>Miami Beach</ProprietaryName><NonProprietaryName>Avobenzone, Homosalate, Octisalate, And Octocrylene</NonProprietaryName></NDC><NDC><NDCCode>15631-0104-4</NDCCode><ProprietaryName>Cantharidinum</ProprietaryName><NonProprietaryName>Cantharidinum</NonProprietaryName></NDC><NDC><NDCCode>37662-0104-4</NDCCode><ProprietaryName>Calcarea Nitrica</ProprietaryName><NonProprietaryName>Calcarea Nitrica</NonProprietaryName></NDC><NDC><NDCCode>38779-0104-4</NDCCode><NonProprietaryName>Methadone Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>49288-0104-4</NDCCode><ProprietaryName>Carrot</ProprietaryName><NonProprietaryName>Carrot</NonProprietaryName></NDC><NDC><NDCCode>51552-0104-4</NDCCode><NonProprietaryName>Testosterone Cypionate</NonProprietaryName></NDC><NDC><NDCCode>51754-0104-7</NDCCode><ProprietaryName>Acetylcysteine</ProprietaryName><NonProprietaryName>Acetylcysteine Injection</NonProprietaryName></NDC><NDC><NDCCode>58232-0104-4</NDCCode><ProprietaryName>Aveeno Baby Daily Moisture</ProprietaryName><NonProprietaryName>Dimethicone</NonProprietaryName></NDC><NDC><NDCCode>58443-0104-4</NDCCode><ProprietaryName>Solmate</ProprietaryName><NonProprietaryName>Avobenzone, Octisalate, Octocrylene, And Oxybenzone</NonProprietaryName></NDC><NDC><NDCCode>65096-0104-4</NDCCode><NonProprietaryName>Pioglitazone Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>71335-0104-4</NDCCode><ProprietaryName>Hydrocodone Bitartrate And Ibuprofen</ProprietaryName><NonProprietaryName>Hydrocodone Bitartrate And Ibuprofen</NonProprietaryName></NDC><NDC><NDCCode>0009-0104-04</NDCCode><ProprietaryName>Lincocin</ProprietaryName><NonProprietaryName>Lincomycin Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>10122-104-01</NDCCode><ProprietaryName>Ferriprox</ProprietaryName><NonProprietaryName>Deferiprone</NonProprietaryName></NDC><NDC><NDCCode>10122-104-05</NDCCode><ProprietaryName>Ferriprox</ProprietaryName><NonProprietaryName>Deferiprone</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",
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      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

                
{
  "NPI": [
    {
      "NPI": "1083349906",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "STAFFORD",
      "FirstName": "KADY",
      "NamePrefix": "MS.",
      "Credential": "LPC",
      "FirstLineMailingAddress": "13574 SW HIGHWAY 126",
      "MailingAddressCityName": "POWELL BUTTE",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97753-1541",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-480-6360",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-203-0307",
      "EnumerationDate": "07/24/2022",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional Counselor",
      "LicenseNumber1": "LPC6225",
      "LicenseNumberStateCode1": "ID",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C9084",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1215724679",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "SCHAY",
      "FirstName": "ANGELICA",
      "MiddleName": "NICOLE",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1841",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1841",
      "EnumerationDate": "04/21/2025",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101Y00000X",
      "Taxonomy1": "Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101Y00000X",
      "PrimaryTaxonomy": "Counselor"
    },
    {
      "NPI": "1013556505",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "IVENS",
      "FirstName": "KRYSTA",
      "FirstLineMailingAddress": "743 NW QUINCE AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-1250",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "360-526-1448",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "971-217-6150",
      "EnumerationDate": "12/31/2019",
      "LastUpdateDate": "02/15/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C7963",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "02/15/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1497336275",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "ARANT",
      "FirstName": "ERIN",
      "MiddleName": "HENNESSEY",
      "FirstLineMailingAddress": "4639 SW 37TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-6776",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "04/14/2021",
      "LastUpdateDate": "04/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "225X00000X",
      "Taxonomy1": "Occupational Therapist",
      "LicenseNumber1": "390047",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/14/2021",
      "PrimaryTaxonomyCode": "225X00000X",
      "PrimaryTaxonomy": "Occupational Therapist"
    },
    {
      "NPI": "1174191407",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "GRIMALT",
      "FirstName": "EUGENIA",
      "MiddleName": "N",
      "Credential": "PT",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1848",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "06/14/2021",
      "LastUpdateDate": "06/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "2251P0200X",
      "Taxonomy1": "Pediatric Physical Therapist",
      "LicenseNumber1": "63979",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization.",
      "CertificationDate": "06/14/2021",
      "PrimaryTaxonomyCode": "2251P0200X",
      "PrimaryTaxonomy": "Pediatric Physical Therapist"
    },
    {
      "NPI": "1912604117",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "PAINTER",
      "FirstName": "JENNIFER",
      "FirstLineMailingAddress": "20080 DOANNA WAY UNIT 3",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97702-2931",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "209-743-9813",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "02/08/2023",
      "LastUpdateDate": "02/08/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "02/08/2023",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1396434700",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "GROVE",
      "FirstName": "JENNIFER",
      "MiddleName": "RHEA",
      "FirstLineMailingAddress": "303 NW BROADWAY ST",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97703-2658",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "801-573-6047",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "801-573-6047",
      "EnumerationDate": "05/02/2023",
      "LastUpdateDate": "05/02/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "1041C0700X",
      "Taxonomy1": "Clinical Social Worker",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "05/02/2023",
      "PrimaryTaxonomyCode": "1041C0700X",
      "PrimaryTaxonomy": "Clinical Social Worker"
    },
    {
      "NPI": "1407698970",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "REDDEN",
      "FirstName": "SHANNON",
      "Credential": "CHW",
      "OtherLastName": "MCDOUGALL",
      "OtherFirstName": "SHANNON",
      "OtherLastNameTypeCode": "1",
      "FirstLineMailingAddress": "2312 NE 5TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-8488",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-460-2192",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "PracticeLocationAddressFaxNumber": "541-550-7956",
      "EnumerationDate": "06/06/2024",
      "LastUpdateDate": "06/06/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "172V00000X",
      "Taxonomy1": "Community Health Worker",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "06/06/2024",
      "PrimaryTaxonomyCode": "172V00000X",
      "PrimaryTaxonomy": "Community Health Worker"
    },
    {
      "NPI": "1942022256",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "JACQUOT",
      "FirstName": "SHAYLA",
      "FirstLineMailingAddress": "PO BOX 1397",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97709-1397",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1848",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "10/28/2024",
      "LastUpdateDate": "10/28/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "10/26/2024",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1912723131",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "WEIMER",
      "FirstName": "ALAYNA",
      "FirstLineMailingAddress": "2748 NW 19TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-7766",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-499-8292",
      "EnumerationDate": "12/03/2024",
      "LastUpdateDate": "12/03/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "171M00000X",
      "Taxonomy1": "Case Manager/Care Coordinator",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "12/03/2024",
      "PrimaryTaxonomyCode": "171M00000X",
      "PrimaryTaxonomy": "Case Manager/Care Coordinator"
    },
    {
      "NPI": "1790594125",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "WIDDER",
      "FirstName": "JENNIFER",
      "MiddleName": "LYNN",
      "FirstLineMailingAddress": "22350 CALGARY DR",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97702-9216",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-749-8895",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1858",
      "EnumerationDate": "12/31/2024",
      "LastUpdateDate": "12/31/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "175T00000X",
      "Taxonomy1": "Peer Specialist",
      "LicenseNumber1": "112910",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "12/31/2024",
      "PrimaryTaxonomyCode": "175T00000X",
      "PrimaryTaxonomy": "Peer Specialist"
    },
    {
      "NPI": "1538965306",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "PARSONS",
      "FirstName": "JEANINE",
      "MiddleName": "JEWELL",
      "FirstLineMailingAddress": "2821 SW 28TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-8681",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "760-927-4761",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "02/21/2025",
      "LastUpdateDate": "02/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "175T00000X",
      "Taxonomy1": "Peer Specialist",
      "LicenseNumber1": "113398",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "02/21/2025",
      "PrimaryTaxonomyCode": "175T00000X",
      "PrimaryTaxonomy": "Peer Specialist"
    }
  ]
}
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