RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (42 ms elapsed)

{
  "NDC": [
    {
      "NDCCode": "82797-128-12",
      "PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (82797-128-12) ",
      "NDC11Code": "82797-0128-12",
      "ProductNDC": "82797-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Menola Tonic",
      "NonProprietaryName": "Moringa Olifera, Avena Sativa, Ginseng, Acidum Lacticum, Nicotinamide, Thiamine Hydrochloride, Riboflavin",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240702",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "AMERICAN GINSENG; AVENA SATIVA WHOLE; LACTIC ACID; MORINGA OLEIFERA LEAF; NIACINAMIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE",
      "StrengthNumber": ".18; 4.8; .54; 2.4; .09; .48; .09",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Pharm_Classes": "Acidifying Activity [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240702",
      "SamplePackage": "N",
      "IndicationAndUsage": "Menola tonic is for male sexual debility and general weakness. Effective in anemic conditions and lowered disease resistance. Acts as a tonic for nervous exhaustion. Also advised during convalescence."
    },
    {
      "NDCCode": "82797-123-12",
      "PackageDescription": "1 BOTTLE in 1 BOX (82797-123-12)  / 120 mL in 1 BOTTLE (82797-123-11) ",
      "NDC11Code": "82797-0123-12",
      "ProductNDC": "82797-123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Masood Ivypan Cough Syrup",
      "NonProprietaryName": "Hedera Helix",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20221201",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "HEDERA HELIX LEAF",
      "StrengthNumber": "9.6",
      "StrengthUnit": "mg/120mL",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20221201",
      "SamplePackage": "N",
      "IndicationAndUsage": "Uses. For the temporary relief of. : 1 Cough with Sputum and Sinus congestion."
    },
    {
      "NDCCode": "82797-125-12",
      "PackageDescription": "120 mL in 1 BOTTLE (82797-125-12) ",
      "NDC11Code": "82797-0125-12",
      "ProductNDC": "82797-125",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "K Flush",
      "NonProprietaryName": "Belladonna, Berberls Vulgarls, Cantharis, , Hydrangea, Parelra Brava, Rubla Tinct, Solidago, Sarsaparilla, Urtica Urens",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240404",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "BELLADONNA LEAF; BERBERIS VULGARIS FRUIT; HYDRANGEA ARBORESCENS BARK; LYTTA VESICATORIA; RUBIA CORDIFOLIA ROOT; SARSAPARILLA; SOLIDAGO CANADENSIS FLOWERING TOP; URTICA URENS FLOWER",
      "StrengthNumber": ".12; 1.7; .492; .492; .24; .24; .24; .24",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240404",
      "SamplePackage": "N",
      "IndicationAndUsage": "It is indicated for removal of kidney, ureter and bladder stones as well as related infection, inflammation and burning sensation during urination."
    },
    {
      "NDCCode": "82797-127-12",
      "PackageDescription": "120 mL in 1 BOTTLE (82797-127-12) ",
      "NDC11Code": "82797-0127-12",
      "ProductNDC": "82797-127",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Alfalfa Tonic",
      "NonProprietaryName": "Alfalfa, China Off, Avena Sativa, Hydrastis Can, Calc Phos, Kali Phos, Nat Phos, Mag Phos, Ferr Phos, Ferric Citrate, Acidum Phos",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240516",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "ALFALFA; AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; CINCHONA BARK; DIBASIC POTASSIUM PHOSPHATE; FERRIC CITRATE ANHYDROUS; FERROUS PHOSPHATE; HYDRASTIS CANADENSIS WHOLE; MAGNESIUM PHOSPHATE, DIBASIC; PHOSPHORIC ACID; SODIUM PHOSPHATE",
      "StrengthNumber": "4.2; 2.4; .48; 3; .48; 3; .48; 1.44; .48; .36; .48",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Pharm_Classes": "Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Osmotic Activity [MoA], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240516",
      "SamplePackage": "N",
      "IndicationAndUsage": "Indications and Usage. Convalescence, General weakness, Nervous debility, loss of appetite, anemia, and chlorosis."
    },
    {
      "NDCCode": "82797-129-12",
      "PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (82797-129-12) ",
      "NDC11Code": "82797-0129-12",
      "ProductNDC": "82797-129",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Alfalfa Plus Ginseng Syrup",
      "NonProprietaryName": "Alfalfa, China Off, Avena Sativa, Hydrastis Can, Ginseng, Ferric Citrate, Nat Phos, Mag Phos, Calc Phos, Kali Phos, Ferr Phos,",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240704",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "ALFALFA; AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; CINCHONA OFFICINALIS WHOLE; DIBASIC POTASSIUM PHOSPHATE; FERRIC CITRATE ANHYDROUS; FERROUS SULFATE; HYDRASTIS CANADENSIS WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PANAX GINSENG WHOLE; SODIUM PHOSPHATE",
      "StrengthNumber": "4.32; 2.4; .48; 3.84; .48; 3; .48; 1.44; .48; 2.16; .48",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Pharm_Classes": "Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240704",
      "SamplePackage": "N",
      "IndicationAndUsage": "Convalescence, General weakness, Nervous debility, loss of appetite, boost immunity, anemia and chlorosis. Improves appetite and helps in digestion resulting in improved mental and physical health and weight gain."
    },
    {
      "NDCCode": "82797-130-12",
      "PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (82797-130-12) ",
      "NDC11Code": "82797-0130-12",
      "ProductNDC": "82797-130",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Androtone Syrup",
      "NonProprietaryName": "Tribulus Terr, Avena Sativa,sterculia Acum, Nuphar Lut, Sabal Serr, Agnus Cast, Lycopodium Clav, Gentiana Lut, Yohimbinum, Lecithin, Natrum Phos, Kali Phos, Calcarea Phos, Natrum Mur, Strychninum Sulph, Acidum Phos, Choloformum",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240708",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; COLA ACUMINATA WHOLE; GENTIANA LUTEA WHOLE; LECITHIN, SOYBEAN; LYCOPODIUM CLAVATUM WHOLE; MONOBASIC POTASSIUM PHOSPHATE; NUPHAR LUTEA WHOLE; PHOSPHORIC ACID; SABAL PALMETTO WHOLE; SODIUM CHLORIDE; SODIUM PHOSPHATE; STRYCHNINE; TRIBULUS TERRESTRIS WHOLE; VITEX AGNUS-CASTUS WHOLE; YOHIMBINE",
      "StrengthNumber": ".08; .005; .03; .01; .0625; .01; .005; .03; .01; .03; .005; .005; .015; .08; .02; .01",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Pharm_Classes": "Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240708",
      "SamplePackage": "N",
      "IndicationAndUsage": "Indicated in loss of sex drive and erectile dysfunction. Helpful for those who want to build their muscles. Also increases testosterone levels in the bloodstream."
    },
    {
      "NDCCode": "82797-131-01",
      "PackageDescription": "1 BOTTLE in 1 BOX (82797-131-01)  / 120 mL in 1 BOTTLE (82797-131-12) ",
      "NDC11Code": "82797-0131-01",
      "ProductNDC": "82797-131",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Nefritol Syrup",
      "NonProprietaryName": "Berberis Vulgaris 8x, Epigea Repens, Apis Mellifica 6, Hydrangea Arborescens , Cantharis 30 , Pareira Brava 3, Lycopodium Clav , Solidago Virgaurea",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20250422",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "CHONDRODENDRON TOMENTOSUM ROOT; HYDRANGEA ARBORESCENS WHOLE; EPIGAEA REPENS; APIS MELLIFERA; BERBERIS VULGARIS WHOLE; LYTTA VESICATORIA; SOLIDAGO VIRGAUREA WHOLE; LYCOPODIUM CLAVATUM WHOLE",
      "StrengthNumber": ".0027; .0075; .0027; .0075; .0075; .005; .0027; .0025",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "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": "Deprecated",
      "LastUpdate": "2026-08-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20250422",
      "SamplePackage": "N",
      "IndicationAndUsage": "it is indicated for the supportive treatment of conditions related to urinary tract including its infections, pain and inflammation."
    },
    {
      "NDCCode": "82797-132-01",
      "PackageDescription": "1 BOTTLE in 1 BOX (82797-132-01)  / 120 mL in 1 BOTTLE (82797-132-12) ",
      "NDC11Code": "82797-0132-01",
      "ProductNDC": "82797-132",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Vitmin C",
      "NonProprietaryName": "Acid Phos D3, Cocculus D5, Helonias Dioca D5, Zincum Met D6, Citrus Limonum , Rosa Canina , Ascorbic Acid, Citric Acid",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20250424",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "ROSA CANINA WHOLE; ZINC; ASCORBIC ACID; STRYCHNOS IGNATII WHOLE; CITRUS LIMON WHOLE; CHAMAELIRIUM LUTEUM WHOLE; ANAMIRTA COCCULUS WHOLE; PHOSPHORIC ACID",
      "StrengthNumber": ".01; 7.5; .01; .003; .01; .01; .01; .01",
      "StrengthUnit": "mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL",
      "Pharm_Classes": "Ascorbic Acid [CS], Vitamin C [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2026-08-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20250424",
      "SamplePackage": "N",
      "IndicationAndUsage": "Conditions of Nervous Exhaustion. General Neurasthenia. Insomnia. Fatigue. Lack of Energy. Inability to concentrate."
    },
    {
      "NDCCode": "82797-333-12",
      "PackageDescription": "30 g in 1 BOTTLE, GLASS (82797-333-12) ",
      "NDC11Code": "82797-0333-12",
      "ProductNDC": "82797-333",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Masood Abrotanum",
      "NonProprietaryName": "Abrotanum",
      "DosageFormName": "PELLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20230201",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "ARTEMISIA ABROTANUM FLOWERING TOP",
      "StrengthNumber": "1",
      "StrengthUnit": "g/30g",
      "Status": "Deprecated",
      "LastUpdate": "2025-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20230201",
      "SamplePackage": "N",
      "IndicationAndUsage": "To be used for acute, self-limiting conditions according to standard homeopathic indications."
    },
    {
      "NDCCode": "33342-128-12",
      "PackageDescription": "10 BLISTER PACK in 1 CARTON (33342-128-12)  > 10 TABLET in 1 BLISTER PACK",
      "NDC11Code": "33342-0128-12",
      "ProductNDC": "33342-128",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Telmisartan And Hydrochlorothiazide",
      "NonProprietaryName": "Telmisartan And Hydrochlorothiazide",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151102",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA204169",
      "LabelerName": "Macleods Pharmaceuticals Limited",
      "SubstanceName": "TELMISARTAN; HYDROCHLOROTHIAZIDE",
      "StrengthNumber": "40; 12.5",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2020-09-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20151102",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "42939-128-12",
      "PackageDescription": "3785 mL in 1 BOTTLE, PLASTIC (42939-128-12) ",
      "NDC11Code": "42939-0128-12",
      "ProductNDC": "42939-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Scrub, Scrub-stat, Foam Safe, Micro-guard",
      "NonProprietaryName": "Chlorhexidine Gluconate",
      "DosageFormName": "SOLUTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "19860722",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA019258",
      "LabelerName": "AVA, Inc.",
      "SubstanceName": "CHLORHEXIDINE GLUCONATE",
      "StrengthNumber": "40",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Decreased Cell Wall Integrity [PE]",
      "Status": "Active",
      "LastUpdate": "2024-05-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "19860722",
      "SamplePackage": "N",
      "IndicationAndUsage": "surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care . healthcare personnel handwash: handwash to help reduce bacteria that potentially can cause disease . skin wound and general cleanser: helps reduce bacteria on the skin ."
    },
    {
      "NDCCode": "46063-552-12",
      "PackageDescription": "128 g in 1 CAN (46063-552-12) ",
      "NDC11Code": "46063-0552-12",
      "ProductNDC": "46063-552",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Relispray Antifungal Powder",
      "NonProprietaryName": "Miconazole Nitrate",
      "DosageFormName": "AEROSOL, SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20220301",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M005",
      "LabelerName": "Midas-Care Pharmaceuticals Pvt. Ltd.",
      "SubstanceName": "MICONAZOLE NITRATE",
      "StrengthNumber": ".02",
      "StrengthUnit": "g/g",
      "Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20220301",
      "SamplePackage": "N",
      "IndicationAndUsage": "effectively treats most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). relieves itching, scaling, burning and discomfort which may accompany these conditions."
    },
    {
      "NDCCode": "46063-810-12",
      "PackageDescription": "128 g in 1 CAN (46063-810-12) ",
      "NDC11Code": "46063-0810-12",
      "ProductNDC": "46063-810",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Relispray Antifungal Liquid",
      "NonProprietaryName": "Tolnaftate",
      "DosageFormName": "AEROSOL, SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20220301",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M005",
      "LabelerName": "Midas-Care Pharmaceuticals Pvt. Ltd.",
      "SubstanceName": "TOLNAFTATE",
      "StrengthNumber": ".01",
      "StrengthUnit": "g/g",
      "Status": "Active",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220301",
      "SamplePackage": "N",
      "IndicationAndUsage": "effectively treats most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). relieves itching, scaling, burning and discomfort which may accompany these conditions."
    },
    {
      "NDCCode": "49348-128-12",
      "PackageDescription": "1 BOTTLE in 1 CARTON (49348-128-12)  > 60 TABLET, FILM COATED in 1 BOTTLE",
      "NDC11Code": "49348-0128-12",
      "ProductNDC": "49348-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunmark Acid Reducer",
      "NonProprietaryName": "Famotidine",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20090910",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA075400",
      "LabelerName": "Strategic Sourcing Services LLC",
      "SubstanceName": "FAMOTIDINE",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20090910",
      "SamplePackage": "N",
      "IndicationAndUsage": "relieves heartburn associated with acid indigestion and sour stomach. prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages."
    },
    {
      "NDCCode": "50804-128-02",
      "PackageDescription": "2 BLISTER PACK in 1 CARTON (50804-128-02)  / 12 TABLET, COATED in 1 BLISTER PACK",
      "NDC11Code": "50804-0128-02",
      "ProductNDC": "50804-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Allergy Multi Symptom",
      "NonProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20200801",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M012",
      "LabelerName": "GOODSENSE",
      "SubstanceName": "ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 2; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]",
      "Status": "Active",
      "LastUpdate": "2024-10-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20200801",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily relieves these symptoms of hay fever or other upper respiratory allergies: headachenasal congestionsinus congestion and pressureminor aches and painsrunny nose and sneezing. helps clear nasal passages. helps decongest sinus openings and passages. temporarily relieves these additional symptoms of hay fever:  itching of the nose or throatitchy, watery eyes."
    },
    {
      "NDCCode": "57344-128-02",
      "PackageDescription": "2 BLISTER PACK in 1 CARTON (57344-128-02)  > 12 TABLET, COATED in 1 BLISTER PACK",
      "NDC11Code": "57344-0128-02",
      "ProductNDC": "57344-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride",
      "NonProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20120802",
      "EndMarketingDate": "20220630",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part341",
      "LabelerName": "AAA Pharmaceutical, Inc.",
      "SubstanceName": "ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 2; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2022-07-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20120802",
      "EndMarketingDatePackage": "20220630",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "57344-128-06",
      "PackageDescription": "4 BLISTER PACK in 1 CARTON (57344-128-06)  > 12 TABLET, COATED in 1 BLISTER PACK",
      "NDC11Code": "57344-0128-06",
      "ProductNDC": "57344-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride",
      "NonProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20121228",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part341",
      "LabelerName": "AAA Pharmaceutical, Inc.",
      "SubstanceName": "ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 2; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-10-17",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20121228",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "58159-128-12",
      "PackageDescription": ".001 kg in 1 DRUM (58159-128-12) ",
      "NDC11Code": "58159-0128-12",
      "ProductNDC": "58159-128",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Eltrombopag Choline",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20250724",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "NURAY CHEMICALS PRIVATE LIMITED",
      "SubstanceName": "ELTROMBOPAG CHOLINE",
      "StrengthNumber": "35",
      "StrengthUnit": "kg/35kg",
      "Status": "Unfinished",
      "LastUpdate": "2025-08-05",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "24-JUL-25"
    },
    {
      "NDCCode": "58411-128-30",
      "PackageDescription": "1 TRAY in 1 CARTON (58411-128-30)  > 12 g in 1 TRAY",
      "NDC11Code": "58411-0128-30",
      "ProductNDC": "58411-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Shiseido Uv Protective Compact (refill)",
      "ProprietaryNameSuffix": "Dark Beige",
      "NonProprietaryName": "Octinoxate, Octocrylene, And Titanium Dioxide",
      "DosageFormName": "POWDER",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20140201",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "SHISEIDO AMERICAS CORPORATION",
      "SubstanceName": "OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE",
      "StrengthNumber": "888; 600; 1416",
      "StrengthUnit": "mg/12g; mg/12g; mg/12g",
      "Status": "Deprecated",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20140201",
      "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": "63187-128-12",
      "PackageDescription": "12 TABLET, FILM COATED in 1 BOTTLE (63187-128-12) ",
      "NDC11Code": "63187-0128-12",
      "ProductNDC": "63187-128",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Ketorolac Tromethamine",
      "NonProprietaryName": "Ketorolac Tromethamine",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "19980617",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA074754",
      "LabelerName": "Proficient Rx LP",
      "SubstanceName": "KETOROLAC TROMETHAMINE",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitor [EPC], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]",
      "Status": "Active",
      "LastUpdate": "2022-04-12",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220208",
      "SamplePackage": "N",
      "IndicationAndUsage": "Carefully consider the potential benefits and risks of Ketorolac Tromethamine Tablets USP and other treatment options before deciding to use Ketorolac Tromethamine Tablets USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.",
      "Description": "Ketorolac Tromethamine Tablets USP are a member of the pyrrolo-pyrrole group of non-steroidal anti-inflammatory drugs (NSAIDs). The chemical name for ketorolac tromethamine, USP is (±)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid, compound with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1). The structural formula is. C15H13NO3 .C4H11NO3 M.W. 376.40. Ketorolac tromethamine, USP is a racemic mixture of [-]S and [+]R ketorolac tromethamine, USP. Ketorolac tromethamine, USP may exist in three crystal forms. All forms are equally soluble in water. Ketorolac tromethamine, USP has a pKa of 3.5 and an n-octanol/water partition coefficient of 0.26. Ketorolac Tromethamine Tablets USP are white, round, convex, unscored, film coated tablets. Each tablet, for oral administration, contains 10 mg ketorolac tromethamine, USP, the active ingredient. In addition, each tablet contains the following inactive ingredients: hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, and titanium dioxide."
    },
    {
      "NDCCode": "68998-128-02",
      "PackageDescription": "2 BLISTER PACK in 1 CARTON (68998-128-02)  > 12 TABLET, COATED in 1 BLISTER PACK",
      "NDC11Code": "68998-0128-02",
      "ProductNDC": "68998-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Allergy Multi-symptom",
      "NonProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20100601",
      "EndMarketingDate": "20211231",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part341",
      "LabelerName": "Marc Glassman, Inc.",
      "SubstanceName": "ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 2; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2022-01-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20100601",
      "EndMarketingDatePackage": "20211231",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "71406-128-12",
      "PackageDescription": "120 TABLET, DELAYED RELEASE in 1 BOTTLE (71406-128-12) ",
      "NDC11Code": "71406-0128-12",
      "ProductNDC": "71406-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Aspirin 81 Mg",
      "NonProprietaryName": "Aspirin Enteric Coated Tablets 81 Mg",
      "DosageFormName": "TABLET, DELAYED RELEASE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20210503",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M013",
      "LabelerName": "AACE Pharmaceuticals, Inc.",
      "SubstanceName": "ASPIRIN",
      "StrengthNumber": "81",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2025-05-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20210514",
      "SamplePackage": "Y",
      "IndicationAndUsage": "Pin Reliever."
    },
    {
      "NDCCode": "72476-128-02",
      "PackageDescription": "2 BLISTER PACK in 1 CARTON (72476-128-02)  / 12 TABLET, COATED in 1 BLISTER PACK",
      "NDC11Code": "72476-0128-02",
      "ProductNDC": "72476-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Allergy Multisymptom",
      "NonProprietaryName": "Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20201021",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M012",
      "LabelerName": "RETAIL BUSINESS SERVICES , LLC.",
      "SubstanceName": "ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 2; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]",
      "Status": "Active",
      "LastUpdate": "2024-10-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20201021",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily relieves these symptoms of hay fever or other upper respiratory allergies: headachesinus congestion and pressurenasal congestionrunny nose and sneezingminor aches and pains. temporarily relieves these additional symptoms of hay fever: itching of the nose or throatitchy, watery eyes. helps clear nasal passages. helps decongest sinus openings and passages."
    },
    {
      "NDCCode": "72520-121-12",
      "PackageDescription": "128 g in 1 TUBE (72520-121-12) ",
      "NDC11Code": "72520-0121-12",
      "ProductNDC": "72520-121",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Nuvalu Creamy Petroleum",
      "NonProprietaryName": "Petrolatum",
      "DosageFormName": "JELLY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20231101",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M016",
      "LabelerName": "JC SALES",
      "SubstanceName": "PETROLATUM",
      "StrengthNumber": "30",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20231101",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather."
    },
    {
      "NDCCode": "75603-128-12",
      "PackageDescription": "3785 mL in 1 JUG (75603-128-12) ",
      "NDC11Code": "75603-0128-12",
      "ProductNDC": "75603-128",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Hand Sanitizer",
      "NonProprietaryName": "Alcohol",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20200330",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part333A",
      "LabelerName": "BLACK BAND, LLC.",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "80",
      "StrengthUnit": "mL/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2022-01-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20200330",
      "SamplePackage": "N",
      "IndicationAndUsage": "Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available."
    },
    {
      "NDCCode": "76176-230-12",
      "PackageDescription": "128 g in 1 TUBE (76176-230-12) ",
      "NDC11Code": "76176-0230-12",
      "ProductNDC": "76176-230",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Nuvalu Creamy Petroleum",
      "NonProprietaryName": "Petrolatum",
      "DosageFormName": "JELLY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20231101",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M016",
      "LabelerName": "Ningbo Liyuan Daily Chemical Products Co.,Ltd.",
      "SubstanceName": "PETROLATUM",
      "StrengthNumber": "30",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2024-12-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20231101",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather."
    },
    {
      "NDCCode": "82797-423-30",
      "PackageDescription": "30 mg in 1 BLISTER PACK (82797-423-30) ",
      "NDC11Code": "82797-0423-30",
      "ProductNDC": "82797-423",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Enerjizer",
      "NonProprietaryName": "Avena Sativa, Alfalfa, Echinacea, Ginkgo Biloba, Ginseng Panax, Caffeinum, Gentiana Lut, Sterculia Acum, Calcium Phosphate, Chromium Oxide, Cobaltum Met, Cuprum Sulphuricum, Iodium, Lecithinum, Manganese Sulphate, Magnesium Oxide, Kali Muriaticum, Selenium, Zinc Sulphate",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240715",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Dr. Masood Homeopathic Pharmaceuticals Private Limited",
      "SubstanceName": "ALFALFA; AVENA SATIVA WHOLE; BASIC COPPER SULFATE; CAFFEINE; CALCIUM PHOSPHATE; CHROMIC OXIDE; COBALT; COLA ACUMINATA WHOLE; ECHINACEA, UNSPECIFIED; GENTIANA LUTEA WHOLE; GINKGO BILOBA WHOLE; IODINE; LECITHIN, SOYBEAN; MAGNESIUM OXIDE; MANGANESE SULFATE; PANAX GINSENG WHOLE; POTASSIUM CHLORIDE; SELENIUM; ZINC SULFATE",
      "StrengthNumber": ".11392; .11392; .00128; .192; .128; .00128; .00128; .0576; .0576; .0576; .0128; .0128; .064; .0128; .0128; .0128; .0128; .0032; .0192",
      "StrengthUnit": "mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg",
      "Pharm_Classes": "Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cell-mediated Immunity [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Methylxanthine [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Xanthines [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2026-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20240715",
      "SamplePackage": "N",
      "IndicationAndUsage": "Restores the lost vigour and vitality. Bad effects of prolonged illness. Mental fatigue or exhaustion. Acts as prophylactic against viral diseases. Lowers cholesterol and control glucose level in body. Reduce inflammation in body. Helpful in regulation of blood pressure and reduce fatigue. Keeps you energetic during exercise. Makes muscles stronger. Fulfill iodine deficiency and helpful in thyroid gland functioning. Prevents from cerebral thrombosis and stroke."
    },
    {
      "NDCCode": "0096-0741-04",
      "PackageDescription": "128 g in 1 BOTTLE (0096-0741-04) ",
      "NDC11Code": "00096-0741-04",
      "ProductNDC": "0096-0741",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Solbar Fifty Spf50",
      "NonProprietaryName": "Solbar Fifty Spf50",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "19960601",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M020",
      "LabelerName": "Person and Covey",
      "SubstanceName": "OCTOCRYLENE; OCTINOXATE; OXYBENZONE; AVOBENZONE",
      "StrengthNumber": ".1; .08; .06; .011",
      "StrengthUnit": "g/g; g/g; g/g; g/g",
      "Status": "Active",
      "LastUpdate": "2025-12-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "19960601",
      "SamplePackage": "N",
      "IndicationAndUsage": "Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun."
    },
    {
      "NDCCode": "0338-0147-03",
      "PackageDescription": "24 BAG in 1 CARTON (0338-0147-03)  > 500 mL in 1 BAG",
      "NDC11Code": "00338-0147-03",
      "ProductNDC": "0338-0147",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Plasma-lyte 56 And Dextrose",
      "NonProprietaryName": "Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "19790201",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA017385",
      "LabelerName": "Baxter Healthcare Corporation",
      "SubstanceName": "DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM ACETATE; MAGNESIUM ACETATE TETRAHYDRATE",
      "StrengthNumber": "5; 234; 128; 32",
      "StrengthUnit": "g/100mL; mg/100mL; mg/100mL; mg/100mL",
      "Pharm_Classes": "Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2015-12-18"
    },
    {
      "NDCCode": "0338-0147-04",
      "PackageDescription": "14 BAG in 1 CARTON (0338-0147-04)  > 1000 mL in 1 BAG",
      "NDC11Code": "00338-0147-04",
      "ProductNDC": "0338-0147",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Plasma-lyte 56 And Dextrose",
      "NonProprietaryName": "Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "19790201",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA017385",
      "LabelerName": "Baxter Healthcare Corporation",
      "SubstanceName": "DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM ACETATE; MAGNESIUM ACETATE TETRAHYDRATE",
      "StrengthNumber": "5; 234; 128; 32",
      "StrengthUnit": "g/100mL; mg/100mL; mg/100mL; mg/100mL",
      "Pharm_Classes": "Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2016-12-27"
    }
  ]
}
                    

{"NDC":[{"NDCCode":"82797-128-12","ProprietaryName":"Menola Tonic","NonProprietaryName":"Moringa Olifera, Avena Sativa, Ginseng, Acidum Lacticum, Nicotinamide, Thiamine Hydrochloride, Riboflavin"},{"NDCCode":"82797-123-12","ProprietaryName":"Masood Ivypan Cough Syrup","NonProprietaryName":"Hedera Helix"},{"NDCCode":"82797-125-12","ProprietaryName":"K Flush","NonProprietaryName":"Belladonna, Berberls Vulgarls, Cantharis, , Hydrangea, Parelra Brava, Rubla Tinct, Solidago, Sarsaparilla, Urtica Urens"},{"NDCCode":"82797-127-12","ProprietaryName":"Alfalfa Tonic","NonProprietaryName":"Alfalfa, China Off, Avena Sativa, Hydrastis Can, Calc Phos, Kali Phos, Nat Phos, Mag Phos, Ferr Phos, Ferric Citrate, Acidum Phos"},{"NDCCode":"82797-129-12","ProprietaryName":"Alfalfa Plus Ginseng Syrup","NonProprietaryName":"Alfalfa, China Off, Avena Sativa, Hydrastis Can, Ginseng, Ferric Citrate, Nat Phos, Mag Phos, Calc Phos, Kali Phos, Ferr Phos,"},{"NDCCode":"82797-130-12","ProprietaryName":"Androtone Syrup","NonProprietaryName":"Tribulus Terr, Avena Sativa,sterculia Acum, Nuphar Lut, Sabal Serr, Agnus Cast, Lycopodium Clav, Gentiana Lut, Yohimbinum, Lecithin, Natrum Phos, Kali Phos, Calcarea Phos, Natrum Mur, Strychninum Sulph, Acidum Phos, Choloformum"},{"NDCCode":"82797-131-01","ProprietaryName":"Nefritol Syrup","NonProprietaryName":"Berberis Vulgaris 8x, Epigea Repens, Apis Mellifica 6, Hydrangea Arborescens , Cantharis 30 , Pareira Brava 3, Lycopodium Clav , Solidago Virgaurea"},{"NDCCode":"82797-132-01","ProprietaryName":"Vitmin C","NonProprietaryName":"Acid Phos D3, Cocculus D5, Helonias Dioca D5, Zincum Met D6, Citrus Limonum , Rosa Canina , Ascorbic Acid, Citric Acid"},{"NDCCode":"82797-333-12","ProprietaryName":"Masood Abrotanum","NonProprietaryName":"Abrotanum"},{"NDCCode":"33342-128-12","ProprietaryName":"Telmisartan And Hydrochlorothiazide","NonProprietaryName":"Telmisartan And Hydrochlorothiazide"},{"NDCCode":"42939-128-12","ProprietaryName":"Scrub, Scrub-stat, Foam Safe, Micro-guard","NonProprietaryName":"Chlorhexidine Gluconate"},{"NDCCode":"46063-552-12","ProprietaryName":"Relispray Antifungal Powder","NonProprietaryName":"Miconazole Nitrate"},{"NDCCode":"46063-810-12","ProprietaryName":"Relispray Antifungal Liquid","NonProprietaryName":"Tolnaftate"},{"NDCCode":"49348-128-12","ProprietaryName":"Sunmark Acid Reducer","NonProprietaryName":"Famotidine"},{"NDCCode":"50804-128-02","ProprietaryName":"Allergy Multi Symptom","NonProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride"},{"NDCCode":"57344-128-02","ProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride","NonProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride"},{"NDCCode":"57344-128-06","ProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride","NonProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride"},{"NDCCode":"58159-128-12","NonProprietaryName":"Eltrombopag Choline"},{"NDCCode":"58411-128-30","ProprietaryName":"Shiseido Uv Protective Compact (refill)","NonProprietaryName":"Octinoxate, Octocrylene, And Titanium Dioxide"},{"NDCCode":"63187-128-12","ProprietaryName":"Ketorolac Tromethamine","NonProprietaryName":"Ketorolac Tromethamine"},{"NDCCode":"68998-128-02","ProprietaryName":"Allergy Multi-symptom","NonProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride"},{"NDCCode":"71406-128-12","ProprietaryName":"Aspirin 81 Mg","NonProprietaryName":"Aspirin Enteric Coated Tablets 81 Mg"},{"NDCCode":"72476-128-02","ProprietaryName":"Allergy Multisymptom","NonProprietaryName":"Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride"},{"NDCCode":"72520-121-12","ProprietaryName":"Nuvalu Creamy Petroleum","NonProprietaryName":"Petrolatum"},{"NDCCode":"75603-128-12","ProprietaryName":"Hand Sanitizer","NonProprietaryName":"Alcohol"},{"NDCCode":"76176-230-12","ProprietaryName":"Nuvalu Creamy Petroleum","NonProprietaryName":"Petrolatum"},{"NDCCode":"82797-423-30","ProprietaryName":"Enerjizer","NonProprietaryName":"Avena Sativa, Alfalfa, Echinacea, Ginkgo Biloba, Ginseng Panax, Caffeinum, Gentiana Lut, Sterculia Acum, Calcium Phosphate, Chromium Oxide, Cobaltum Met, Cuprum Sulphuricum, Iodium, Lecithinum, Manganese Sulphate, Magnesium Oxide, Kali Muriaticum, Selenium, Zinc Sulphate"},{"NDCCode":"0096-0741-04","ProprietaryName":"Solbar Fifty Spf50","NonProprietaryName":"Solbar Fifty Spf50"},{"NDCCode":"0338-0147-03","ProprietaryName":"Plasma-lyte 56 And Dextrose","NonProprietaryName":"Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate"},{"NDCCode":"0338-0147-04","ProprietaryName":"Plasma-lyte 56 And Dextrose","NonProprietaryName":"Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate"}]}
                    

<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <NDC>
    <NDCCode>82797-128-12</NDCCode>
    <PackageDescription>120 mL in 1 BOTTLE, PLASTIC (82797-128-12) </PackageDescription>
    <NDC11Code>82797-0128-12</NDC11Code>
    <ProductNDC>82797-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Menola Tonic</ProprietaryName>
    <NonProprietaryName>Moringa Olifera, Avena Sativa, Ginseng, Acidum Lacticum, Nicotinamide, Thiamine Hydrochloride, Riboflavin</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240702</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>AMERICAN GINSENG; AVENA SATIVA WHOLE; LACTIC ACID; MORINGA OLEIFERA LEAF; NIACINAMIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>.18; 4.8; .54; 2.4; .09; .48; .09</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Pharm_Classes>Acidifying Activity [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240702</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Menola tonic is for male sexual debility and general weakness. Effective in anemic conditions and lowered disease resistance. Acts as a tonic for nervous exhaustion. Also advised during convalescence.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-123-12</NDCCode>
    <PackageDescription>1 BOTTLE in 1 BOX (82797-123-12)  / 120 mL in 1 BOTTLE (82797-123-11) </PackageDescription>
    <NDC11Code>82797-0123-12</NDC11Code>
    <ProductNDC>82797-123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Masood Ivypan Cough Syrup</ProprietaryName>
    <NonProprietaryName>Hedera Helix</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20221201</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>HEDERA HELIX LEAF</SubstanceName>
    <StrengthNumber>9.6</StrengthNumber>
    <StrengthUnit>mg/120mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20221201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Uses. For the temporary relief of. : 1 Cough with Sputum and Sinus congestion.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-125-12</NDCCode>
    <PackageDescription>120 mL in 1 BOTTLE (82797-125-12) </PackageDescription>
    <NDC11Code>82797-0125-12</NDC11Code>
    <ProductNDC>82797-125</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>K Flush</ProprietaryName>
    <NonProprietaryName>Belladonna, Berberls Vulgarls, Cantharis, , Hydrangea, Parelra Brava, Rubla Tinct, Solidago, Sarsaparilla, Urtica Urens</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240404</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>BELLADONNA LEAF; BERBERIS VULGARIS FRUIT; HYDRANGEA ARBORESCENS BARK; LYTTA VESICATORIA; RUBIA CORDIFOLIA ROOT; SARSAPARILLA; SOLIDAGO CANADENSIS FLOWERING TOP; URTICA URENS FLOWER</SubstanceName>
    <StrengthNumber>.12; 1.7; .492; .492; .24; .24; .24; .24</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240404</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>It is indicated for removal of kidney, ureter and bladder stones as well as related infection, inflammation and burning sensation during urination.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-127-12</NDCCode>
    <PackageDescription>120 mL in 1 BOTTLE (82797-127-12) </PackageDescription>
    <NDC11Code>82797-0127-12</NDC11Code>
    <ProductNDC>82797-127</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Alfalfa Tonic</ProprietaryName>
    <NonProprietaryName>Alfalfa, China Off, Avena Sativa, Hydrastis Can, Calc Phos, Kali Phos, Nat Phos, Mag Phos, Ferr Phos, Ferric Citrate, Acidum Phos</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240516</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>ALFALFA; AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; CINCHONA BARK; DIBASIC POTASSIUM PHOSPHATE; FERRIC CITRATE ANHYDROUS; FERROUS PHOSPHATE; HYDRASTIS CANADENSIS WHOLE; MAGNESIUM PHOSPHATE, DIBASIC; PHOSPHORIC ACID; SODIUM PHOSPHATE</SubstanceName>
    <StrengthNumber>4.2; 2.4; .48; 3; .48; 3; .48; 1.44; .48; .36; .48</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Pharm_Classes>Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Osmotic Activity [MoA], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240516</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Indications and Usage. Convalescence, General weakness, Nervous debility, loss of appetite, anemia, and chlorosis.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-129-12</NDCCode>
    <PackageDescription>120 mL in 1 BOTTLE, PLASTIC (82797-129-12) </PackageDescription>
    <NDC11Code>82797-0129-12</NDC11Code>
    <ProductNDC>82797-129</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Alfalfa Plus Ginseng Syrup</ProprietaryName>
    <NonProprietaryName>Alfalfa, China Off, Avena Sativa, Hydrastis Can, Ginseng, Ferric Citrate, Nat Phos, Mag Phos, Calc Phos, Kali Phos, Ferr Phos,</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240704</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>ALFALFA; AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; CINCHONA OFFICINALIS WHOLE; DIBASIC POTASSIUM PHOSPHATE; FERRIC CITRATE ANHYDROUS; FERROUS SULFATE; HYDRASTIS CANADENSIS WHOLE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PANAX GINSENG WHOLE; SODIUM PHOSPHATE</SubstanceName>
    <StrengthNumber>4.32; 2.4; .48; 3.84; .48; 3; .48; 1.44; .48; 2.16; .48</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Pharm_Classes>Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240704</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Convalescence, General weakness, Nervous debility, loss of appetite, boost immunity, anemia and chlorosis. Improves appetite and helps in digestion resulting in improved mental and physical health and weight gain.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-130-12</NDCCode>
    <PackageDescription>120 mL in 1 BOTTLE, PLASTIC (82797-130-12) </PackageDescription>
    <NDC11Code>82797-0130-12</NDC11Code>
    <ProductNDC>82797-130</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Androtone Syrup</ProprietaryName>
    <NonProprietaryName>Tribulus Terr, Avena Sativa,sterculia Acum, Nuphar Lut, Sabal Serr, Agnus Cast, Lycopodium Clav, Gentiana Lut, Yohimbinum, Lecithin, Natrum Phos, Kali Phos, Calcarea Phos, Natrum Mur, Strychninum Sulph, Acidum Phos, Choloformum</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240708</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>AVENA SATIVA WHOLE; CALCIUM PHOSPHATE; COLA ACUMINATA WHOLE; GENTIANA LUTEA WHOLE; LECITHIN, SOYBEAN; LYCOPODIUM CLAVATUM WHOLE; MONOBASIC POTASSIUM PHOSPHATE; NUPHAR LUTEA WHOLE; PHOSPHORIC ACID; SABAL PALMETTO WHOLE; SODIUM CHLORIDE; SODIUM PHOSPHATE; STRYCHNINE; TRIBULUS TERRESTRIS WHOLE; VITEX AGNUS-CASTUS WHOLE; YOHIMBINE</SubstanceName>
    <StrengthNumber>.08; .005; .03; .01; .0625; .01; .005; .03; .01; .03; .005; .005; .015; .08; .02; .01</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Pharm_Classes>Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240708</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Indicated in loss of sex drive and erectile dysfunction. Helpful for those who want to build their muscles. Also increases testosterone levels in the bloodstream.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-131-01</NDCCode>
    <PackageDescription>1 BOTTLE in 1 BOX (82797-131-01)  / 120 mL in 1 BOTTLE (82797-131-12) </PackageDescription>
    <NDC11Code>82797-0131-01</NDC11Code>
    <ProductNDC>82797-131</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Nefritol Syrup</ProprietaryName>
    <NonProprietaryName>Berberis Vulgaris 8x, Epigea Repens, Apis Mellifica 6, Hydrangea Arborescens , Cantharis 30 , Pareira Brava 3, Lycopodium Clav , Solidago Virgaurea</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20250422</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>CHONDRODENDRON TOMENTOSUM ROOT; HYDRANGEA ARBORESCENS WHOLE; EPIGAEA REPENS; APIS MELLIFERA; BERBERIS VULGARIS WHOLE; LYTTA VESICATORIA; SOLIDAGO VIRGAUREA WHOLE; LYCOPODIUM CLAVATUM WHOLE</SubstanceName>
    <StrengthNumber>.0027; .0075; .0027; .0075; .0075; .005; .0027; .0025</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</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>Deprecated</Status>
    <LastUpdate>2026-08-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250422</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>it is indicated for the supportive treatment of conditions related to urinary tract including its infections, pain and inflammation.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-132-01</NDCCode>
    <PackageDescription>1 BOTTLE in 1 BOX (82797-132-01)  / 120 mL in 1 BOTTLE (82797-132-12) </PackageDescription>
    <NDC11Code>82797-0132-01</NDC11Code>
    <ProductNDC>82797-132</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Vitmin C</ProprietaryName>
    <NonProprietaryName>Acid Phos D3, Cocculus D5, Helonias Dioca D5, Zincum Met D6, Citrus Limonum , Rosa Canina , Ascorbic Acid, Citric Acid</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20250424</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>ROSA CANINA WHOLE; ZINC; ASCORBIC ACID; STRYCHNOS IGNATII WHOLE; CITRUS LIMON WHOLE; CHAMAELIRIUM LUTEUM WHOLE; ANAMIRTA COCCULUS WHOLE; PHOSPHORIC ACID</SubstanceName>
    <StrengthNumber>.01; 7.5; .01; .003; .01; .01; .01; .01</StrengthNumber>
    <StrengthUnit>mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL; mg/120mL</StrengthUnit>
    <Pharm_Classes>Ascorbic Acid [CS], Vitamin C [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-08-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250424</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Conditions of Nervous Exhaustion. General Neurasthenia. Insomnia. Fatigue. Lack of Energy. Inability to concentrate.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-333-12</NDCCode>
    <PackageDescription>30 g in 1 BOTTLE, GLASS (82797-333-12) </PackageDescription>
    <NDC11Code>82797-0333-12</NDC11Code>
    <ProductNDC>82797-333</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Masood Abrotanum</ProprietaryName>
    <NonProprietaryName>Abrotanum</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20230201</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>ARTEMISIA ABROTANUM FLOWERING TOP</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/30g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2025-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>To be used for acute, self-limiting conditions according to standard homeopathic indications.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>33342-128-12</NDCCode>
    <PackageDescription>10 BLISTER PACK in 1 CARTON (33342-128-12)  &gt; 10 TABLET in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>33342-0128-12</NDC11Code>
    <ProductNDC>33342-128</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Telmisartan And Hydrochlorothiazide</ProprietaryName>
    <NonProprietaryName>Telmisartan And Hydrochlorothiazide</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151102</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA204169</ApplicationNumber>
    <LabelerName>Macleods Pharmaceuticals Limited</LabelerName>
    <SubstanceName>TELMISARTAN; HYDROCHLOROTHIAZIDE</SubstanceName>
    <StrengthNumber>40; 12.5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2020-09-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20151102</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>42939-128-12</NDCCode>
    <PackageDescription>3785 mL in 1 BOTTLE, PLASTIC (42939-128-12) </PackageDescription>
    <NDC11Code>42939-0128-12</NDC11Code>
    <ProductNDC>42939-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Scrub, Scrub-stat, Foam Safe, Micro-guard</ProprietaryName>
    <NonProprietaryName>Chlorhexidine Gluconate</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>19860722</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA019258</ApplicationNumber>
    <LabelerName>AVA, Inc.</LabelerName>
    <SubstanceName>CHLORHEXIDINE GLUCONATE</SubstanceName>
    <StrengthNumber>40</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Decreased Cell Wall Integrity [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-05-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>19860722</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care . healthcare personnel handwash: handwash to help reduce bacteria that potentially can cause disease . skin wound and general cleanser: helps reduce bacteria on the skin .</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>46063-552-12</NDCCode>
    <PackageDescription>128 g in 1 CAN (46063-552-12) </PackageDescription>
    <NDC11Code>46063-0552-12</NDC11Code>
    <ProductNDC>46063-552</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Relispray Antifungal Powder</ProprietaryName>
    <NonProprietaryName>Miconazole Nitrate</NonProprietaryName>
    <DosageFormName>AEROSOL, SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20220301</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M005</ApplicationNumber>
    <LabelerName>Midas-Care Pharmaceuticals Pvt. Ltd.</LabelerName>
    <SubstanceName>MICONAZOLE NITRATE</SubstanceName>
    <StrengthNumber>.02</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <Pharm_Classes>Azole Antifungal [EPC], Azoles [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220301</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>effectively treats most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). relieves itching, scaling, burning and discomfort which may accompany these conditions.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>46063-810-12</NDCCode>
    <PackageDescription>128 g in 1 CAN (46063-810-12) </PackageDescription>
    <NDC11Code>46063-0810-12</NDC11Code>
    <ProductNDC>46063-810</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Relispray Antifungal Liquid</ProprietaryName>
    <NonProprietaryName>Tolnaftate</NonProprietaryName>
    <DosageFormName>AEROSOL, SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20220301</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M005</ApplicationNumber>
    <LabelerName>Midas-Care Pharmaceuticals Pvt. Ltd.</LabelerName>
    <SubstanceName>TOLNAFTATE</SubstanceName>
    <StrengthNumber>.01</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220301</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>effectively treats most athlete's foot (tinea pedis), jock itch (tinea cruris), and ringworm (tinea corporis). relieves itching, scaling, burning and discomfort which may accompany these conditions.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>49348-128-12</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (49348-128-12)  &gt; 60 TABLET, FILM COATED in 1 BOTTLE</PackageDescription>
    <NDC11Code>49348-0128-12</NDC11Code>
    <ProductNDC>49348-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunmark Acid Reducer</ProprietaryName>
    <NonProprietaryName>Famotidine</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20090910</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA075400</ApplicationNumber>
    <LabelerName>Strategic Sourcing Services LLC</LabelerName>
    <SubstanceName>FAMOTIDINE</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20090910</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>relieves heartburn associated with acid indigestion and sour stomach. prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>50804-128-02</NDCCode>
    <PackageDescription>2 BLISTER PACK in 1 CARTON (50804-128-02)  / 12 TABLET, COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>50804-0128-02</NDC11Code>
    <ProductNDC>50804-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Allergy Multi Symptom</ProprietaryName>
    <NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20200801</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M012</ApplicationNumber>
    <LabelerName>GOODSENSE</LabelerName>
    <SubstanceName>ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 2; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-10-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20200801</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily relieves these symptoms of hay fever or other upper respiratory allergies: headachenasal congestionsinus congestion and pressureminor aches and painsrunny nose and sneezing. helps clear nasal passages. helps decongest sinus openings and passages. temporarily relieves these additional symptoms of hay fever:  itching of the nose or throatitchy, watery eyes.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>57344-128-02</NDCCode>
    <PackageDescription>2 BLISTER PACK in 1 CARTON (57344-128-02)  &gt; 12 TABLET, COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>57344-0128-02</NDC11Code>
    <ProductNDC>57344-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride</ProprietaryName>
    <NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20120802</StartMarketingDate>
    <EndMarketingDate>20220630</EndMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part341</ApplicationNumber>
    <LabelerName>AAA Pharmaceutical, Inc.</LabelerName>
    <SubstanceName>ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 2; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2022-07-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20120802</StartMarketingDatePackage>
    <EndMarketingDatePackage>20220630</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>57344-128-06</NDCCode>
    <PackageDescription>4 BLISTER PACK in 1 CARTON (57344-128-06)  &gt; 12 TABLET, COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>57344-0128-06</NDC11Code>
    <ProductNDC>57344-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride</ProprietaryName>
    <NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20121228</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part341</ApplicationNumber>
    <LabelerName>AAA Pharmaceutical, Inc.</LabelerName>
    <SubstanceName>ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 2; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-10-17</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20121228</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>58159-128-12</NDCCode>
    <PackageDescription>.001 kg in 1 DRUM (58159-128-12) </PackageDescription>
    <NDC11Code>58159-0128-12</NDC11Code>
    <ProductNDC>58159-128</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Eltrombopag Choline</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20250724</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>NURAY CHEMICALS PRIVATE LIMITED</LabelerName>
    <SubstanceName>ELTROMBOPAG CHOLINE</SubstanceName>
    <StrengthNumber>35</StrengthNumber>
    <StrengthUnit>kg/35kg</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2025-08-05</LastUpdate>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>24-JUL-25</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>58411-128-30</NDCCode>
    <PackageDescription>1 TRAY in 1 CARTON (58411-128-30)  &gt; 12 g in 1 TRAY</PackageDescription>
    <NDC11Code>58411-0128-30</NDC11Code>
    <ProductNDC>58411-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Shiseido Uv Protective Compact (refill)</ProprietaryName>
    <ProprietaryNameSuffix>Dark Beige</ProprietaryNameSuffix>
    <NonProprietaryName>Octinoxate, Octocrylene, And Titanium Dioxide</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20140201</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>SHISEIDO AMERICAS CORPORATION</LabelerName>
    <SubstanceName>OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE</SubstanceName>
    <StrengthNumber>888; 600; 1416</StrengthNumber>
    <StrengthUnit>mg/12g; mg/12g; mg/12g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20140201</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>63187-128-12</NDCCode>
    <PackageDescription>12 TABLET, FILM COATED in 1 BOTTLE (63187-128-12) </PackageDescription>
    <NDC11Code>63187-0128-12</NDC11Code>
    <ProductNDC>63187-128</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Ketorolac Tromethamine</ProprietaryName>
    <NonProprietaryName>Ketorolac Tromethamine</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19980617</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA074754</ApplicationNumber>
    <LabelerName>Proficient Rx LP</LabelerName>
    <SubstanceName>KETOROLAC TROMETHAMINE</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitor [EPC], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2022-04-12</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220208</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Carefully consider the potential benefits and risks of Ketorolac Tromethamine Tablets USP and other treatment options before deciding to use Ketorolac Tromethamine Tablets USP. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals.</IndicationAndUsage>
    <Description>Ketorolac Tromethamine Tablets USP are a member of the pyrrolo-pyrrole group of non-steroidal anti-inflammatory drugs (NSAIDs). The chemical name for ketorolac tromethamine, USP is (±)-5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid, compound with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1). The structural formula is. C15H13NO3 .C4H11NO3 M.W. 376.40. Ketorolac tromethamine, USP is a racemic mixture of [-]S and [+]R ketorolac tromethamine, USP. Ketorolac tromethamine, USP may exist in three crystal forms. All forms are equally soluble in water. Ketorolac tromethamine, USP has a pKa of 3.5 and an n-octanol/water partition coefficient of 0.26. Ketorolac Tromethamine Tablets USP are white, round, convex, unscored, film coated tablets. Each tablet, for oral administration, contains 10 mg ketorolac tromethamine, USP, the active ingredient. In addition, each tablet contains the following inactive ingredients: hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, and titanium dioxide.</Description>
  </NDC>
  <NDC>
    <NDCCode>68998-128-02</NDCCode>
    <PackageDescription>2 BLISTER PACK in 1 CARTON (68998-128-02)  &gt; 12 TABLET, COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>68998-0128-02</NDC11Code>
    <ProductNDC>68998-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Allergy Multi-symptom</ProprietaryName>
    <NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20100601</StartMarketingDate>
    <EndMarketingDate>20211231</EndMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part341</ApplicationNumber>
    <LabelerName>Marc Glassman, Inc.</LabelerName>
    <SubstanceName>ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 2; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2022-01-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20100601</StartMarketingDatePackage>
    <EndMarketingDatePackage>20211231</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>71406-128-12</NDCCode>
    <PackageDescription>120 TABLET, DELAYED RELEASE in 1 BOTTLE (71406-128-12) </PackageDescription>
    <NDC11Code>71406-0128-12</NDC11Code>
    <ProductNDC>71406-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Aspirin 81 Mg</ProprietaryName>
    <NonProprietaryName>Aspirin Enteric Coated Tablets 81 Mg</NonProprietaryName>
    <DosageFormName>TABLET, DELAYED RELEASE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20210503</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M013</ApplicationNumber>
    <LabelerName>AACE Pharmaceuticals, Inc.</LabelerName>
    <SubstanceName>ASPIRIN</SubstanceName>
    <StrengthNumber>81</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2025-05-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20210514</StartMarketingDatePackage>
    <SamplePackage>Y</SamplePackage>
    <IndicationAndUsage>Pin Reliever.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>72476-128-02</NDCCode>
    <PackageDescription>2 BLISTER PACK in 1 CARTON (72476-128-02)  / 12 TABLET, COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>72476-0128-02</NDC11Code>
    <ProductNDC>72476-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Allergy Multisymptom</ProprietaryName>
    <NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20201021</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M012</ApplicationNumber>
    <LabelerName>RETAIL BUSINESS SERVICES , LLC.</LabelerName>
    <SubstanceName>ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 2; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-10-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20201021</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily relieves these symptoms of hay fever or other upper respiratory allergies: headachesinus congestion and pressurenasal congestionrunny nose and sneezingminor aches and pains. temporarily relieves these additional symptoms of hay fever: itching of the nose or throatitchy, watery eyes. helps clear nasal passages. helps decongest sinus openings and passages.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>72520-121-12</NDCCode>
    <PackageDescription>128 g in 1 TUBE (72520-121-12) </PackageDescription>
    <NDC11Code>72520-0121-12</NDC11Code>
    <ProductNDC>72520-121</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Nuvalu Creamy Petroleum</ProprietaryName>
    <NonProprietaryName>Petrolatum</NonProprietaryName>
    <DosageFormName>JELLY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20231101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M016</ApplicationNumber>
    <LabelerName>JC SALES</LabelerName>
    <SubstanceName>PETROLATUM</SubstanceName>
    <StrengthNumber>30</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20231101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>75603-128-12</NDCCode>
    <PackageDescription>3785 mL in 1 JUG (75603-128-12) </PackageDescription>
    <NDC11Code>75603-0128-12</NDC11Code>
    <ProductNDC>75603-128</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Hand Sanitizer</ProprietaryName>
    <NonProprietaryName>Alcohol</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20200330</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part333A</ApplicationNumber>
    <LabelerName>BLACK BAND, LLC.</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>80</StrengthNumber>
    <StrengthUnit>mL/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2022-01-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20200330</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>76176-230-12</NDCCode>
    <PackageDescription>128 g in 1 TUBE (76176-230-12) </PackageDescription>
    <NDC11Code>76176-0230-12</NDC11Code>
    <ProductNDC>76176-230</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Nuvalu Creamy Petroleum</ProprietaryName>
    <NonProprietaryName>Petrolatum</NonProprietaryName>
    <DosageFormName>JELLY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20231101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M016</ApplicationNumber>
    <LabelerName>Ningbo Liyuan Daily Chemical Products Co.,Ltd.</LabelerName>
    <SubstanceName>PETROLATUM</SubstanceName>
    <StrengthNumber>30</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-12-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20231101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily protects minor: cuts, scrapes, burns. temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>82797-423-30</NDCCode>
    <PackageDescription>30 mg in 1 BLISTER PACK (82797-423-30) </PackageDescription>
    <NDC11Code>82797-0423-30</NDC11Code>
    <ProductNDC>82797-423</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Enerjizer</ProprietaryName>
    <NonProprietaryName>Avena Sativa, Alfalfa, Echinacea, Ginkgo Biloba, Ginseng Panax, Caffeinum, Gentiana Lut, Sterculia Acum, Calcium Phosphate, Chromium Oxide, Cobaltum Met, Cuprum Sulphuricum, Iodium, Lecithinum, Manganese Sulphate, Magnesium Oxide, Kali Muriaticum, Selenium, Zinc Sulphate</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240715</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Dr. Masood Homeopathic Pharmaceuticals Private Limited</LabelerName>
    <SubstanceName>ALFALFA; AVENA SATIVA WHOLE; BASIC COPPER SULFATE; CAFFEINE; CALCIUM PHOSPHATE; CHROMIC OXIDE; COBALT; COLA ACUMINATA WHOLE; ECHINACEA, UNSPECIFIED; GENTIANA LUTEA WHOLE; GINKGO BILOBA WHOLE; IODINE; LECITHIN, SOYBEAN; MAGNESIUM OXIDE; MANGANESE SULFATE; PANAX GINSENG WHOLE; POTASSIUM CHLORIDE; SELENIUM; ZINC SULFATE</SubstanceName>
    <StrengthNumber>.11392; .11392; .00128; .192; .128; .00128; .00128; .0576; .0576; .0576; .0128; .0128; .064; .0128; .0128; .0128; .0128; .0032; .0192</StrengthNumber>
    <StrengthUnit>mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg; mg/660mg</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cell-mediated Immunity [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Methylxanthine [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Xanthines [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2026-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240715</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Restores the lost vigour and vitality. Bad effects of prolonged illness. Mental fatigue or exhaustion. Acts as prophylactic against viral diseases. Lowers cholesterol and control glucose level in body. Reduce inflammation in body. Helpful in regulation of blood pressure and reduce fatigue. Keeps you energetic during exercise. Makes muscles stronger. Fulfill iodine deficiency and helpful in thyroid gland functioning. Prevents from cerebral thrombosis and stroke.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>0096-0741-04</NDCCode>
    <PackageDescription>128 g in 1 BOTTLE (0096-0741-04) </PackageDescription>
    <NDC11Code>00096-0741-04</NDC11Code>
    <ProductNDC>0096-0741</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Solbar Fifty Spf50</ProprietaryName>
    <NonProprietaryName>Solbar Fifty Spf50</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>19960601</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M020</ApplicationNumber>
    <LabelerName>Person and Covey</LabelerName>
    <SubstanceName>OCTOCRYLENE; OCTINOXATE; OXYBENZONE; AVOBENZONE</SubstanceName>
    <StrengthNumber>.1; .08; .06; .011</StrengthNumber>
    <StrengthUnit>g/g; g/g; g/g; g/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-12-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>19960601</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early skin aging caused by the sun.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>0338-0147-03</NDCCode>
    <PackageDescription>24 BAG in 1 CARTON (0338-0147-03)  &gt; 500 mL in 1 BAG</PackageDescription>
    <NDC11Code>00338-0147-03</NDC11Code>
    <ProductNDC>0338-0147</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Plasma-lyte 56 And Dextrose</ProprietaryName>
    <NonProprietaryName>Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>19790201</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA017385</ApplicationNumber>
    <LabelerName>Baxter Healthcare Corporation</LabelerName>
    <SubstanceName>DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM ACETATE; MAGNESIUM ACETATE TETRAHYDRATE</SubstanceName>
    <StrengthNumber>5; 234; 128; 32</StrengthNumber>
    <StrengthUnit>g/100mL; mg/100mL; mg/100mL; mg/100mL</StrengthUnit>
    <Pharm_Classes>Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2015-12-18</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0338-0147-04</NDCCode>
    <PackageDescription>14 BAG in 1 CARTON (0338-0147-04)  &gt; 1000 mL in 1 BAG</PackageDescription>
    <NDC11Code>00338-0147-04</NDC11Code>
    <ProductNDC>0338-0147</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Plasma-lyte 56 And Dextrose</ProprietaryName>
    <NonProprietaryName>Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>19790201</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA017385</ApplicationNumber>
    <LabelerName>Baxter Healthcare Corporation</LabelerName>
    <SubstanceName>DEXTROSE MONOHYDRATE; SODIUM CHLORIDE; POTASSIUM ACETATE; MAGNESIUM ACETATE TETRAHYDRATE</SubstanceName>
    <StrengthNumber>5; 234; 128; 32</StrengthNumber>
    <StrengthUnit>g/100mL; mg/100mL; mg/100mL; mg/100mL</StrengthUnit>
    <Pharm_Classes>Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2016-12-27</LastUpdate>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>82797-128-12</NDCCode><ProprietaryName>Menola Tonic</ProprietaryName><NonProprietaryName>Moringa Olifera, Avena Sativa, Ginseng, Acidum Lacticum, Nicotinamide, Thiamine Hydrochloride, Riboflavin</NonProprietaryName></NDC><NDC><NDCCode>82797-123-12</NDCCode><ProprietaryName>Masood Ivypan Cough Syrup</ProprietaryName><NonProprietaryName>Hedera Helix</NonProprietaryName></NDC><NDC><NDCCode>82797-125-12</NDCCode><ProprietaryName>K Flush</ProprietaryName><NonProprietaryName>Belladonna, Berberls Vulgarls, Cantharis, , Hydrangea, Parelra Brava, Rubla Tinct, Solidago, Sarsaparilla, Urtica Urens</NonProprietaryName></NDC><NDC><NDCCode>82797-127-12</NDCCode><ProprietaryName>Alfalfa Tonic</ProprietaryName><NonProprietaryName>Alfalfa, China Off, Avena Sativa, Hydrastis Can, Calc Phos, Kali Phos, Nat Phos, Mag Phos, Ferr Phos, Ferric Citrate, Acidum Phos</NonProprietaryName></NDC><NDC><NDCCode>82797-129-12</NDCCode><ProprietaryName>Alfalfa Plus Ginseng Syrup</ProprietaryName><NonProprietaryName>Alfalfa, China Off, Avena Sativa, Hydrastis Can, Ginseng, Ferric Citrate, Nat Phos, Mag Phos, Calc Phos, Kali Phos, Ferr Phos,</NonProprietaryName></NDC><NDC><NDCCode>82797-130-12</NDCCode><ProprietaryName>Androtone Syrup</ProprietaryName><NonProprietaryName>Tribulus Terr, Avena Sativa,sterculia Acum, Nuphar Lut, Sabal Serr, Agnus Cast, Lycopodium Clav, Gentiana Lut, Yohimbinum, Lecithin, Natrum Phos, Kali Phos, Calcarea Phos, Natrum Mur, Strychninum Sulph, Acidum Phos, Choloformum</NonProprietaryName></NDC><NDC><NDCCode>82797-131-01</NDCCode><ProprietaryName>Nefritol Syrup</ProprietaryName><NonProprietaryName>Berberis Vulgaris 8x, Epigea Repens, Apis Mellifica 6, Hydrangea Arborescens , Cantharis 30 , Pareira Brava 3, Lycopodium Clav , Solidago Virgaurea</NonProprietaryName></NDC><NDC><NDCCode>82797-132-01</NDCCode><ProprietaryName>Vitmin C</ProprietaryName><NonProprietaryName>Acid Phos D3, Cocculus D5, Helonias Dioca D5, Zincum Met D6, Citrus Limonum , Rosa Canina , Ascorbic Acid, Citric Acid</NonProprietaryName></NDC><NDC><NDCCode>82797-333-12</NDCCode><ProprietaryName>Masood Abrotanum</ProprietaryName><NonProprietaryName>Abrotanum</NonProprietaryName></NDC><NDC><NDCCode>33342-128-12</NDCCode><ProprietaryName>Telmisartan And Hydrochlorothiazide</ProprietaryName><NonProprietaryName>Telmisartan And Hydrochlorothiazide</NonProprietaryName></NDC><NDC><NDCCode>42939-128-12</NDCCode><ProprietaryName>Scrub, Scrub-stat, Foam Safe, Micro-guard</ProprietaryName><NonProprietaryName>Chlorhexidine Gluconate</NonProprietaryName></NDC><NDC><NDCCode>46063-552-12</NDCCode><ProprietaryName>Relispray Antifungal Powder</ProprietaryName><NonProprietaryName>Miconazole Nitrate</NonProprietaryName></NDC><NDC><NDCCode>46063-810-12</NDCCode><ProprietaryName>Relispray Antifungal Liquid</ProprietaryName><NonProprietaryName>Tolnaftate</NonProprietaryName></NDC><NDC><NDCCode>49348-128-12</NDCCode><ProprietaryName>Sunmark Acid Reducer</ProprietaryName><NonProprietaryName>Famotidine</NonProprietaryName></NDC><NDC><NDCCode>50804-128-02</NDCCode><ProprietaryName>Allergy Multi Symptom</ProprietaryName><NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>57344-128-02</NDCCode><ProprietaryName>Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride</ProprietaryName><NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>57344-128-06</NDCCode><ProprietaryName>Acetaminophen, Chlorpheniramine Maleate, Phenylephrine Hydrochloride</ProprietaryName><NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>58159-128-12</NDCCode><NonProprietaryName>Eltrombopag Choline</NonProprietaryName></NDC><NDC><NDCCode>58411-128-30</NDCCode><ProprietaryName>Shiseido Uv Protective Compact (refill)</ProprietaryName><NonProprietaryName>Octinoxate, Octocrylene, And Titanium Dioxide</NonProprietaryName></NDC><NDC><NDCCode>63187-128-12</NDCCode><ProprietaryName>Ketorolac Tromethamine</ProprietaryName><NonProprietaryName>Ketorolac Tromethamine</NonProprietaryName></NDC><NDC><NDCCode>68998-128-02</NDCCode><ProprietaryName>Allergy Multi-symptom</ProprietaryName><NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>71406-128-12</NDCCode><ProprietaryName>Aspirin 81 Mg</ProprietaryName><NonProprietaryName>Aspirin Enteric Coated Tablets 81 Mg</NonProprietaryName></NDC><NDC><NDCCode>72476-128-02</NDCCode><ProprietaryName>Allergy Multisymptom</ProprietaryName><NonProprietaryName>Acetaminophen, Chlorpheniramine Maleate, And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>72520-121-12</NDCCode><ProprietaryName>Nuvalu Creamy Petroleum</ProprietaryName><NonProprietaryName>Petrolatum</NonProprietaryName></NDC><NDC><NDCCode>75603-128-12</NDCCode><ProprietaryName>Hand Sanitizer</ProprietaryName><NonProprietaryName>Alcohol</NonProprietaryName></NDC><NDC><NDCCode>76176-230-12</NDCCode><ProprietaryName>Nuvalu Creamy Petroleum</ProprietaryName><NonProprietaryName>Petrolatum</NonProprietaryName></NDC><NDC><NDCCode>82797-423-30</NDCCode><ProprietaryName>Enerjizer</ProprietaryName><NonProprietaryName>Avena Sativa, Alfalfa, Echinacea, Ginkgo Biloba, Ginseng Panax, Caffeinum, Gentiana Lut, Sterculia Acum, Calcium Phosphate, Chromium Oxide, Cobaltum Met, Cuprum Sulphuricum, Iodium, Lecithinum, Manganese Sulphate, Magnesium Oxide, Kali Muriaticum, Selenium, Zinc Sulphate</NonProprietaryName></NDC><NDC><NDCCode>0096-0741-04</NDCCode><ProprietaryName>Solbar Fifty Spf50</ProprietaryName><NonProprietaryName>Solbar Fifty Spf50</NonProprietaryName></NDC><NDC><NDCCode>0338-0147-03</NDCCode><ProprietaryName>Plasma-lyte 56 And Dextrose</ProprietaryName><NonProprietaryName>Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate</NonProprietaryName></NDC><NDC><NDCCode>0338-0147-04</NDCCode><ProprietaryName>Plasma-lyte 56 And Dextrose</ProprietaryName><NonProprietaryName>Dextrose Monohydrate, Sodium Chloride, Potassium Acetate, Magnesium Acetate Tetrahydrate</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",
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      "LicenseNumber2": "25MA07672000",
      "LicenseNumberStateCode2": "NJ",
      "PrimaryTaxonomySwitch2": "Y"
    },
    {
      "NPI": "1184645301",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "BAIK",
      "FirstName": "RANIA",
      "Credential": "D.O.",
      "FirstLineMailingAddress": "602 ROUTE 169",
      "SecondLineMailingAddress": "PO BOX 865",
      "MailingAddressCityName": "WOODSTOCK",
      "MailingAddressStateName": "CT",
      "MailingAddressPostalCode": "06281-2225",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "860-821-3406",
      "MailingAddressFaxNumber": "860-821-3407",
      "FirstLinePracticeLocationAddress": "602 ROUTE 169",
      "PracticeLocationAddressCityName": "WOODSTOCK",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06281-2225",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "860-821-3406",
      "PracticeLocationAddressFaxNumber": "860-821-3407",
      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

                
{
  "NPI": [
    {
      "NPI": "1083349906",
      "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",
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}
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