RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (23 ms elapsed)

{
  "NDC": [
    {
      "NDCCode": "62864-909-16",
      "PackageDescription": "500 mL in 1 BOTTLE (62864-909-16)",
      "NDC11Code": "62864-0909-16",
      "ProductNDC": "62864-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Anticavity Fluoride Rinse",
      "ProprietaryNameSuffix": "Alcohol And Sugar Free",
      "NonProprietaryName": "Sodium Fluoride",
      "DosageFormName": "LIQUID",
      "RouteName": "DENTAL",
      "StartMarketingDate": "20151005",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "62864-662-16",
      "PackageDescription": "473 mL in 1 BOTTLE (62864-662-16)",
      "NDC11Code": "62864-0662-16",
      "ProductNDC": "62864-662",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141023",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-10-11",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "62864-665-16",
      "PackageDescription": "473 mL in 1 BOTTLE (62864-665-16)",
      "NDC11Code": "62864-0665-16",
      "ProductNDC": "62864-665",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse Clean And Fresh",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151002",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "Uses. Aids in the prevention of dental cavities."
    },
    {
      "NDCCode": "62864-759-16",
      "PackageDescription": "473.2 mL in 1 BOTTLE (62864-759-16)",
      "NDC11Code": "62864-0759-16",
      "ProductNDC": "62864-759",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Alcohol Free Antiseptic Rinse",
      "ProprietaryNameSuffix": "For All Mouth Sores",
      "NonProprietaryName": "Hydrogen Peroxide 1.5%, Menthol 0.1%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141101",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part356",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "HYDROGEN PEROXIDE; MENTHOL",
      "StrengthNumber": "1.5; 1",
      "StrengthUnit": "mL/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231",
      "IndicationAndUsage": "Uses: 1 first aid to help reduce bacteria in minor oral wounds, 2 for temporary pain relief and, 3 use in cleansing minor wounds or minor gum inflammation resulting from:, 4 minor dental procedures, 5 accidental injury, 6 orthodontic appliances, 7 canker sores, 8 dentures, 9 other irritations of the mouth and gums."
    },
    {
      "NDCCode": "62864-760-16",
      "PackageDescription": "473.2 mL in 1 BOTTLE (62864-760-16)",
      "NDC11Code": "62864-0760-16",
      "ProductNDC": "62864-760",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Antiseptic Rinse",
      "ProprietaryNameSuffix": "For All Mouth Sores",
      "NonProprietaryName": "Hydrogen Peroxide 1.5%, Menthol 0.1%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141101",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part356",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "HYDROGEN PEROXIDE; MENTHOL",
      "StrengthNumber": "1.5; 1",
      "StrengthUnit": "mL/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "Uses: 1 first aid to help reduce bacteria in minor oral wounds, 2 for temporary pain relief and, 3 use in cleansing minor wounds or minor gum inflammation resulting from:, 4 minor dental procedures, 5 accidental injury, 6 orthodontic appliances, 7 canker sores, 8 dentures, 9 other irritations of the mouth and gums."
    },
    {
      "NDCCode": "62864-764-16",
      "PackageDescription": "473.2 mL in 1 BOTTLE (62864-764-16) ",
      "NDC11Code": "62864-0764-16",
      "ProductNDC": "62864-764",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Toothache Rinse",
      "NonProprietaryName": "Benzyl Alcohol, Zinc Chloride",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20161201",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part356",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "BENZYL ALCOHOL; ZINC CHLORIDE",
      "StrengthNumber": "2.7; 1.5",
      "StrengthUnit": "mg/mL; mg/mL",
      "Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Pediculicide [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2023-01-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20221231",
      "StartMarketingDatePackage": "20161201",
      "SamplePackage": "N",
      "IndicationAndUsage": "Use for temporary relief of pain due to toothaches, minor irritation of the mouth and gums, occasional minor irritation, pain, sore mouth and sore throat."
    },
    {
      "NDCCode": "62864-910-16",
      "PackageDescription": "500 mL in 1 BOTTLE (62864-910-16)",
      "NDC11Code": "62864-0910-16",
      "ProductNDC": "62864-910",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Anticavity Fluoride Rinse",
      "ProprietaryNameSuffix": "Alcohol And Sugar Free",
      "NonProprietaryName": "Sodium Fluoride",
      "DosageFormName": "LIQUID",
      "RouteName": "DENTAL",
      "StartMarketingDate": "20151005",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "10237-909-16",
      "PackageDescription": "500 mL in 1 BOTTLE (10237-909-16)",
      "NDC11Code": "10237-0909-16",
      "ProductNDC": "10237-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Anticavity Fluoride Rinse",
      "ProprietaryNameSuffix": "Alcohol And Sugar Free",
      "NonProprietaryName": "Sodium Fluoride",
      "DosageFormName": "LIQUID",
      "RouteName": "DENTAL",
      "StartMarketingDate": "20151005",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Co., Inc.",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "11084-909-16",
      "PackageDescription": "454 g in 1 CAN (11084-909-16) ",
      "NDC11Code": "11084-0909-16",
      "ProductNDC": "11084-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Alcare Plus Foaming Antiseptic Handrub",
      "NonProprietaryName": "Alcohol",
      "DosageFormName": "AEROSOL, FOAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20250801",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "505G(a)(3)",
      "LabelerName": "SC Johnson Professional USA Inc",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "59.7",
      "StrengthUnit": "g/100g",
      "Status": "Active",
      "LastUpdate": "2025-10-08",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20250801",
      "SamplePackage": "N",
      "IndicationAndUsage": "Surgical Scrub significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care. Healthcare Personnel Handwash to decrease transient bacteria on the skin before contact with patients under medical care or treatment."
    },
    {
      "NDCCode": "12634-909-16",
      "PackageDescription": "473 mL in 1 BOTTLE (12634-909-16)",
      "NDC11Code": "12634-0909-16",
      "ProductNDC": "12634-909",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Promethazine Hydrochloride And Codeine Phosphate",
      "NonProprietaryName": "Promethazine Hydrochloride And Codeine Phosphate",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "19970826",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA040151",
      "LabelerName": "Apotheca Inc",
      "SubstanceName": "CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE",
      "StrengthNumber": "10; 6.25",
      "StrengthUnit": "mg/5mL; mg/5mL",
      "Pharm_Classes": "Full Opioid Agonists [MoA],Opioid Agonist [EPC],Phenothiazine [EPC],Phenothiazines [CS]",
      "DEASchedule": "CV",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "Promethazine hydrochloride and codeine phosphate syrup is indicated for the temporary relief of coughs and upper respiratory symptoms associated with allergy or the common cold.",
      "Description": "Each 5 mL (one teaspoonful), for oral administration contains: Promethazine hydrochloride 6.25 mg; codeine phosphate 10 mg. Alcohol 7%. Inactive Ingredients: Artificial boysenberry flavor, ascorbic acid, citric acid, D&C Red No. 33, FD&C Blue No. 1, FD&C Yellow No. 6, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, sodium benzoate, sodium citrate, and sucrose syrup. Codeine is one of the naturally occurring phenanthrene alkaloids of opium derived from the nopium poppy; it is classified pharmacologically as a narcotic analgesic. Codeine phosphate may be chemically designated as 7,8-Didehydro-4, 5α-epoxy- 3-methoxy-17-methylmorphinan-6α-ol phosphate (1:1)(salt) hemihydrate. The phosphate salt of codeine occurs as white, needle-shaped crystals or white crystalline powder. Codeine phosphate is freely soluble in water and slightly soluble in alcohol. It has a molecular weight of 406.37, a molecular formula of C 18H 21NO 3 H 3PO 4  ½ H 20, and the following structural formula:. Promethazine hydrochloride, a phenothiazine derivative, is chemically designated as (±)-10-[2-(Dimethylamino)propyl] phenothiazine monohydrochloride. Promethazine hydrochloride occurs as a white to faint yellow, practically odorless, crystalline powder which slowly oxidizes and turns blue on prolonged exposure to air. It is soluble in water and freely soluble in alcohol. It has a molecular weight of 320.88, a molecular formula of C 17H 20N 2SHCl, and the following structural formula:."
    },
    {
      "NDCCode": "50474-909-16",
      "PackageDescription": "473 mL in 1 BOTTLE (50474-909-16)",
      "NDC11Code": "50474-0909-16",
      "ProductNDC": "50474-909",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Lortab",
      "NonProprietaryName": "Hydrocodone Bitartrate And Acetaminophen",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930308",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA081051",
      "LabelerName": "UCB, Inc.",
      "SubstanceName": "ACETAMINOPHEN; HYDROCODONE BITARTRATE",
      "StrengthNumber": "500; 7.5",
      "StrengthUnit": "mg/15mL; mg/15mL",
      "Pharm_Classes": "Opioid Agonist [EPC],Opioid Agonists [MoA]",
      "DEASchedule": "CIII",
      "Status": "Deprecated",
      "LastUpdate": "2014-04-22"
    },
    {
      "NDCCode": "51414-909-16",
      "PackageDescription": "20 g in 1 BOTTLE (51414-909-16) ",
      "NDC11Code": "51414-0909-16",
      "ProductNDC": "51414-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Pain Relieving Burn Gel",
      "NonProprietaryName": "Burn Gel",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20190101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part346",
      "LabelerName": "Yuyao Jessie Commodity Co.,Ltd.",
      "SubstanceName": "LIDOCAINE",
      "StrengthNumber": "2",
      "StrengthUnit": "g/100g",
      "Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2024-02-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20190104",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporary relief from minor aches and pains of sore muscles &joints associated with arthritis ,backache,strains,sprains."
    },
    {
      "NDCCode": "66651-909-16",
      "PackageDescription": "30 kg in 1 DRUM (66651-909-16) ",
      "NDC11Code": "66651-0909-16",
      "ProductNDC": "66651-909",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Memantine Hydrochloride",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20150123",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "HIKAL LIMITED",
      "SubstanceName": "MEMANTINE HYDROCHLORIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "kg/kg",
      "Status": "Unfinished",
      "LastUpdate": "2024-02-23",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "23-JAN-15"
    },
    {
      "NDCCode": "62864-901-25",
      "PackageDescription": "74 mL in 1 BOTTLE, WITH APPLICATOR (62864-901-25)",
      "NDC11Code": "62864-0901-25",
      "ProductNDC": "62864-901",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Arrid Xx Roll On",
      "ProprietaryNameSuffix": "Antiperspirant Deodorant Regular",
      "NonProprietaryName": "Aluminum Chlorohydrate",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "19960716",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part350",
      "LabelerName": ".Church & Dwight Canada Corp",
      "SubstanceName": "ALUMINUM CHLOROHYDRATE",
      "StrengthNumber": "16",
      "StrengthUnit": "1/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "reduces underarm perspiration."
    },
    {
      "NDCCode": "14803-909-00",
      "PackageDescription": "14400 CAPSULE, LIQUID FILLED in 1 BOX (14803-909-00) ",
      "NDC11Code": "14803-0909-00",
      "ProductNDC": "14803-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "NonProprietaryName": "Acetaminophen, Dextromethorphan Hydrobromide And Phenylephrine Hydrochloride",
      "DosageFormName": "CAPSULE, LIQUID FILLED",
      "StartMarketingDate": "20240301",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Elysium Pharmaceuticals Ltd",
      "SubstanceName": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE",
      "StrengthNumber": "325; 10; 5",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Status": "Unfinished",
      "LastUpdate": "2026-02-16",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "01-MAR-24"
    },
    {
      "NDCCode": "19515-909-52",
      "PackageDescription": "10 SYRINGE in 1 CARTON (19515-909-52)  > .5 mL in 1 SYRINGE (19515-909-41) ",
      "NDC11Code": "19515-0909-52",
      "ProductNDC": "19515-909",
      "ProductTypeName": "VACCINE",
      "ProprietaryName": "Flulaval Quadrivalent",
      "ProprietaryNameSuffix": "2018/2019",
      "NonProprietaryName": "Influenza Virus Vaccine",
      "DosageFormName": "SUSPENSION",
      "RouteName": "INTRAMUSCULAR",
      "StartMarketingDate": "20180629",
      "EndMarketingDate": "20190630",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125163",
      "LabelerName": "ID Biomedical Corporation of Quebec",
      "SubstanceName": "INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 IVR-186 (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MARYLAND/15/2016 BX-69A ANTIGEN (UV, FORMALDEHYDE INACTIVATED)",
      "StrengthNumber": "15; 15; 15; 15",
      "StrengthUnit": "ug/.5mL; ug/.5mL; ug/.5mL; ug/.5mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-07-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20180629",
      "EndMarketingDatePackage": "20190630",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "49035-909-30",
      "PackageDescription": "1 BOTTLE, PLASTIC in 1 CARTON (49035-909-30)  > 177 mL in 1 BOTTLE, PLASTIC",
      "NDC11Code": "49035-0909-30",
      "ProductNDC": "49035-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "All Day Moisture",
      "NonProprietaryName": "Octinoxate, Zinc Oxide",
      "DosageFormName": "LOTION",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20090512",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Wal-Mart",
      "SubstanceName": "OCTINOXATE; ZINC OXIDE",
      "StrengthNumber": "61.2; 30.6",
      "StrengthUnit": "mg/mL; mg/mL",
      "Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2024-10-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20090512",
      "SamplePackage": "N",
      "IndicationAndUsage": "helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the rise of skin cancer and early skin aging caused by the sun."
    },
    {
      "NDCCode": "59735-909-02",
      "PackageDescription": "1 TUBE in 1 BOX (59735-909-02)  / 35 mL in 1 TUBE (59735-909-01) ",
      "NDC11Code": "59735-0909-02",
      "ProductNDC": "59735-909",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Protectint 34c",
      "NonProprietaryName": "Homosalate, Octisalate, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20231122",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M020",
      "LabelerName": "PML NYC, LLC",
      "SubstanceName": "HOMOSALATE; ZINC OXIDE; OCTISALATE",
      "StrengthNumber": "7; 13.58; 5",
      "StrengthUnit": "g/100mL; g/100mL; g/100mL",
      "Status": "Active",
      "LastUpdate": "2026-04-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20231122",
      "SamplePackage": "N",
      "IndicationAndUsage": "Stop use and ask a doctorif rash occurs."
    },
    {
      "NDCCode": "67254-909-01",
      "PackageDescription": "60 kg in 1 DRUM (67254-909-01) ",
      "NDC11Code": "67254-0909-01",
      "ProductNDC": "67254-909",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Lumefantrine",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20130116",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "Zhejiang Medicine Co., Ltd. Xinchang Pharmaceutical Factory",
      "SubstanceName": "LUMEFANTRINE",
      "StrengthNumber": "1",
      "StrengthUnit": "kg/kg",
      "Status": "Unfinished",
      "LastUpdate": "2024-01-08",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "16-JAN-13"
    },
    {
      "NDCCode": "69097-909-50",
      "PackageDescription": "1 KIT in 1 CARTON (69097-909-50)  *  2 mL in 1 VIAL, SINGLE-DOSE (69097-950-32)  *  2 mL in 1 SYRINGE (69097-960-31) ",
      "NDC11Code": "69097-0909-50",
      "ProductNDC": "69097-909",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Leuprolide Acetate Depot",
      "NonProprietaryName": "Leuprolide Acetate",
      "DosageFormName": "KIT",
      "StartMarketingDate": "20220715",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA205054",
      "LabelerName": "CIPLA USA INC.",
      "Status": "Active",
      "LastUpdate": "2024-09-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220715",
      "SamplePackage": "N",
      "IndicationAndUsage": "LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration (leuprolide acetate) is indicated for treatment of advanced prostate cancer.",
      "Description": "Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-releasing hormone (GnRH). The analog possesses greater potency than the natural hormone. The chemical name is 5-oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-D-leucyl-L-leucyl-L-arginyl-N-ethyl-L-prolinamide acetate (salt) with the following structural formula. Where: n=1 or 2. Leuprolide acetate has a molecular weight of 1209.41 as free base”. Leuprolide is freely soluble in water. LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration is available in a vial containing white to off white sterile lyophilized microspheres together with the corresponding sterile reconstitution diluent in a pre-filled syringe. When LEUPROLIDE ACETATE FOR DEPOT SUSPENSION and the diluent are mixed together they become a suspension intended as an intramuscular injection to be given ONCE EVERY 12 WEEKS as a single dose. Each vial of LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration delivers leuprolide acetate (22.5 mg), polylactic acid (188.4 mg), triethylcitrate (10.4 mg), polysorbate 80 (3.8 mg), mannitol (88.4 mg) and carmellose sodium (25 mg). The prefilled syringe containing the clear reconstitution diluent (2 mL) contains mannitol (16 mg), water for injections, and sodium hydroxide and hydrochloric acid to control pH. Leuprolide acetate for depot suspension is an extended release sterile, single dose injection in suspension form for intramuscular administration."
    },
    {
      "NDCCode": "71288-909-10",
      "PackageDescription": "1 VIAL, GLASS in 1 CARTON (71288-909-10)  / 10 mL in 1 VIAL, GLASS",
      "NDC11Code": "71288-0909-10",
      "ProductNDC": "71288-909",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Insulin Diluting Medium For Garzulys",
      "NonProprietaryName": "Water Injection",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAVENOUS; SUBCUTANEOUS",
      "StartMarketingDate": "20260724",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA761497",
      "LabelerName": "Meitheal Pharmaceuticals Inc.",
      "SubstanceName": "WATER",
      "StrengthNumber": "1",
      "StrengthUnit": "mL/mL",
      "Status": "Active",
      "LastUpdate": "2026-08-05",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260724",
      "SamplePackage": "N",
      "IndicationAndUsage": "Garzulys is indicated to improve glycemic control in adults and pediatric patients with diabetes mellitus.",
      "Description": "Insulin aspart-fsan is a rapid-acting human insulin analog homologous with regular human insulin with the exception of a single substitution of the amino acid proline by aspartic acid in position B28, and is produced by recombinant DNA technology utilizing Escherichia coli. Insulin aspart-fsan has the empirical formula C256H381N65079S6 and a molecular weight of 5825.8 Da. Figure 1. Structural formula of insulin aspart-fsan. Garzulys (insulin aspart-fsan) injection is a sterile, clear, and colorless solution for subcutaneous or intravenous use. Each mL contains 100 units of insulin aspart-fsan and the inactive ingredients: dibasic sodium phosphate (0.997 mg), glycerin (16 mg), metacresol (1.72 mg), phenol (1.5 mg), sodium chloride (0.58 mg), zinc (19.6 mcg), and Water for Injection, USP. Garzulys has a pH of 7.2-7.6. Hydrochloric acid and/or sodium hydroxide may be added to adjust pH."
    },
    {
      "NDCCode": "62864-662-01",
      "PackageDescription": "47.31 mL in 1 BOTTLE (62864-662-01)",
      "NDC11Code": "62864-0662-01",
      "ProductNDC": "62864-662",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141023",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2015-12-18"
    },
    {
      "NDCCode": "62864-662-08",
      "PackageDescription": "237 mL in 1 BOTTLE (62864-662-08)",
      "NDC11Code": "62864-0662-08",
      "ProductNDC": "62864-662",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141023",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-10-11",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "62864-662-32",
      "PackageDescription": "946 mL in 1 BOTTLE (62864-662-32)",
      "NDC11Code": "62864-0662-32",
      "ProductNDC": "62864-662",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20141023",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-10-11",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "62864-665-08",
      "PackageDescription": "237 mL in 1 BOTTLE (62864-665-08)",
      "NDC11Code": "62864-0665-08",
      "ProductNDC": "62864-665",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Truly Radiant",
      "ProprietaryNameSuffix": "Whitening And Strengthening Rinse Clean And Fresh",
      "NonProprietaryName": "Sodium Fluoride 0.02%",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151002",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part355",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "SODIUM FLUORIDE",
      "StrengthNumber": ".2",
      "StrengthUnit": "mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "Uses. Aids in the prevention of dental cavities."
    },
    {
      "NDCCode": "62864-764-08",
      "PackageDescription": "237 mL in 1 BOTTLE (62864-764-08) ",
      "NDC11Code": "62864-0764-08",
      "ProductNDC": "62864-764",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Orajel Toothache Rinse",
      "NonProprietaryName": "Benzyl Alcohol, Zinc Chloride",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20161201",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part356",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "BENZYL ALCOHOL; ZINC CHLORIDE",
      "StrengthNumber": "2.7; 1.5",
      "StrengthUnit": "mg/mL; mg/mL",
      "Pharm_Classes": "Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Pediculicide [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2023-01-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20221231",
      "StartMarketingDatePackage": "20181224",
      "SamplePackage": "N",
      "IndicationAndUsage": "Use for temporary relief of pain due to toothaches, minor irritation of the mouth and gums, occasional minor irritation, pain, sore mouth and sore throat."
    },
    {
      "NDCCode": "62864-900-19",
      "PackageDescription": "56 mL in 1 BOTTLE, WITH APPLICATOR (62864-900-19)",
      "NDC11Code": "62864-0900-19",
      "ProductNDC": "62864-900",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Ultramax Roll On",
      "ProprietaryNameSuffix": "Antiperspirant Deodorant Powder Fresh",
      "NonProprietaryName": "Aluminum Zirconium Tetrachlorohydrex Gly",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20000728",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part350",
      "LabelerName": "Church & Dwight Canada Corp",
      "SubstanceName": "ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY",
      "StrengthNumber": "21",
      "StrengthUnit": "g/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2015-12-25"
    },
    {
      "NDCCode": "62864-902-10",
      "PackageDescription": "1 JAR in 1 CARTON (62864-902-10)  > 28 g in 1 JAR",
      "NDC11Code": "62864-0902-10",
      "ProductNDC": "62864-902",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Arrid Extra Dry",
      "ProprietaryNameSuffix": "Antiperspirant Deodorant",
      "NonProprietaryName": "Aluminum Sesquichlorohydrate 17%",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "19951108",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part350",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "ALUMINUM SESQUICHLOROHYDRATE",
      "StrengthNumber": "170",
      "StrengthUnit": "mg/g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231",
      "IndicationAndUsage": "reduces underarm perspiration."
    },
    {
      "NDCCode": "62864-903-00",
      "PackageDescription": "1 BOTTLE, PLASTIC in 1 CARTON (62864-903-00)  > 125 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC",
      "NDC11Code": "62864-0903-00",
      "ProductNDC": "62864-903",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Baby Orajel Naturals",
      "ProprietaryNameSuffix": "For Teething Pain Relief",
      "NonProprietaryName": "Calcarea Phosphorica, Coffea Cruda, Chamomilla",
      "DosageFormName": "TABLET, ORALLY DISINTEGRATING",
      "RouteName": "SUBLINGUAL",
      "StartMarketingDate": "20110615",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "TRIBASIC CALCIUM PHOSPHATE; ARABICA COFFEE BEAN; MATRICARIA RECUTITA",
      "StrengthNumber": "3; 3; 3",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "62864-903-12",
      "PackageDescription": "1 BOTTLE, PLASTIC in 1 CARTON (62864-903-12)  > 125 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC",
      "NDC11Code": "62864-0903-12",
      "ProductNDC": "62864-903",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Baby Orajel Naturals",
      "ProprietaryNameSuffix": "For Teething Pain Relief",
      "NonProprietaryName": "Calcarea Phosphorica, Coffea Cruda, Chamomilla",
      "DosageFormName": "TABLET, ORALLY DISINTEGRATING",
      "RouteName": "SUBLINGUAL",
      "StartMarketingDate": "20110615",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Church & Dwight Canada Corp.",
      "SubstanceName": "TRIBASIC CALCIUM PHOSPHATE; ARABICA COFFEE BEAN; MATRICARIA RECUTITA",
      "StrengthNumber": "3; 3; 3",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    }
  ]
}
                    

{"NDC":[{"NDCCode":"62864-909-16","ProprietaryName":"Orajel Anticavity Fluoride Rinse","NonProprietaryName":"Sodium Fluoride"},{"NDCCode":"62864-662-16","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-665-16","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-759-16","ProprietaryName":"Orajel Alcohol Free Antiseptic Rinse","NonProprietaryName":"Hydrogen Peroxide 1.5%, Menthol 0.1%"},{"NDCCode":"62864-760-16","ProprietaryName":"Orajel Antiseptic Rinse","NonProprietaryName":"Hydrogen Peroxide 1.5%, Menthol 0.1%"},{"NDCCode":"62864-764-16","ProprietaryName":"Orajel Toothache Rinse","NonProprietaryName":"Benzyl Alcohol, Zinc Chloride"},{"NDCCode":"62864-910-16","ProprietaryName":"Orajel Anticavity Fluoride Rinse","NonProprietaryName":"Sodium Fluoride"},{"NDCCode":"10237-909-16","ProprietaryName":"Orajel Anticavity Fluoride Rinse","NonProprietaryName":"Sodium Fluoride"},{"NDCCode":"11084-909-16","ProprietaryName":"Alcare Plus Foaming Antiseptic Handrub","NonProprietaryName":"Alcohol"},{"NDCCode":"12634-909-16","ProprietaryName":"Promethazine Hydrochloride And Codeine Phosphate","NonProprietaryName":"Promethazine Hydrochloride And Codeine Phosphate"},{"NDCCode":"50474-909-16","ProprietaryName":"Lortab","NonProprietaryName":"Hydrocodone Bitartrate And Acetaminophen"},{"NDCCode":"51414-909-16","ProprietaryName":"Pain Relieving Burn Gel","NonProprietaryName":"Burn Gel"},{"NDCCode":"66651-909-16","NonProprietaryName":"Memantine Hydrochloride"},{"NDCCode":"62864-901-25","ProprietaryName":"Arrid Xx Roll On","NonProprietaryName":"Aluminum Chlorohydrate"},{"NDCCode":"14803-909-00","NonProprietaryName":"Acetaminophen, Dextromethorphan Hydrobromide And Phenylephrine Hydrochloride"},{"NDCCode":"19515-909-52","ProprietaryName":"Flulaval Quadrivalent","NonProprietaryName":"Influenza Virus Vaccine"},{"NDCCode":"49035-909-30","ProprietaryName":"All Day Moisture","NonProprietaryName":"Octinoxate, Zinc Oxide"},{"NDCCode":"59735-909-02","ProprietaryName":"Protectint 34c","NonProprietaryName":"Homosalate, Octisalate, Zinc Oxide"},{"NDCCode":"67254-909-01","NonProprietaryName":"Lumefantrine"},{"NDCCode":"69097-909-50","ProprietaryName":"Leuprolide Acetate Depot","NonProprietaryName":"Leuprolide Acetate"},{"NDCCode":"71288-909-10","ProprietaryName":"Insulin Diluting Medium For Garzulys","NonProprietaryName":"Water Injection"},{"NDCCode":"62864-662-01","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-662-08","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-662-32","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-665-08","ProprietaryName":"Truly Radiant","NonProprietaryName":"Sodium Fluoride 0.02%"},{"NDCCode":"62864-764-08","ProprietaryName":"Orajel Toothache Rinse","NonProprietaryName":"Benzyl Alcohol, Zinc Chloride"},{"NDCCode":"62864-900-19","ProprietaryName":"Ultramax Roll On","NonProprietaryName":"Aluminum Zirconium Tetrachlorohydrex Gly"},{"NDCCode":"62864-902-10","ProprietaryName":"Arrid Extra Dry","NonProprietaryName":"Aluminum Sesquichlorohydrate 17%"},{"NDCCode":"62864-903-00","ProprietaryName":"Baby Orajel Naturals","NonProprietaryName":"Calcarea Phosphorica, Coffea Cruda, Chamomilla"},{"NDCCode":"62864-903-12","ProprietaryName":"Baby Orajel Naturals","NonProprietaryName":"Calcarea Phosphorica, Coffea Cruda, Chamomilla"}]}
                    

<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <NDC>
    <NDCCode>62864-909-16</NDCCode>
    <PackageDescription>500 mL in 1 BOTTLE (62864-909-16)</PackageDescription>
    <NDC11Code>62864-0909-16</NDC11Code>
    <ProductNDC>62864-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName>
    <ProprietaryNameSuffix>Alcohol And Sugar Free</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>DENTAL</RouteName>
    <StartMarketingDate>20151005</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62864-662-16</NDCCode>
    <PackageDescription>473 mL in 1 BOTTLE (62864-662-16)</PackageDescription>
    <NDC11Code>62864-0662-16</NDC11Code>
    <ProductNDC>62864-662</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141023</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-10-11</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62864-665-16</NDCCode>
    <PackageDescription>473 mL in 1 BOTTLE (62864-665-16)</PackageDescription>
    <NDC11Code>62864-0665-16</NDC11Code>
    <ProductNDC>62864-665</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse Clean And Fresh</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151002</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Uses. Aids in the prevention of dental cavities.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-759-16</NDCCode>
    <PackageDescription>473.2 mL in 1 BOTTLE (62864-759-16)</PackageDescription>
    <NDC11Code>62864-0759-16</NDC11Code>
    <ProductNDC>62864-759</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Alcohol Free Antiseptic Rinse</ProprietaryName>
    <ProprietaryNameSuffix>For All Mouth Sores</ProprietaryNameSuffix>
    <NonProprietaryName>Hydrogen Peroxide 1.5%, Menthol 0.1%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part356</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>HYDROGEN PEROXIDE; MENTHOL</SubstanceName>
    <StrengthNumber>1.5; 1</StrengthNumber>
    <StrengthUnit>mL/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Uses: 1 first aid to help reduce bacteria in minor oral wounds, 2 for temporary pain relief and, 3 use in cleansing minor wounds or minor gum inflammation resulting from:, 4 minor dental procedures, 5 accidental injury, 6 orthodontic appliances, 7 canker sores, 8 dentures, 9 other irritations of the mouth and gums.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-760-16</NDCCode>
    <PackageDescription>473.2 mL in 1 BOTTLE (62864-760-16)</PackageDescription>
    <NDC11Code>62864-0760-16</NDC11Code>
    <ProductNDC>62864-760</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Antiseptic Rinse</ProprietaryName>
    <ProprietaryNameSuffix>For All Mouth Sores</ProprietaryNameSuffix>
    <NonProprietaryName>Hydrogen Peroxide 1.5%, Menthol 0.1%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part356</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>HYDROGEN PEROXIDE; MENTHOL</SubstanceName>
    <StrengthNumber>1.5; 1</StrengthNumber>
    <StrengthUnit>mL/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Uses: 1 first aid to help reduce bacteria in minor oral wounds, 2 for temporary pain relief and, 3 use in cleansing minor wounds or minor gum inflammation resulting from:, 4 minor dental procedures, 5 accidental injury, 6 orthodontic appliances, 7 canker sores, 8 dentures, 9 other irritations of the mouth and gums.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-764-16</NDCCode>
    <PackageDescription>473.2 mL in 1 BOTTLE (62864-764-16) </PackageDescription>
    <NDC11Code>62864-0764-16</NDC11Code>
    <ProductNDC>62864-764</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Toothache Rinse</ProprietaryName>
    <NonProprietaryName>Benzyl Alcohol, Zinc Chloride</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20161201</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part356</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>BENZYL ALCOHOL; ZINC CHLORIDE</SubstanceName>
    <StrengthNumber>2.7; 1.5</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL</StrengthUnit>
    <Pharm_Classes>Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Pediculicide [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2023-01-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20221231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20161201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Use for temporary relief of pain due to toothaches, minor irritation of the mouth and gums, occasional minor irritation, pain, sore mouth and sore throat.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-910-16</NDCCode>
    <PackageDescription>500 mL in 1 BOTTLE (62864-910-16)</PackageDescription>
    <NDC11Code>62864-0910-16</NDC11Code>
    <ProductNDC>62864-910</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName>
    <ProprietaryNameSuffix>Alcohol And Sugar Free</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>DENTAL</RouteName>
    <StartMarketingDate>20151005</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>10237-909-16</NDCCode>
    <PackageDescription>500 mL in 1 BOTTLE (10237-909-16)</PackageDescription>
    <NDC11Code>10237-0909-16</NDC11Code>
    <ProductNDC>10237-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName>
    <ProprietaryNameSuffix>Alcohol And Sugar Free</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>DENTAL</RouteName>
    <StartMarketingDate>20151005</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Co., Inc.</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>11084-909-16</NDCCode>
    <PackageDescription>454 g in 1 CAN (11084-909-16) </PackageDescription>
    <NDC11Code>11084-0909-16</NDC11Code>
    <ProductNDC>11084-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Alcare Plus Foaming Antiseptic Handrub</ProprietaryName>
    <NonProprietaryName>Alcohol</NonProprietaryName>
    <DosageFormName>AEROSOL, FOAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20250801</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>505G(a)(3)</ApplicationNumber>
    <LabelerName>SC Johnson Professional USA Inc</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>59.7</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-10-08</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250801</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Surgical Scrub significantly reduces the number of micro-organisms on the hands and forearms prior to surgery or patient care. Healthcare Personnel Handwash to decrease transient bacteria on the skin before contact with patients under medical care or treatment.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>12634-909-16</NDCCode>
    <PackageDescription>473 mL in 1 BOTTLE (12634-909-16)</PackageDescription>
    <NDC11Code>12634-0909-16</NDC11Code>
    <ProductNDC>12634-909</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Promethazine Hydrochloride And Codeine Phosphate</ProprietaryName>
    <NonProprietaryName>Promethazine Hydrochloride And Codeine Phosphate</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19970826</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA040151</ApplicationNumber>
    <LabelerName>Apotheca Inc</LabelerName>
    <SubstanceName>CODEINE PHOSPHATE; PROMETHAZINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>10; 6.25</StrengthNumber>
    <StrengthUnit>mg/5mL; mg/5mL</StrengthUnit>
    <Pharm_Classes>Full Opioid Agonists [MoA],Opioid Agonist [EPC],Phenothiazine [EPC],Phenothiazines [CS]</Pharm_Classes>
    <DEASchedule>CV</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Promethazine hydrochloride and codeine phosphate syrup is indicated for the temporary relief of coughs and upper respiratory symptoms associated with allergy or the common cold.</IndicationAndUsage>
    <Description>Each 5 mL (one teaspoonful), for oral administration contains: Promethazine hydrochloride 6.25 mg; codeine phosphate 10 mg. Alcohol 7%. Inactive Ingredients: Artificial boysenberry flavor, ascorbic acid, citric acid, D&amp;C Red No. 33, FD&amp;C Blue No. 1, FD&amp;C Yellow No. 6, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, sodium benzoate, sodium citrate, and sucrose syrup. Codeine is one of the naturally occurring phenanthrene alkaloids of opium derived from the nopium poppy; it is classified pharmacologically as a narcotic analgesic. Codeine phosphate may be chemically designated as 7,8-Didehydro-4, 5α-epoxy- 3-methoxy-17-methylmorphinan-6α-ol phosphate (1:1)(salt) hemihydrate. The phosphate salt of codeine occurs as white, needle-shaped crystals or white crystalline powder. Codeine phosphate is freely soluble in water and slightly soluble in alcohol. It has a molecular weight of 406.37, a molecular formula of C 18H 21NO 3 H 3PO 4  ½ H 20, and the following structural formula:. Promethazine hydrochloride, a phenothiazine derivative, is chemically designated as (±)-10-[2-(Dimethylamino)propyl] phenothiazine monohydrochloride. Promethazine hydrochloride occurs as a white to faint yellow, practically odorless, crystalline powder which slowly oxidizes and turns blue on prolonged exposure to air. It is soluble in water and freely soluble in alcohol. It has a molecular weight of 320.88, a molecular formula of C 17H 20N 2SHCl, and the following structural formula:.</Description>
  </NDC>
  <NDC>
    <NDCCode>50474-909-16</NDCCode>
    <PackageDescription>473 mL in 1 BOTTLE (50474-909-16)</PackageDescription>
    <NDC11Code>50474-0909-16</NDC11Code>
    <ProductNDC>50474-909</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Lortab</ProprietaryName>
    <NonProprietaryName>Hydrocodone Bitartrate And Acetaminophen</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930308</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA081051</ApplicationNumber>
    <LabelerName>UCB, Inc.</LabelerName>
    <SubstanceName>ACETAMINOPHEN; HYDROCODONE BITARTRATE</SubstanceName>
    <StrengthNumber>500; 7.5</StrengthNumber>
    <StrengthUnit>mg/15mL; mg/15mL</StrengthUnit>
    <Pharm_Classes>Opioid Agonist [EPC],Opioid Agonists [MoA]</Pharm_Classes>
    <DEASchedule>CIII</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2014-04-22</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>51414-909-16</NDCCode>
    <PackageDescription>20 g in 1 BOTTLE (51414-909-16) </PackageDescription>
    <NDC11Code>51414-0909-16</NDC11Code>
    <ProductNDC>51414-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Pain Relieving Burn Gel</ProprietaryName>
    <NonProprietaryName>Burn Gel</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20190101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part346</ApplicationNumber>
    <LabelerName>Yuyao Jessie Commodity Co.,Ltd.</LabelerName>
    <SubstanceName>LIDOCAINE</SubstanceName>
    <StrengthNumber>2</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Pharm_Classes>Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2024-02-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190104</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporary relief from minor aches and pains of sore muscles &amp;joints associated with arthritis ,backache,strains,sprains.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>66651-909-16</NDCCode>
    <PackageDescription>30 kg in 1 DRUM (66651-909-16) </PackageDescription>
    <NDC11Code>66651-0909-16</NDC11Code>
    <ProductNDC>66651-909</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Memantine Hydrochloride</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20150123</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>HIKAL LIMITED</LabelerName>
    <SubstanceName>MEMANTINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>kg/kg</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2024-02-23</LastUpdate>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>23-JAN-15</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>62864-901-25</NDCCode>
    <PackageDescription>74 mL in 1 BOTTLE, WITH APPLICATOR (62864-901-25)</PackageDescription>
    <NDC11Code>62864-0901-25</NDC11Code>
    <ProductNDC>62864-901</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Arrid Xx Roll On</ProprietaryName>
    <ProprietaryNameSuffix>Antiperspirant Deodorant Regular</ProprietaryNameSuffix>
    <NonProprietaryName>Aluminum Chlorohydrate</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>19960716</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part350</ApplicationNumber>
    <LabelerName>.Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>ALUMINUM CHLOROHYDRATE</SubstanceName>
    <StrengthNumber>16</StrengthNumber>
    <StrengthUnit>1/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>reduces underarm perspiration.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>14803-909-00</NDCCode>
    <PackageDescription>14400 CAPSULE, LIQUID FILLED in 1 BOX (14803-909-00) </PackageDescription>
    <NDC11Code>14803-0909-00</NDC11Code>
    <ProductNDC>14803-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <NonProprietaryName>Acetaminophen, Dextromethorphan Hydrobromide And Phenylephrine Hydrochloride</NonProprietaryName>
    <DosageFormName>CAPSULE, LIQUID FILLED</DosageFormName>
    <StartMarketingDate>20240301</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Elysium Pharmaceuticals Ltd</LabelerName>
    <SubstanceName>ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>325; 10; 5</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2026-02-16</LastUpdate>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>01-MAR-24</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>19515-909-52</NDCCode>
    <PackageDescription>10 SYRINGE in 1 CARTON (19515-909-52)  &gt; .5 mL in 1 SYRINGE (19515-909-41) </PackageDescription>
    <NDC11Code>19515-0909-52</NDC11Code>
    <ProductNDC>19515-909</ProductNDC>
    <ProductTypeName>VACCINE</ProductTypeName>
    <ProprietaryName>Flulaval Quadrivalent</ProprietaryName>
    <ProprietaryNameSuffix>2018/2019</ProprietaryNameSuffix>
    <NonProprietaryName>Influenza Virus Vaccine</NonProprietaryName>
    <DosageFormName>SUSPENSION</DosageFormName>
    <RouteName>INTRAMUSCULAR</RouteName>
    <StartMarketingDate>20180629</StartMarketingDate>
    <EndMarketingDate>20190630</EndMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125163</ApplicationNumber>
    <LabelerName>ID Biomedical Corporation of Quebec</LabelerName>
    <SubstanceName>INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 IVR-186 (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (UV, FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MARYLAND/15/2016 BX-69A ANTIGEN (UV, FORMALDEHYDE INACTIVATED)</SubstanceName>
    <StrengthNumber>15; 15; 15; 15</StrengthNumber>
    <StrengthUnit>ug/.5mL; ug/.5mL; ug/.5mL; ug/.5mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-07-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20180629</StartMarketingDatePackage>
    <EndMarketingDatePackage>20190630</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>49035-909-30</NDCCode>
    <PackageDescription>1 BOTTLE, PLASTIC in 1 CARTON (49035-909-30)  &gt; 177 mL in 1 BOTTLE, PLASTIC</PackageDescription>
    <NDC11Code>49035-0909-30</NDC11Code>
    <ProductNDC>49035-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>All Day Moisture</ProprietaryName>
    <NonProprietaryName>Octinoxate, Zinc Oxide</NonProprietaryName>
    <DosageFormName>LOTION</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20090512</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Wal-Mart</LabelerName>
    <SubstanceName>OCTINOXATE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>61.2; 30.6</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL</StrengthUnit>
    <Pharm_Classes>Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2024-10-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20090512</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases the rise of skin cancer and early skin aging caused by the sun.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>59735-909-02</NDCCode>
    <PackageDescription>1 TUBE in 1 BOX (59735-909-02)  / 35 mL in 1 TUBE (59735-909-01) </PackageDescription>
    <NDC11Code>59735-0909-02</NDC11Code>
    <ProductNDC>59735-909</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Protectint 34c</ProprietaryName>
    <NonProprietaryName>Homosalate, Octisalate, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20231122</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M020</ApplicationNumber>
    <LabelerName>PML NYC, LLC</LabelerName>
    <SubstanceName>HOMOSALATE; ZINC OXIDE; OCTISALATE</SubstanceName>
    <StrengthNumber>7; 13.58; 5</StrengthNumber>
    <StrengthUnit>g/100mL; g/100mL; g/100mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-04-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20231122</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Stop use and ask a doctorif rash occurs.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>67254-909-01</NDCCode>
    <PackageDescription>60 kg in 1 DRUM (67254-909-01) </PackageDescription>
    <NDC11Code>67254-0909-01</NDC11Code>
    <ProductNDC>67254-909</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Lumefantrine</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20130116</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>Zhejiang Medicine Co., Ltd. Xinchang Pharmaceutical Factory</LabelerName>
    <SubstanceName>LUMEFANTRINE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>kg/kg</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2024-01-08</LastUpdate>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>16-JAN-13</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>69097-909-50</NDCCode>
    <PackageDescription>1 KIT in 1 CARTON (69097-909-50)  *  2 mL in 1 VIAL, SINGLE-DOSE (69097-950-32)  *  2 mL in 1 SYRINGE (69097-960-31) </PackageDescription>
    <NDC11Code>69097-0909-50</NDC11Code>
    <ProductNDC>69097-909</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Leuprolide Acetate Depot</ProprietaryName>
    <NonProprietaryName>Leuprolide Acetate</NonProprietaryName>
    <DosageFormName>KIT</DosageFormName>
    <StartMarketingDate>20220715</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA205054</ApplicationNumber>
    <LabelerName>CIPLA USA INC.</LabelerName>
    <Status>Active</Status>
    <LastUpdate>2024-09-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220715</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration (leuprolide acetate) is indicated for treatment of advanced prostate cancer.</IndicationAndUsage>
    <Description>Leuprolide acetate is a synthetic nonapeptide analog of naturally occurring gonadotropin-releasing hormone (GnRH). The analog possesses greater potency than the natural hormone. The chemical name is 5-oxo-L-prolyl-L-histidyl-L-tryptophyl-L-seryl-L-tyrosyl-D-leucyl-L-leucyl-L-arginyl-N-ethyl-L-prolinamide acetate (salt) with the following structural formula. Where: n=1 or 2. Leuprolide acetate has a molecular weight of 1209.41 as free base”. Leuprolide is freely soluble in water. LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration is available in a vial containing white to off white sterile lyophilized microspheres together with the corresponding sterile reconstitution diluent in a pre-filled syringe. When LEUPROLIDE ACETATE FOR DEPOT SUSPENSION and the diluent are mixed together they become a suspension intended as an intramuscular injection to be given ONCE EVERY 12 WEEKS as a single dose. Each vial of LEUPROLIDE ACETATE FOR DEPOT SUSPENSION 22.5 mg for 3-month administration delivers leuprolide acetate (22.5 mg), polylactic acid (188.4 mg), triethylcitrate (10.4 mg), polysorbate 80 (3.8 mg), mannitol (88.4 mg) and carmellose sodium (25 mg). The prefilled syringe containing the clear reconstitution diluent (2 mL) contains mannitol (16 mg), water for injections, and sodium hydroxide and hydrochloric acid to control pH. Leuprolide acetate for depot suspension is an extended release sterile, single dose injection in suspension form for intramuscular administration.</Description>
  </NDC>
  <NDC>
    <NDCCode>71288-909-10</NDCCode>
    <PackageDescription>1 VIAL, GLASS in 1 CARTON (71288-909-10)  / 10 mL in 1 VIAL, GLASS</PackageDescription>
    <NDC11Code>71288-0909-10</NDC11Code>
    <ProductNDC>71288-909</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Insulin Diluting Medium For Garzulys</ProprietaryName>
    <NonProprietaryName>Water Injection</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAVENOUS; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20260724</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA761497</ApplicationNumber>
    <LabelerName>Meitheal Pharmaceuticals Inc.</LabelerName>
    <SubstanceName>WATER</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mL/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-08-05</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260724</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Garzulys is indicated to improve glycemic control in adults and pediatric patients with diabetes mellitus.</IndicationAndUsage>
    <Description>Insulin aspart-fsan is a rapid-acting human insulin analog homologous with regular human insulin with the exception of a single substitution of the amino acid proline by aspartic acid in position B28, and is produced by recombinant DNA technology utilizing Escherichia coli. Insulin aspart-fsan has the empirical formula C256H381N65079S6 and a molecular weight of 5825.8 Da. Figure 1. Structural formula of insulin aspart-fsan. Garzulys (insulin aspart-fsan) injection is a sterile, clear, and colorless solution for subcutaneous or intravenous use. Each mL contains 100 units of insulin aspart-fsan and the inactive ingredients: dibasic sodium phosphate (0.997 mg), glycerin (16 mg), metacresol (1.72 mg), phenol (1.5 mg), sodium chloride (0.58 mg), zinc (19.6 mcg), and Water for Injection, USP. Garzulys has a pH of 7.2-7.6. Hydrochloric acid and/or sodium hydroxide may be added to adjust pH.</Description>
  </NDC>
  <NDC>
    <NDCCode>62864-662-01</NDCCode>
    <PackageDescription>47.31 mL in 1 BOTTLE (62864-662-01)</PackageDescription>
    <NDC11Code>62864-0662-01</NDC11Code>
    <ProductNDC>62864-662</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141023</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2015-12-18</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>62864-662-08</NDCCode>
    <PackageDescription>237 mL in 1 BOTTLE (62864-662-08)</PackageDescription>
    <NDC11Code>62864-0662-08</NDC11Code>
    <ProductNDC>62864-662</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141023</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-10-11</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62864-662-32</NDCCode>
    <PackageDescription>946 mL in 1 BOTTLE (62864-662-32)</PackageDescription>
    <NDC11Code>62864-0662-32</NDC11Code>
    <ProductNDC>62864-662</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20141023</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-10-11</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62864-665-08</NDCCode>
    <PackageDescription>237 mL in 1 BOTTLE (62864-665-08)</PackageDescription>
    <NDC11Code>62864-0665-08</NDC11Code>
    <ProductNDC>62864-665</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Truly Radiant</ProprietaryName>
    <ProprietaryNameSuffix>Whitening And Strengthening Rinse Clean And Fresh</ProprietaryNameSuffix>
    <NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151002</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part355</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>SODIUM FLUORIDE</SubstanceName>
    <StrengthNumber>.2</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Uses. Aids in the prevention of dental cavities.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-764-08</NDCCode>
    <PackageDescription>237 mL in 1 BOTTLE (62864-764-08) </PackageDescription>
    <NDC11Code>62864-0764-08</NDC11Code>
    <ProductNDC>62864-764</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Orajel Toothache Rinse</ProprietaryName>
    <NonProprietaryName>Benzyl Alcohol, Zinc Chloride</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20161201</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part356</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>BENZYL ALCOHOL; ZINC CHLORIDE</SubstanceName>
    <StrengthNumber>2.7; 1.5</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL</StrengthUnit>
    <Pharm_Classes>Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Pediculicide [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2023-01-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20221231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20181224</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Use for temporary relief of pain due to toothaches, minor irritation of the mouth and gums, occasional minor irritation, pain, sore mouth and sore throat.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-900-19</NDCCode>
    <PackageDescription>56 mL in 1 BOTTLE, WITH APPLICATOR (62864-900-19)</PackageDescription>
    <NDC11Code>62864-0900-19</NDC11Code>
    <ProductNDC>62864-900</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Ultramax Roll On</ProprietaryName>
    <ProprietaryNameSuffix>Antiperspirant Deodorant Powder Fresh</ProprietaryNameSuffix>
    <NonProprietaryName>Aluminum Zirconium Tetrachlorohydrex Gly</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20000728</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part350</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp</LabelerName>
    <SubstanceName>ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY</SubstanceName>
    <StrengthNumber>21</StrengthNumber>
    <StrengthUnit>g/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2015-12-25</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>62864-902-10</NDCCode>
    <PackageDescription>1 JAR in 1 CARTON (62864-902-10)  &gt; 28 g in 1 JAR</PackageDescription>
    <NDC11Code>62864-0902-10</NDC11Code>
    <ProductNDC>62864-902</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Arrid Extra Dry</ProprietaryName>
    <ProprietaryNameSuffix>Antiperspirant Deodorant</ProprietaryNameSuffix>
    <NonProprietaryName>Aluminum Sesquichlorohydrate 17%</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>19951108</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part350</ApplicationNumber>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>ALUMINUM SESQUICHLOROHYDRATE</SubstanceName>
    <StrengthNumber>170</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>reduces underarm perspiration.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62864-903-00</NDCCode>
    <PackageDescription>1 BOTTLE, PLASTIC in 1 CARTON (62864-903-00)  &gt; 125 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC</PackageDescription>
    <NDC11Code>62864-0903-00</NDC11Code>
    <ProductNDC>62864-903</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Baby Orajel Naturals</ProprietaryName>
    <ProprietaryNameSuffix>For Teething Pain Relief</ProprietaryNameSuffix>
    <NonProprietaryName>Calcarea Phosphorica, Coffea Cruda, Chamomilla</NonProprietaryName>
    <DosageFormName>TABLET, ORALLY DISINTEGRATING</DosageFormName>
    <RouteName>SUBLINGUAL</RouteName>
    <StartMarketingDate>20110615</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>TRIBASIC CALCIUM PHOSPHATE; ARABICA COFFEE BEAN; MATRICARIA RECUTITA</SubstanceName>
    <StrengthNumber>3; 3; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62864-903-12</NDCCode>
    <PackageDescription>1 BOTTLE, PLASTIC in 1 CARTON (62864-903-12)  &gt; 125 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC</PackageDescription>
    <NDC11Code>62864-0903-12</NDC11Code>
    <ProductNDC>62864-903</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Baby Orajel Naturals</ProprietaryName>
    <ProprietaryNameSuffix>For Teething Pain Relief</ProprietaryNameSuffix>
    <NonProprietaryName>Calcarea Phosphorica, Coffea Cruda, Chamomilla</NonProprietaryName>
    <DosageFormName>TABLET, ORALLY DISINTEGRATING</DosageFormName>
    <RouteName>SUBLINGUAL</RouteName>
    <StartMarketingDate>20110615</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Church &amp; Dwight Canada Corp.</LabelerName>
    <SubstanceName>TRIBASIC CALCIUM PHOSPHATE; ARABICA COFFEE BEAN; MATRICARIA RECUTITA</SubstanceName>
    <StrengthNumber>3; 3; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>62864-909-16</NDCCode><ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName><NonProprietaryName>Sodium Fluoride</NonProprietaryName></NDC><NDC><NDCCode>62864-662-16</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-665-16</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-759-16</NDCCode><ProprietaryName>Orajel Alcohol Free Antiseptic Rinse</ProprietaryName><NonProprietaryName>Hydrogen Peroxide 1.5%, Menthol 0.1%</NonProprietaryName></NDC><NDC><NDCCode>62864-760-16</NDCCode><ProprietaryName>Orajel Antiseptic Rinse</ProprietaryName><NonProprietaryName>Hydrogen Peroxide 1.5%, Menthol 0.1%</NonProprietaryName></NDC><NDC><NDCCode>62864-764-16</NDCCode><ProprietaryName>Orajel Toothache Rinse</ProprietaryName><NonProprietaryName>Benzyl Alcohol, Zinc Chloride</NonProprietaryName></NDC><NDC><NDCCode>62864-910-16</NDCCode><ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName><NonProprietaryName>Sodium Fluoride</NonProprietaryName></NDC><NDC><NDCCode>10237-909-16</NDCCode><ProprietaryName>Orajel Anticavity Fluoride Rinse</ProprietaryName><NonProprietaryName>Sodium Fluoride</NonProprietaryName></NDC><NDC><NDCCode>11084-909-16</NDCCode><ProprietaryName>Alcare Plus Foaming Antiseptic Handrub</ProprietaryName><NonProprietaryName>Alcohol</NonProprietaryName></NDC><NDC><NDCCode>12634-909-16</NDCCode><ProprietaryName>Promethazine Hydrochloride And Codeine Phosphate</ProprietaryName><NonProprietaryName>Promethazine Hydrochloride And Codeine Phosphate</NonProprietaryName></NDC><NDC><NDCCode>50474-909-16</NDCCode><ProprietaryName>Lortab</ProprietaryName><NonProprietaryName>Hydrocodone Bitartrate And Acetaminophen</NonProprietaryName></NDC><NDC><NDCCode>51414-909-16</NDCCode><ProprietaryName>Pain Relieving Burn Gel</ProprietaryName><NonProprietaryName>Burn Gel</NonProprietaryName></NDC><NDC><NDCCode>66651-909-16</NDCCode><NonProprietaryName>Memantine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>62864-901-25</NDCCode><ProprietaryName>Arrid Xx Roll On</ProprietaryName><NonProprietaryName>Aluminum Chlorohydrate</NonProprietaryName></NDC><NDC><NDCCode>14803-909-00</NDCCode><NonProprietaryName>Acetaminophen, Dextromethorphan Hydrobromide And Phenylephrine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>19515-909-52</NDCCode><ProprietaryName>Flulaval Quadrivalent</ProprietaryName><NonProprietaryName>Influenza Virus Vaccine</NonProprietaryName></NDC><NDC><NDCCode>49035-909-30</NDCCode><ProprietaryName>All Day Moisture</ProprietaryName><NonProprietaryName>Octinoxate, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>59735-909-02</NDCCode><ProprietaryName>Protectint 34c</ProprietaryName><NonProprietaryName>Homosalate, Octisalate, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>67254-909-01</NDCCode><NonProprietaryName>Lumefantrine</NonProprietaryName></NDC><NDC><NDCCode>69097-909-50</NDCCode><ProprietaryName>Leuprolide Acetate Depot</ProprietaryName><NonProprietaryName>Leuprolide Acetate</NonProprietaryName></NDC><NDC><NDCCode>71288-909-10</NDCCode><ProprietaryName>Insulin Diluting Medium For Garzulys</ProprietaryName><NonProprietaryName>Water Injection</NonProprietaryName></NDC><NDC><NDCCode>62864-662-01</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-662-08</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-662-32</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-665-08</NDCCode><ProprietaryName>Truly Radiant</ProprietaryName><NonProprietaryName>Sodium Fluoride 0.02%</NonProprietaryName></NDC><NDC><NDCCode>62864-764-08</NDCCode><ProprietaryName>Orajel Toothache Rinse</ProprietaryName><NonProprietaryName>Benzyl Alcohol, Zinc Chloride</NonProprietaryName></NDC><NDC><NDCCode>62864-900-19</NDCCode><ProprietaryName>Ultramax Roll On</ProprietaryName><NonProprietaryName>Aluminum Zirconium Tetrachlorohydrex Gly</NonProprietaryName></NDC><NDC><NDCCode>62864-902-10</NDCCode><ProprietaryName>Arrid Extra Dry</ProprietaryName><NonProprietaryName>Aluminum Sesquichlorohydrate 17%</NonProprietaryName></NDC><NDC><NDCCode>62864-903-00</NDCCode><ProprietaryName>Baby Orajel Naturals</ProprietaryName><NonProprietaryName>Calcarea Phosphorica, Coffea Cruda, Chamomilla</NonProprietaryName></NDC><NDC><NDCCode>62864-903-12</NDCCode><ProprietaryName>Baby Orajel Naturals</ProprietaryName><NonProprietaryName>Calcarea Phosphorica, Coffea Cruda, Chamomilla</NonProprietaryName></NDC></NDCList>
                    

Using REST to Invoke DataLabs API

Introduction

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

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

Working With DataLabs REST API

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

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

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

Four parameters are required with each “search” request:

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

Optional parameter:

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

All other query parameters (if any) are optional.

Full list of API parameters:

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

Operations Currently Available in the DataLabs REST API

Currently DataLabs RESTful Lookup Service supports following operations:

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

Plus there are three NPI-specific operations:

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

REST Search Examples

Query Parameter Reference

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

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

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

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

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

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

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

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

        Console.WriteLine(response);

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

            
{
  "NPI": [
    {
      "NPI": "1295783033",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "REDMOND EYE DOCTORS, PLLC",
      "FirstLineMailingAddress": "16375 NE 85TH ST",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3554",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-7363",
      "MailingAddressFaxNumber": "425-861-5585",
      "FirstLinePracticeLocationAddress": "16375 NE 85TH ST",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3554",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-7363",
      "PracticeLocationAddressFaxNumber": "425-861-5585",
      "EnumerationDate": "05/04/2006",
      "LastUpdateDate": "12/11/2007",
      "AuthorizedOfficialLastName": "MONTECILLO",
      "AuthorizedOfficialFirstName": "RANIA",
      "AuthorizedOfficialTitle": "OWNER",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "O.D.",
      "AuthorizedOfficialTelephoneNumber": "425-885-7363",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "801TX",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization."
    },
    {
      "NPI": "1346319878",
      "EntityType": "Organization",
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      "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",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "10/28/2024",
      "LastUpdateDate": "10/28/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "10/26/2024",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1912723131",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "WEIMER",
      "FirstName": "ALAYNA",
      "FirstLineMailingAddress": "2748 NW 19TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-7766",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-499-8292",
      "EnumerationDate": "12/03/2024",
      "LastUpdateDate": "12/03/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "171M00000X",
      "Taxonomy1": "Case Manager/Care Coordinator",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "12/03/2024",
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}
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