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How to Find 43948-1101-1 NDC Data Using DataLabs API

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{
  "NDC": [
    {
      "NDCCode": "43948-1101-1",
      "PackageDescription": "30 mL in 1 TUBE (43948-1101-1)",
      "NDC11Code": "43948-1101-01",
      "ProductNDC": "43948-1101",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr. Young 2p Pearl Brightening Balm Spf35 Pa",
      "NonProprietaryName": "Allantoin",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20120927",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctors Cosmetics Co., Ltd",
      "SubstanceName": "ALLANTOIN",
      "StrengthNumber": ".5",
      "StrengthUnit": "mg/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-1201-1",
      "PackageDescription": "15 mL in 1 TUBE (43948-1201-1)",
      "NDC11Code": "43948-1201-01",
      "ProductNDC": "43948-1201",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Ac Out Spot Stop Serum",
      "NonProprietaryName": "Salicylic Acid",
      "DosageFormName": "LIQUID",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20120927",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "The Doctors Cosmetics Co., Ltd",
      "SubstanceName": "SALICYLIC ACID",
      "StrengthNumber": ".1",
      "StrengthUnit": "mg/100mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "1.  On clean face, only apply on troubled areas. Do not rub.  2.  When applying on top of a make up, use tip of the tube."
    },
    {
      "NDCCode": "43948-1300-2",
      "PackageDescription": "1 TUBE in 1 CARTON (43948-1300-2)  > 30 mL in 1 TUBE (43948-1300-1) ",
      "NDC11Code": "43948-1300-02",
      "ProductNDC": "43948-1300",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Protect Prevent 2p Blemish Base",
      "NonProprietaryName": "Titanium Dioxide, Octinoxate, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE",
      "StrengthNumber": "2.67; 1.95; .27",
      "StrengthUnit": "g/30mL; g/30mL; g/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20171001",
      "SamplePackage": "N",
      "Description": "Uses: - Ultralight, pink toned beauty balm to protect, tint, and moisturize skin - Features SPF 35 PA++ sun protection. Directions: Apply moderate amount on entire face after basic skin care."
    },
    {
      "NDCCode": "43948-1310-2",
      "PackageDescription": "1 TUBE in 1 CARTON (43948-1310-2)  > 30 mL in 1 TUBE (43948-1310-1) ",
      "NDC11Code": "43948-1310-02",
      "ProductNDC": "43948-1310",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Protect Prevent 2p Pearl Brightening Balm",
      "NonProprietaryName": "Titanium Dioxide, Octinoxate, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE",
      "StrengthNumber": "2.67; 1.95; .27",
      "StrengthUnit": "g/30mL; g/30mL; g/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20171001",
      "SamplePackage": "N",
      "Description": "Uses: - Ultralight, dark toned beauty balm to protect, tint, and moisturize skin - Features SPF 35 PA++ sun protection. Directions: Apply moderate amount on entire face after basic skin care."
    },
    {
      "NDCCode": "43948-1320-2",
      "PackageDescription": "1 TUBE in 1 CARTON (43948-1320-2)  > 50 mL in 1 TUBE (43948-1320-1)",
      "NDC11Code": "43948-1320-02",
      "ProductNDC": "43948-1320",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Protect Prevent Uv Cut And Ultra Light Sun",
      "NonProprietaryName": "Octinoxate, Titanium Dioxide, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE",
      "StrengthNumber": "3; 2.5; .95",
      "StrengthUnit": "g/50mL; g/50mL; g/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2018-12-07",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "43948-1330-2",
      "PackageDescription": "1 TUBE in 1 CARTON (43948-1330-2)  > 30 mL in 1 TUBE (43948-1330-1)",
      "NDC11Code": "43948-1330-02",
      "ProductNDC": "43948-1330",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Protect Prevent Triple Action Bb",
      "NonProprietaryName": "Titanium Dioxide, Octinoxate",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "TITANIUM DIOXIDE; OCTINOXATE",
      "StrengthNumber": "2.4; 2.25",
      "StrengthUnit": "g/30mL; g/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "Description": "Uses: - Ultralight, Multifunctional beauty cream to protect, perfect, tint, and moisturize skin - Features SPF 33 PA+++ sun protection. Directions: Apply moderate amount on entire face after basic skin care."
    },
    {
      "NDCCode": "43948-1340-2",
      "PackageDescription": "1 TUBE in 1 CARTON (43948-1340-2)  > 15 mL in 1 TUBE (43948-1340-1) ",
      "NDC11Code": "43948-1340-02",
      "ProductNDC": "43948-1340",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Ac Control Ac Out Spot Stop Serum",
      "NonProprietaryName": "Salicylic Acid",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "SALICYLIC ACID",
      "StrengthNumber": ".01",
      "StrengthUnit": "g/15mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20171001",
      "SamplePackage": "N",
      "IndicationAndUsage": "Uses: Acne treatment spot serum containing green tea and white tea extracts soothes irritated area effectively. Ultralight transparent gel delivers reduced inflammation on contact."
    },
    {
      "NDCCode": "43948-1350-2",
      "PackageDescription": "1 BOTTLE, SPRAY in 1 CARTON (43948-1350-2)  > 140 mL in 1 BOTTLE, SPRAY (43948-1350-1) ",
      "NDC11Code": "43948-1350-02",
      "ProductNDC": "43948-1350",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young Ac Control U Line Clearing Mist",
      "NonProprietaryName": "Salicylic Acid",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20171001",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "Tdc, Co. Ltd",
      "SubstanceName": "SALICYLIC ACID",
      "StrengthNumber": ".14",
      "StrengthUnit": "g/140mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20171001",
      "SamplePackage": "N",
      "IndicationAndUsage": "Uses: A 360 acne treatment spray that works at any angle to fight breakouts wherever they occur. Spray even layer over affected areas."
    },
    {
      "NDCCode": "43948-3001-1",
      "PackageDescription": "10 mL in 1 BOTTLE, DROPPER (43948-3001-1)",
      "NDC11Code": "43948-3001-01",
      "ProductNDC": "43948-3001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr G Dewrinkle Booster Ample By Egf",
      "NonProprietaryName": "Adenosine Glycerin",
      "DosageFormName": "SOLUTION/ DROPS",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ADENOSINE; GLYCERIN",
      "StrengthNumber": ".04; .5",
      "StrengthUnit": "mL/10mL; mL/10mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-3002-1",
      "PackageDescription": "30 mL in 1 BOTTLE, PUMP (43948-3002-1)",
      "NDC11Code": "43948-3002-01",
      "ProductNDC": "43948-3002",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr G Dewrinkle Fortifier By Egf",
      "NonProprietaryName": "Adenosine Glycerin",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ADENOSINE; GLYCERIN",
      "StrengthNumber": ".012; 2.1",
      "StrengthUnit": "mL/30mL; mL/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-3003-1",
      "PackageDescription": "50 mL in 1 JAR (43948-3003-1)",
      "NDC11Code": "43948-3003-01",
      "ProductNDC": "43948-3003",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr G Dewrinkle Reformer By Egf",
      "NonProprietaryName": "Adenosine Dimethicone",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ADENOSINE; DIMETHICONE",
      "StrengthNumber": ".02; .35",
      "StrengthUnit": "mL/50mL; mL/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-4001-1",
      "PackageDescription": "30 mL in 1 BOTTLE, PUMP (43948-4001-1)",
      "NDC11Code": "43948-4001-01",
      "ProductNDC": "43948-4001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr G Whitening Fortifier By Egf",
      "NonProprietaryName": "Arbutin Glycerin",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ARBUTIN; GLYCERIN",
      "StrengthNumber": ".6; 3",
      "StrengthUnit": "mL/30mL; mL/30mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-4002-1",
      "PackageDescription": "50 mL in 1 JAR (43948-4002-1)",
      "NDC11Code": "43948-4002-01",
      "ProductNDC": "43948-4002",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr G Whitening Reformer By Egf",
      "NonProprietaryName": "Arbutin Dimethicone",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ARBUTIN; DIMETHICONE",
      "StrengthNumber": "1; 2",
      "StrengthUnit": "mL/50mL; mL/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-5001-1",
      "PackageDescription": "60 mL in 1 TUBE (43948-5001-1)",
      "NDC11Code": "43948-5001-01",
      "ProductNDC": "43948-5001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young 2p Blemish Base Spf35 Pa",
      "NonProprietaryName": "Allantoin",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ALLANTOIN",
      "StrengthNumber": "3.6",
      "StrengthUnit": "mL/60mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-5002-1",
      "PackageDescription": "50 mL in 1 TUBE (43948-5002-1)",
      "NDC11Code": "43948-5002-01",
      "ProductNDC": "43948-5002",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young 2p Brightening Uv Sun Block Spf50 Pa",
      "NonProprietaryName": "Arbutin",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ARBUTIN",
      "StrengthNumber": ".5",
      "StrengthUnit": "mL/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-5003-1",
      "PackageDescription": "50 mL in 1 TUBE (43948-5003-1)",
      "NDC11Code": "43948-5003-01",
      "ProductNDC": "43948-5003",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dr Young 2p Brightening Uv Sun Block Spf50 Pa",
      "NonProprietaryName": "Arbutin, Ethylhexyl Methoxycinnamate",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "ARBUTIN; OCTINOXATE",
      "StrengthNumber": ".5; 2.5",
      "StrengthUnit": "mL/50mL; mL/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-6001-1",
      "PackageDescription": "130 mL in 1 BOTTLE, SPRAY (43948-6001-1)",
      "NDC11Code": "43948-6001-01",
      "ProductNDC": "43948-6001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "High Protection Sun Air Spray Spf50 Pa",
      "NonProprietaryName": "Octinoxate Octisalate Aluminum Hydroxide",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "OCTINOXATE",
      "StrengthNumber": "9.75",
      "StrengthUnit": "mL/130mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-7001-1",
      "PackageDescription": "60 mL in 1 TUBE (43948-7001-1)",
      "NDC11Code": "43948-7001-01",
      "ProductNDC": "43948-7001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Hydra Intensive Blemish Balm Spf30 Pa",
      "NonProprietaryName": "Titanium Dioxide Octinoxate Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE",
      "StrengthNumber": "3; 1.8; .3",
      "StrengthUnit": "mL/60mL; mL/60mL; mL/60mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "43948-8001-1",
      "PackageDescription": "60 mL in 1 TUBE (43948-8001-1)",
      "NDC11Code": "43948-8001-01",
      "ProductNDC": "43948-8001",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Medi Uv Block Suncream Spf50 Pa",
      "NonProprietaryName": "Octinoxate Octocrylene",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20091101",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part352",
      "LabelerName": "The Doctor's Cosmetic Inc",
      "SubstanceName": "OCTINOXATE; OCTOCRYLENE",
      "StrengthNumber": "3; .6",
      "StrengthUnit": "mL/60mL; mL/60mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "0004-1101-50",
      "PackageDescription": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-1101-50) ",
      "NDC11Code": "00004-1101-50",
      "ProductNDC": "0004-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Xeloda",
      "NonProprietaryName": "Capecitabine",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "19980430",
      "EndMarketingDate": "20250731",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA020896",
      "LabelerName": "Genentech, Inc.",
      "SubstanceName": "CAPECITABINE",
      "StrengthNumber": "500",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2025-08-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "19980430",
      "EndMarketingDatePackage": "20250731",
      "SamplePackage": "N",
      "IndicationAndUsage": "XELODA (capecitabine) is a nucleoside metabolic inhibitor indicated for. Colorectal Cancer: 1 adjuvant treatment of patients with Stage III colon cancer as a single agent or as a component of a combination chemotherapy regimen. (1.1), 2 perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy. (1.1), 3 treatment of patients with unresectable or metastatic colorectal cancer as a single agent or as a component of a combination chemotherapy regimen. (1.1).",
      "Description": "Capecitabine is a nucleoside metabolic inhibitor. The chemical name is 5'-deoxy-5-fluoro-N-[(pentyloxy) carbonyl]-cytidine and has a molecular formula of C15H22FN3O6 and a molecular weight of 359.35. Capecitabine has the following structural formula. Capecitabine is a white to off-white crystalline powder with an aqueous solubility of 26 mg/mL at 20°C. XELODA (capecitabine) is supplied as biconvex, oblong film-coated tablets for oral use. Each light peach-colored tablet contains 150 mg capecitabine and each peach-colored tablet contains 500 mg capecitabine. The inactive ingredients in XELODA include: anhydrous lactose, croscarmellose sodium, hydroxypropyl methylcellulose, microcrystalline cellulose, magnesium stearate and purified water. The peach or light peach film coating contains hydroxypropyl methylcellulose, talc, titanium dioxide, and synthetic yellow and red iron oxides."
    },
    {
      "NDCCode": "0004-1101-75",
      "PackageDescription": "12 BLISTER PACK in 1 CARTON (0004-1101-75)  > 10 TABLET, FILM COATED in 1 BLISTER PACK",
      "NDC11Code": "00004-1101-75",
      "ProductNDC": "0004-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Xeloda",
      "NonProprietaryName": "Capecitabine",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "19980430",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA020896",
      "LabelerName": "Genentech, Inc.",
      "SubstanceName": "CAPECITABINE",
      "StrengthNumber": "500",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2017-01-02"
    },
    {
      "NDCCode": "0032-1101-01",
      "PackageDescription": "100 TABLET in 1 BOTTLE (0032-1101-01)",
      "NDC11Code": "00032-1101-01",
      "ProductNDC": "0032-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Aceon",
      "NonProprietaryName": "Perindopril Erbumine",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20101214",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA020184",
      "LabelerName": "Abbott Products, Inc.",
      "SubstanceName": "PERINDOPRIL ERBUMINE",
      "StrengthNumber": "2",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2014-11-28"
    },
    {
      "NDCCode": "0046-1101-81",
      "PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (0046-1101-81) ",
      "NDC11Code": "00046-1101-81",
      "ProductNDC": "0046-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Premarin",
      "NonProprietaryName": "Estrogens, Conjugated",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20060101",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA004782",
      "LabelerName": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.",
      "SubstanceName": "ESTROGENS, CONJUGATED",
      "StrengthNumber": ".45",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS]",
      "Status": "Active",
      "LastUpdate": "2026-06-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20060101",
      "SamplePackage": "N",
      "IndicationAndUsage": "PREMARIN is a mixture of estrogens indicated for: 1 Treatment of Moderate to Severe Vasomotor Symptoms due to Menopause (1.1) , 2 Treatment of Moderate to Severe Vulvar and Vaginal Atrophy due to Menopause (1.2) , 3 Treatment of Hypoestrogenism due to Hypogonadism, Castration or Primary Ovarian Failure (1.3) , 4 Treatment of Breast Cancer (for Palliation Only) in Appropriately Selected Women and Men with Metastatic Disease (1.4) , 5 Treatment of Advanced Androgen-Dependent Carcinoma of the Prostate (for Palliation Only) (1.5) , 6 Prevention of Postmenopausal Osteoporosis (1.6) .",
      "Description": "PREMARIN® (conjugated estrogens tablets, USP) for oral administration contains a mixture of CE purified from pregnant mares' urine and consists of the sodium salts of water-soluble estrogen sulfates blended to represent the average composition of material derived from pregnant mares' urine. It is a mixture of sodium estrone sulfate and sodium equilin sulfate. It contains concomitant components as sodium sulfate conjugates, 17α-dihydroequilin, 17α estradiol, and 17β-dihydroequilin. Tablets for oral administration are available in 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg strengths of CE. PREMARIN 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg tablets also contain the following inactive ingredients: calcium phosphate tribasic, carnauba wax, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, powdered cellulose, sucrose, and titanium dioxide. Each tablet strength contains the following colors:. PREMARIN tablets comply with USP Dissolution Test criteria, as outlined below."
    },
    {
      "NDCCode": "0069-1101-20",
      "PackageDescription": "5 BLISTER PACK in 1 CARTON (0069-1101-20)  / 1 KIT in 1 BLISTER PACK (0069-1101-04)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (0069-2085-02)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (0069-3085-01) ",
      "NDC11Code": "00069-1101-20",
      "ProductNDC": "0069-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Paxlovid",
      "NonProprietaryName": "Nirmatrelvir And Ritonavir",
      "DosageFormName": "KIT",
      "StartMarketingDate": "20220317",
      "MarketingCategoryName": "EMERGENCY USE AUTHORIZATION",
      "LabelerName": "Pfizer Laboratories Div Pfizer Inc",
      "Status": "Deprecated",
      "LastUpdate": "2024-03-12",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20220317",
      "SamplePackage": "N",
      "IndicationAndUsage": "The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for the emergency use of PAXLOVID for the treatment of adults and pediatric patients (12 years of age and older weighing at least 40 kg) with mild-to-moderate coronavirus disease 2019 (COVID-19) and who are at high riskDetermining whether a patient is at high risk for progression to severe COVID-19, including hospitalization or death, is based on the provider’s assessment of the individual patient being considered for treatment of COVID-19 and that patient’s medical history. For information on medical conditions and factors associated with increased risk for progression to severe COVID-19, see the Centers for Disease Control and Prevention (CDC) website: https://www.cdc.gov/coronavirus/2019-ncov/hcp/clinical-care/underlyingconditions.html. for progression to severe COVID-19, including hospitalization or death.",
      "Description": "PAXLOVID is nirmatrelvir tablets co-packaged with ritonavir tablets. Nirmatrelvir is a SARS-CoV-2 main protease (Mpro) inhibitor, and ritonavir is an HIV-1 protease inhibitor and CYP3A inhibitor."
    },
    {
      "NDCCode": "0121-1101-02",
      "PackageDescription": "10 VIAL, SINGLE-USE in 1 CARTON (0121-1101-02)  / 300 mg in 1 VIAL, SINGLE-USE (0121-1101-55) ",
      "NDC11Code": "00121-1101-02",
      "ProductNDC": "0121-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Pentamidine Isethionate",
      "NonProprietaryName": "Pentamidine Isethionate",
      "DosageFormName": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
      "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
      "StartMarketingDate": "20260612",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA206666",
      "LabelerName": "PAI Holdings, LLC dba PAI Pharma",
      "SubstanceName": "PENTAMIDINE DIISETHIONATE",
      "StrengthNumber": "300",
      "StrengthUnit": "mg/300mg",
      "Pharm_Classes": "Antiprotozoal [EPC]",
      "Status": "Active",
      "LastUpdate": "2026-06-13",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260612",
      "SamplePackage": "N",
      "IndicationAndUsage": "Pentamidine isethionate for injection is indicated for the treatment of pneumonia due to Pneumocystis carinii.",
      "Description": "Pentamidine isethionate for injection, an anti-protozoal agent, is a sterile, nonpyrogenic, lyophilized product.  After reconstitution, it should be administered by intramuscular (IM) or intravenous (IV) routes (see DOSAGE AND ADMINISTRATION).  Pentamidine isethionate is a white crystalline powder soluble in water and glycerin, slightly soluble in alcohol and insoluble in ether, acetone, and chloroform.  It is chemically designated as 4,4-[1,5-pentanediylbis(oxy)]bis-benzenecarboximidamid with the following structural formula. Each vial contains:Pentamidine isethionate . . . . . . . . . . . . . 300 mg."
    },
    {
      "NDCCode": "0187-1101-09",
      "PackageDescription": "20 g in 1 TUBE (0187-1101-09)",
      "NDC11Code": "00187-1101-09",
      "ProductNDC": "0187-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Tretinoin",
      "NonProprietaryName": "Tretinoin",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20090801",
      "EndMarketingDate": "20160531",
      "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
      "ApplicationNumber": "NDA022070",
      "LabelerName": "Valeant Pharmaceuticals North America LLC",
      "SubstanceName": "TRETINOIN",
      "StrengthNumber": ".05",
      "StrengthUnit": "g/100g",
      "Pharm_Classes": "Retinoid [EPC],Retinoids [Chemical/Ingredient]",
      "Status": "Deprecated",
      "LastUpdate": "2016-12-02"
    },
    {
      "NDCCode": "0187-1101-62",
      "PackageDescription": "2 g in 1 TUBE (0187-1101-62)",
      "NDC11Code": "00187-1101-62",
      "ProductNDC": "0187-1101",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Tretinoin",
      "NonProprietaryName": "Tretinoin",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20090801",
      "EndMarketingDate": "20160531",
      "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
      "ApplicationNumber": "NDA022070",
      "LabelerName": "Valeant Pharmaceuticals North America LLC",
      "SubstanceName": "TRETINOIN",
      "StrengthNumber": ".05",
      "StrengthUnit": "g/100g",
      "Pharm_Classes": "Retinoid [EPC],Retinoids [Chemical/Ingredient]",
      "Status": "Deprecated",
      "LastUpdate": "2016-12-02"
    },
    {
      "NDCCode": "0220-1101-11",
      "PackageDescription": "30 mL in 1 BOTTLE, GLASS (0220-1101-11)",
      "NDC11Code": "00220-1101-11",
      "ProductNDC": "0220-1101",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Calendula Officinalis Flowering Top",
      "DosageFormName": "PELLET",
      "StartMarketingDate": "20170101",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Laboratoires Boiron",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP",
      "StrengthNumber": "1",
      "StrengthUnit": "[hp_X]/mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "0220-1101-12",
      "PackageDescription": "60 mL in 1 BOTTLE, GLASS (0220-1101-12)",
      "NDC11Code": "00220-1101-12",
      "ProductNDC": "0220-1101",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Calendula Officinalis Flowering Top",
      "DosageFormName": "PELLET",
      "StartMarketingDate": "20170101",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Laboratoires Boiron",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP",
      "StrengthNumber": "1",
      "StrengthUnit": "[hp_X]/mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "0259-1101-20",
      "PackageDescription": "1 TUBE in 1 CARTON (0259-1101-20)  > 20 g in 1 TUBE",
      "NDC11Code": "00259-1101-20",
      "ProductNDC": "0259-1101",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Mederma For Kids",
      "NonProprietaryName": "Allantoin",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20140501",
      "EndMarketingDate": "20230831",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "Merz Pharmaceuticals, LLC",
      "SubstanceName": "ALLANTOIN",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/g",
      "Status": "Deprecated",
      "LastUpdate": "2023-09-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20140501",
      "EndMarketingDatePackage": "20230831",
      "SamplePackage": "N"
    }
  ]
}
                    
{"NDC":[{"NDCCode":"43948-1101-1","ProprietaryName":"Dr. Young 2p Pearl Brightening Balm Spf35 Pa","NonProprietaryName":"Allantoin"},{"NDCCode":"43948-1201-1","ProprietaryName":"Ac Out Spot Stop Serum","NonProprietaryName":"Salicylic Acid"},{"NDCCode":"43948-1300-2","ProprietaryName":"Dr Young Protect Prevent 2p Blemish Base","NonProprietaryName":"Titanium Dioxide, Octinoxate, Zinc Oxide"},{"NDCCode":"43948-1310-2","ProprietaryName":"Dr Young Protect Prevent 2p Pearl Brightening Balm","NonProprietaryName":"Titanium Dioxide, Octinoxate, Zinc Oxide"},{"NDCCode":"43948-1320-2","ProprietaryName":"Dr Young Protect Prevent Uv Cut And Ultra Light Sun","NonProprietaryName":"Octinoxate, Titanium Dioxide, Zinc Oxide"},{"NDCCode":"43948-1330-2","ProprietaryName":"Dr Young Protect Prevent Triple Action Bb","NonProprietaryName":"Titanium Dioxide, Octinoxate"},{"NDCCode":"43948-1340-2","ProprietaryName":"Dr Young Ac Control Ac Out Spot Stop Serum","NonProprietaryName":"Salicylic Acid"},{"NDCCode":"43948-1350-2","ProprietaryName":"Dr Young Ac Control U Line Clearing Mist","NonProprietaryName":"Salicylic Acid"},{"NDCCode":"43948-3001-1","ProprietaryName":"Dr G Dewrinkle Booster Ample By Egf","NonProprietaryName":"Adenosine Glycerin"},{"NDCCode":"43948-3002-1","ProprietaryName":"Dr G Dewrinkle Fortifier By Egf","NonProprietaryName":"Adenosine Glycerin"},{"NDCCode":"43948-3003-1","ProprietaryName":"Dr G Dewrinkle Reformer By Egf","NonProprietaryName":"Adenosine Dimethicone"},{"NDCCode":"43948-4001-1","ProprietaryName":"Dr G Whitening Fortifier By Egf","NonProprietaryName":"Arbutin Glycerin"},{"NDCCode":"43948-4002-1","ProprietaryName":"Dr G Whitening Reformer By Egf","NonProprietaryName":"Arbutin Dimethicone"},{"NDCCode":"43948-5001-1","ProprietaryName":"Dr Young 2p Blemish Base Spf35 Pa","NonProprietaryName":"Allantoin"},{"NDCCode":"43948-5002-1","ProprietaryName":"Dr Young 2p Brightening Uv Sun Block Spf50 Pa","NonProprietaryName":"Arbutin"},{"NDCCode":"43948-5003-1","ProprietaryName":"Dr Young 2p Brightening Uv Sun Block Spf50 Pa","NonProprietaryName":"Arbutin, Ethylhexyl Methoxycinnamate"},{"NDCCode":"43948-6001-1","ProprietaryName":"High Protection Sun Air Spray Spf50 Pa","NonProprietaryName":"Octinoxate Octisalate Aluminum Hydroxide"},{"NDCCode":"43948-7001-1","ProprietaryName":"Hydra Intensive Blemish Balm Spf30 Pa","NonProprietaryName":"Titanium Dioxide Octinoxate Zinc Oxide"},{"NDCCode":"43948-8001-1","ProprietaryName":"Medi Uv Block Suncream Spf50 Pa","NonProprietaryName":"Octinoxate Octocrylene"},{"NDCCode":"0004-1101-50","ProprietaryName":"Xeloda","NonProprietaryName":"Capecitabine"},{"NDCCode":"0004-1101-75","ProprietaryName":"Xeloda","NonProprietaryName":"Capecitabine"},{"NDCCode":"0032-1101-01","ProprietaryName":"Aceon","NonProprietaryName":"Perindopril Erbumine"},{"NDCCode":"0046-1101-81","ProprietaryName":"Premarin","NonProprietaryName":"Estrogens, Conjugated"},{"NDCCode":"0069-1101-20","ProprietaryName":"Paxlovid","NonProprietaryName":"Nirmatrelvir And Ritonavir"},{"NDCCode":"0121-1101-02","ProprietaryName":"Pentamidine Isethionate","NonProprietaryName":"Pentamidine Isethionate"},{"NDCCode":"0187-1101-09","ProprietaryName":"Tretinoin","NonProprietaryName":"Tretinoin"},{"NDCCode":"0187-1101-62","ProprietaryName":"Tretinoin","NonProprietaryName":"Tretinoin"},{"NDCCode":"0220-1101-11","NonProprietaryName":"Calendula Officinalis Flowering Top"},{"NDCCode":"0220-1101-12","NonProprietaryName":"Calendula Officinalis Flowering Top"},{"NDCCode":"0259-1101-20","ProprietaryName":"Mederma For Kids","NonProprietaryName":"Allantoin"}]}
                    
<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <NDC>
    <NDCCode>43948-1101-1</NDCCode>
    <PackageDescription>30 mL in 1 TUBE (43948-1101-1)</PackageDescription>
    <NDC11Code>43948-1101-01</NDC11Code>
    <ProductNDC>43948-1101</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr. Young 2p Pearl Brightening Balm Spf35 Pa</ProprietaryName>
    <NonProprietaryName>Allantoin</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20120927</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctors Cosmetics Co., Ltd</LabelerName>
    <SubstanceName>ALLANTOIN</SubstanceName>
    <StrengthNumber>.5</StrengthNumber>
    <StrengthUnit>mg/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-1201-1</NDCCode>
    <PackageDescription>15 mL in 1 TUBE (43948-1201-1)</PackageDescription>
    <NDC11Code>43948-1201-01</NDC11Code>
    <ProductNDC>43948-1201</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Ac Out Spot Stop Serum</ProprietaryName>
    <NonProprietaryName>Salicylic Acid</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20120927</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>The Doctors Cosmetics Co., Ltd</LabelerName>
    <SubstanceName>SALICYLIC ACID</SubstanceName>
    <StrengthNumber>.1</StrengthNumber>
    <StrengthUnit>mg/100mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>1.  On clean face, only apply on troubled areas. Do not rub.  2.  When applying on top of a make up, use tip of the tube.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>43948-1300-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (43948-1300-2)  &gt; 30 mL in 1 TUBE (43948-1300-1) </PackageDescription>
    <NDC11Code>43948-1300-02</NDC11Code>
    <ProductNDC>43948-1300</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Protect Prevent 2p Blemish Base</ProprietaryName>
    <NonProprietaryName>Titanium Dioxide, Octinoxate, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>2.67; 1.95; .27</StrengthNumber>
    <StrengthUnit>g/30mL; g/30mL; g/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171001</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <Description>Uses: - Ultralight, pink toned beauty balm to protect, tint, and moisturize skin - Features SPF 35 PA++ sun protection. Directions: Apply moderate amount on entire face after basic skin care.</Description>
  </NDC>
  <NDC>
    <NDCCode>43948-1310-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (43948-1310-2)  &gt; 30 mL in 1 TUBE (43948-1310-1) </PackageDescription>
    <NDC11Code>43948-1310-02</NDC11Code>
    <ProductNDC>43948-1310</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Protect Prevent 2p Pearl Brightening Balm</ProprietaryName>
    <NonProprietaryName>Titanium Dioxide, Octinoxate, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>2.67; 1.95; .27</StrengthNumber>
    <StrengthUnit>g/30mL; g/30mL; g/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171001</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <Description>Uses: - Ultralight, dark toned beauty balm to protect, tint, and moisturize skin - Features SPF 35 PA++ sun protection. Directions: Apply moderate amount on entire face after basic skin care.</Description>
  </NDC>
  <NDC>
    <NDCCode>43948-1320-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (43948-1320-2)  &gt; 50 mL in 1 TUBE (43948-1320-1)</PackageDescription>
    <NDC11Code>43948-1320-02</NDC11Code>
    <ProductNDC>43948-1320</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Protect Prevent Uv Cut And Ultra Light Sun</ProprietaryName>
    <NonProprietaryName>Octinoxate, Titanium Dioxide, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>3; 2.5; .95</StrengthNumber>
    <StrengthUnit>g/50mL; g/50mL; g/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2018-12-07</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-1330-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (43948-1330-2)  &gt; 30 mL in 1 TUBE (43948-1330-1)</PackageDescription>
    <NDC11Code>43948-1330-02</NDC11Code>
    <ProductNDC>43948-1330</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Protect Prevent Triple Action Bb</ProprietaryName>
    <NonProprietaryName>Titanium Dioxide, Octinoxate</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>TITANIUM DIOXIDE; OCTINOXATE</SubstanceName>
    <StrengthNumber>2.4; 2.25</StrengthNumber>
    <StrengthUnit>g/30mL; g/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <Description>Uses: - Ultralight, Multifunctional beauty cream to protect, perfect, tint, and moisturize skin - Features SPF 33 PA+++ sun protection. Directions: Apply moderate amount on entire face after basic skin care.</Description>
  </NDC>
  <NDC>
    <NDCCode>43948-1340-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (43948-1340-2)  &gt; 15 mL in 1 TUBE (43948-1340-1) </PackageDescription>
    <NDC11Code>43948-1340-02</NDC11Code>
    <ProductNDC>43948-1340</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Ac Control Ac Out Spot Stop Serum</ProprietaryName>
    <NonProprietaryName>Salicylic Acid</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>SALICYLIC ACID</SubstanceName>
    <StrengthNumber>.01</StrengthNumber>
    <StrengthUnit>g/15mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171001</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Uses: Acne treatment spot serum containing green tea and white tea extracts soothes irritated area effectively. Ultralight transparent gel delivers reduced inflammation on contact.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>43948-1350-2</NDCCode>
    <PackageDescription>1 BOTTLE, SPRAY in 1 CARTON (43948-1350-2)  &gt; 140 mL in 1 BOTTLE, SPRAY (43948-1350-1) </PackageDescription>
    <NDC11Code>43948-1350-02</NDC11Code>
    <ProductNDC>43948-1350</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young Ac Control U Line Clearing Mist</ProprietaryName>
    <NonProprietaryName>Salicylic Acid</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20171001</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>Tdc, Co. Ltd</LabelerName>
    <SubstanceName>SALICYLIC ACID</SubstanceName>
    <StrengthNumber>.14</StrengthNumber>
    <StrengthUnit>g/140mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171001</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Uses: A 360 acne treatment spray that works at any angle to fight breakouts wherever they occur. Spray even layer over affected areas.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>43948-3001-1</NDCCode>
    <PackageDescription>10 mL in 1 BOTTLE, DROPPER (43948-3001-1)</PackageDescription>
    <NDC11Code>43948-3001-01</NDC11Code>
    <ProductNDC>43948-3001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr G Dewrinkle Booster Ample By Egf</ProprietaryName>
    <NonProprietaryName>Adenosine Glycerin</NonProprietaryName>
    <DosageFormName>SOLUTION/ DROPS</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ADENOSINE; GLYCERIN</SubstanceName>
    <StrengthNumber>.04; .5</StrengthNumber>
    <StrengthUnit>mL/10mL; mL/10mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-3002-1</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, PUMP (43948-3002-1)</PackageDescription>
    <NDC11Code>43948-3002-01</NDC11Code>
    <ProductNDC>43948-3002</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr G Dewrinkle Fortifier By Egf</ProprietaryName>
    <NonProprietaryName>Adenosine Glycerin</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ADENOSINE; GLYCERIN</SubstanceName>
    <StrengthNumber>.012; 2.1</StrengthNumber>
    <StrengthUnit>mL/30mL; mL/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-3003-1</NDCCode>
    <PackageDescription>50 mL in 1 JAR (43948-3003-1)</PackageDescription>
    <NDC11Code>43948-3003-01</NDC11Code>
    <ProductNDC>43948-3003</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr G Dewrinkle Reformer By Egf</ProprietaryName>
    <NonProprietaryName>Adenosine Dimethicone</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ADENOSINE; DIMETHICONE</SubstanceName>
    <StrengthNumber>.02; .35</StrengthNumber>
    <StrengthUnit>mL/50mL; mL/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-4001-1</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, PUMP (43948-4001-1)</PackageDescription>
    <NDC11Code>43948-4001-01</NDC11Code>
    <ProductNDC>43948-4001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr G Whitening Fortifier By Egf</ProprietaryName>
    <NonProprietaryName>Arbutin Glycerin</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ARBUTIN; GLYCERIN</SubstanceName>
    <StrengthNumber>.6; 3</StrengthNumber>
    <StrengthUnit>mL/30mL; mL/30mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-4002-1</NDCCode>
    <PackageDescription>50 mL in 1 JAR (43948-4002-1)</PackageDescription>
    <NDC11Code>43948-4002-01</NDC11Code>
    <ProductNDC>43948-4002</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr G Whitening Reformer By Egf</ProprietaryName>
    <NonProprietaryName>Arbutin Dimethicone</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ARBUTIN; DIMETHICONE</SubstanceName>
    <StrengthNumber>1; 2</StrengthNumber>
    <StrengthUnit>mL/50mL; mL/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-5001-1</NDCCode>
    <PackageDescription>60 mL in 1 TUBE (43948-5001-1)</PackageDescription>
    <NDC11Code>43948-5001-01</NDC11Code>
    <ProductNDC>43948-5001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young 2p Blemish Base Spf35 Pa</ProprietaryName>
    <NonProprietaryName>Allantoin</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ALLANTOIN</SubstanceName>
    <StrengthNumber>3.6</StrengthNumber>
    <StrengthUnit>mL/60mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-5002-1</NDCCode>
    <PackageDescription>50 mL in 1 TUBE (43948-5002-1)</PackageDescription>
    <NDC11Code>43948-5002-01</NDC11Code>
    <ProductNDC>43948-5002</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young 2p Brightening Uv Sun Block Spf50 Pa</ProprietaryName>
    <NonProprietaryName>Arbutin</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ARBUTIN</SubstanceName>
    <StrengthNumber>.5</StrengthNumber>
    <StrengthUnit>mL/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-5003-1</NDCCode>
    <PackageDescription>50 mL in 1 TUBE (43948-5003-1)</PackageDescription>
    <NDC11Code>43948-5003-01</NDC11Code>
    <ProductNDC>43948-5003</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dr Young 2p Brightening Uv Sun Block Spf50 Pa</ProprietaryName>
    <NonProprietaryName>Arbutin, Ethylhexyl Methoxycinnamate</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>ARBUTIN; OCTINOXATE</SubstanceName>
    <StrengthNumber>.5; 2.5</StrengthNumber>
    <StrengthUnit>mL/50mL; mL/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-6001-1</NDCCode>
    <PackageDescription>130 mL in 1 BOTTLE, SPRAY (43948-6001-1)</PackageDescription>
    <NDC11Code>43948-6001-01</NDC11Code>
    <ProductNDC>43948-6001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>High Protection Sun Air Spray Spf50 Pa</ProprietaryName>
    <NonProprietaryName>Octinoxate Octisalate Aluminum Hydroxide</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>OCTINOXATE</SubstanceName>
    <StrengthNumber>9.75</StrengthNumber>
    <StrengthUnit>mL/130mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-7001-1</NDCCode>
    <PackageDescription>60 mL in 1 TUBE (43948-7001-1)</PackageDescription>
    <NDC11Code>43948-7001-01</NDC11Code>
    <ProductNDC>43948-7001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Hydra Intensive Blemish Balm Spf30 Pa</ProprietaryName>
    <NonProprietaryName>Titanium Dioxide Octinoxate Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>TITANIUM DIOXIDE; OCTINOXATE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>3; 1.8; .3</StrengthNumber>
    <StrengthUnit>mL/60mL; mL/60mL; mL/60mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>43948-8001-1</NDCCode>
    <PackageDescription>60 mL in 1 TUBE (43948-8001-1)</PackageDescription>
    <NDC11Code>43948-8001-01</NDC11Code>
    <ProductNDC>43948-8001</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Medi Uv Block Suncream Spf50 Pa</ProprietaryName>
    <NonProprietaryName>Octinoxate Octocrylene</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20091101</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part352</ApplicationNumber>
    <LabelerName>The Doctor's Cosmetic Inc</LabelerName>
    <SubstanceName>OCTINOXATE; OCTOCRYLENE</SubstanceName>
    <StrengthNumber>3; .6</StrengthNumber>
    <StrengthUnit>mL/60mL; mL/60mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>0004-1101-50</NDCCode>
    <PackageDescription>120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0004-1101-50) </PackageDescription>
    <NDC11Code>00004-1101-50</NDC11Code>
    <ProductNDC>0004-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Xeloda</ProprietaryName>
    <NonProprietaryName>Capecitabine</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19980430</StartMarketingDate>
    <EndMarketingDate>20250731</EndMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA020896</ApplicationNumber>
    <LabelerName>Genentech, Inc.</LabelerName>
    <SubstanceName>CAPECITABINE</SubstanceName>
    <StrengthNumber>500</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2025-08-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>19980430</StartMarketingDatePackage>
    <EndMarketingDatePackage>20250731</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>XELODA (capecitabine) is a nucleoside metabolic inhibitor indicated for. Colorectal Cancer: 1 adjuvant treatment of patients with Stage III colon cancer as a single agent or as a component of a combination chemotherapy regimen. (1.1), 2 perioperative treatment of adults with locally advanced rectal cancer as a component of chemoradiotherapy. (1.1), 3 treatment of patients with unresectable or metastatic colorectal cancer as a single agent or as a component of a combination chemotherapy regimen. (1.1).</IndicationAndUsage>
    <Description>Capecitabine is a nucleoside metabolic inhibitor. The chemical name is 5'-deoxy-5-fluoro-N-[(pentyloxy) carbonyl]-cytidine and has a molecular formula of C15H22FN3O6 and a molecular weight of 359.35. Capecitabine has the following structural formula. Capecitabine is a white to off-white crystalline powder with an aqueous solubility of 26 mg/mL at 20°C. XELODA (capecitabine) is supplied as biconvex, oblong film-coated tablets for oral use. Each light peach-colored tablet contains 150 mg capecitabine and each peach-colored tablet contains 500 mg capecitabine. The inactive ingredients in XELODA include: anhydrous lactose, croscarmellose sodium, hydroxypropyl methylcellulose, microcrystalline cellulose, magnesium stearate and purified water. The peach or light peach film coating contains hydroxypropyl methylcellulose, talc, titanium dioxide, and synthetic yellow and red iron oxides.</Description>
  </NDC>
  <NDC>
    <NDCCode>0004-1101-75</NDCCode>
    <PackageDescription>12 BLISTER PACK in 1 CARTON (0004-1101-75)  &gt; 10 TABLET, FILM COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>00004-1101-75</NDC11Code>
    <ProductNDC>0004-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Xeloda</ProprietaryName>
    <NonProprietaryName>Capecitabine</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19980430</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA020896</ApplicationNumber>
    <LabelerName>Genentech, Inc.</LabelerName>
    <SubstanceName>CAPECITABINE</SubstanceName>
    <StrengthNumber>500</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2017-01-02</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0032-1101-01</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (0032-1101-01)</PackageDescription>
    <NDC11Code>00032-1101-01</NDC11Code>
    <ProductNDC>0032-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Aceon</ProprietaryName>
    <NonProprietaryName>Perindopril Erbumine</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20101214</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA020184</ApplicationNumber>
    <LabelerName>Abbott Products, Inc.</LabelerName>
    <SubstanceName>PERINDOPRIL ERBUMINE</SubstanceName>
    <StrengthNumber>2</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-11-28</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0046-1101-81</NDCCode>
    <PackageDescription>100 TABLET, FILM COATED in 1 BOTTLE (0046-1101-81) </PackageDescription>
    <NDC11Code>00046-1101-81</NDC11Code>
    <ProductNDC>0046-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Premarin</ProprietaryName>
    <NonProprietaryName>Estrogens, Conjugated</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20060101</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA004782</ApplicationNumber>
    <LabelerName>Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.</LabelerName>
    <SubstanceName>ESTROGENS, CONJUGATED</SubstanceName>
    <StrengthNumber>.45</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-06-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20060101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>PREMARIN is a mixture of estrogens indicated for: 1 Treatment of Moderate to Severe Vasomotor Symptoms due to Menopause (1.1) , 2 Treatment of Moderate to Severe Vulvar and Vaginal Atrophy due to Menopause (1.2) , 3 Treatment of Hypoestrogenism due to Hypogonadism, Castration or Primary Ovarian Failure (1.3) , 4 Treatment of Breast Cancer (for Palliation Only) in Appropriately Selected Women and Men with Metastatic Disease (1.4) , 5 Treatment of Advanced Androgen-Dependent Carcinoma of the Prostate (for Palliation Only) (1.5) , 6 Prevention of Postmenopausal Osteoporosis (1.6) .</IndicationAndUsage>
    <Description>PREMARIN® (conjugated estrogens tablets, USP) for oral administration contains a mixture of CE purified from pregnant mares' urine and consists of the sodium salts of water-soluble estrogen sulfates blended to represent the average composition of material derived from pregnant mares' urine. It is a mixture of sodium estrone sulfate and sodium equilin sulfate. It contains concomitant components as sodium sulfate conjugates, 17α-dihydroequilin, 17α estradiol, and 17β-dihydroequilin. Tablets for oral administration are available in 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg strengths of CE. PREMARIN 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg tablets also contain the following inactive ingredients: calcium phosphate tribasic, carnauba wax, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, powdered cellulose, sucrose, and titanium dioxide. Each tablet strength contains the following colors:. PREMARIN tablets comply with USP Dissolution Test criteria, as outlined below.</Description>
  </NDC>
  <NDC>
    <NDCCode>0069-1101-20</NDCCode>
    <PackageDescription>5 BLISTER PACK in 1 CARTON (0069-1101-20)  / 1 KIT in 1 BLISTER PACK (0069-1101-04)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (0069-2085-02)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (0069-3085-01) </PackageDescription>
    <NDC11Code>00069-1101-20</NDC11Code>
    <ProductNDC>0069-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Paxlovid</ProprietaryName>
    <NonProprietaryName>Nirmatrelvir And Ritonavir</NonProprietaryName>
    <DosageFormName>KIT</DosageFormName>
    <StartMarketingDate>20220317</StartMarketingDate>
    <MarketingCategoryName>EMERGENCY USE AUTHORIZATION</MarketingCategoryName>
    <LabelerName>Pfizer Laboratories Div Pfizer Inc</LabelerName>
    <Status>Deprecated</Status>
    <LastUpdate>2024-03-12</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220317</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for the emergency use of PAXLOVID for the treatment of adults and pediatric patients (12 years of age and older weighing at least 40 kg) with mild-to-moderate coronavirus disease 2019 (COVID-19) and who are at high riskDetermining whether a patient is at high risk for progression to severe COVID-19, including hospitalization or death, is based on the provider’s assessment of the individual patient being considered for treatment of COVID-19 and that patient’s medical history. For information on medical conditions and factors associated with increased risk for progression to severe COVID-19, see the Centers for Disease Control and Prevention (CDC) website: https://www.cdc.gov/coronavirus/2019-ncov/hcp/clinical-care/underlyingconditions.html. for progression to severe COVID-19, including hospitalization or death.</IndicationAndUsage>
    <Description>PAXLOVID is nirmatrelvir tablets co-packaged with ritonavir tablets. Nirmatrelvir is a SARS-CoV-2 main protease (Mpro) inhibitor, and ritonavir is an HIV-1 protease inhibitor and CYP3A inhibitor.</Description>
  </NDC>
  <NDC>
    <NDCCode>0121-1101-02</NDCCode>
    <PackageDescription>10 VIAL, SINGLE-USE in 1 CARTON (0121-1101-02)  / 300 mg in 1 VIAL, SINGLE-USE (0121-1101-55) </PackageDescription>
    <NDC11Code>00121-1101-02</NDC11Code>
    <ProductNDC>0121-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Pentamidine Isethionate</ProprietaryName>
    <NonProprietaryName>Pentamidine Isethionate</NonProprietaryName>
    <DosageFormName>INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION</DosageFormName>
    <RouteName>INTRAMUSCULAR; INTRAVENOUS</RouteName>
    <StartMarketingDate>20260612</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA206666</ApplicationNumber>
    <LabelerName>PAI Holdings, LLC dba PAI Pharma</LabelerName>
    <SubstanceName>PENTAMIDINE DIISETHIONATE</SubstanceName>
    <StrengthNumber>300</StrengthNumber>
    <StrengthUnit>mg/300mg</StrengthUnit>
    <Pharm_Classes>Antiprotozoal [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-06-13</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260612</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Pentamidine isethionate for injection is indicated for the treatment of pneumonia due to Pneumocystis carinii.</IndicationAndUsage>
    <Description>Pentamidine isethionate for injection, an anti-protozoal agent, is a sterile, nonpyrogenic, lyophilized product.  After reconstitution, it should be administered by intramuscular (IM) or intravenous (IV) routes (see DOSAGE AND ADMINISTRATION).  Pentamidine isethionate is a white crystalline powder soluble in water and glycerin, slightly soluble in alcohol and insoluble in ether, acetone, and chloroform.  It is chemically designated as 4,4-[1,5-pentanediylbis(oxy)]bis-benzenecarboximidamid with the following structural formula. Each vial contains:Pentamidine isethionate . . . . . . . . . . . . . 300 mg.</Description>
  </NDC>
  <NDC>
    <NDCCode>0187-1101-09</NDCCode>
    <PackageDescription>20 g in 1 TUBE (0187-1101-09)</PackageDescription>
    <NDC11Code>00187-1101-09</NDC11Code>
    <ProductNDC>0187-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Tretinoin</ProprietaryName>
    <NonProprietaryName>Tretinoin</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20090801</StartMarketingDate>
    <EndMarketingDate>20160531</EndMarketingDate>
    <MarketingCategoryName>NDA AUTHORIZED GENERIC</MarketingCategoryName>
    <ApplicationNumber>NDA022070</ApplicationNumber>
    <LabelerName>Valeant Pharmaceuticals North America LLC</LabelerName>
    <SubstanceName>TRETINOIN</SubstanceName>
    <StrengthNumber>.05</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Pharm_Classes>Retinoid [EPC],Retinoids [Chemical/Ingredient]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2016-12-02</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0187-1101-62</NDCCode>
    <PackageDescription>2 g in 1 TUBE (0187-1101-62)</PackageDescription>
    <NDC11Code>00187-1101-62</NDC11Code>
    <ProductNDC>0187-1101</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Tretinoin</ProprietaryName>
    <NonProprietaryName>Tretinoin</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20090801</StartMarketingDate>
    <EndMarketingDate>20160531</EndMarketingDate>
    <MarketingCategoryName>NDA AUTHORIZED GENERIC</MarketingCategoryName>
    <ApplicationNumber>NDA022070</ApplicationNumber>
    <LabelerName>Valeant Pharmaceuticals North America LLC</LabelerName>
    <SubstanceName>TRETINOIN</SubstanceName>
    <StrengthNumber>.05</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Pharm_Classes>Retinoid [EPC],Retinoids [Chemical/Ingredient]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2016-12-02</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0220-1101-11</NDCCode>
    <PackageDescription>30 mL in 1 BOTTLE, GLASS (0220-1101-11)</PackageDescription>
    <NDC11Code>00220-1101-11</NDC11Code>
    <ProductNDC>0220-1101</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Calendula Officinalis Flowering Top</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <StartMarketingDate>20170101</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Laboratoires Boiron</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWERING TOP</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>[hp_X]/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>0220-1101-12</NDCCode>
    <PackageDescription>60 mL in 1 BOTTLE, GLASS (0220-1101-12)</PackageDescription>
    <NDC11Code>00220-1101-12</NDC11Code>
    <ProductNDC>0220-1101</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Calendula Officinalis Flowering Top</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <StartMarketingDate>20170101</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Laboratoires Boiron</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWERING TOP</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>[hp_X]/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>0259-1101-20</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (0259-1101-20)  &gt; 20 g in 1 TUBE</PackageDescription>
    <NDC11Code>00259-1101-20</NDC11Code>
    <ProductNDC>0259-1101</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Mederma For Kids</ProprietaryName>
    <NonProprietaryName>Allantoin</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20140501</StartMarketingDate>
    <EndMarketingDate>20230831</EndMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>Merz Pharmaceuticals, LLC</LabelerName>
    <SubstanceName>ALLANTOIN</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2023-09-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20140501</StartMarketingDatePackage>
    <EndMarketingDatePackage>20230831</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
</NDCList>
                    
<NDCList><NDC><NDCCode>43948-1101-1</NDCCode><ProprietaryName>Dr. Young 2p Pearl Brightening Balm Spf35 Pa</ProprietaryName><NonProprietaryName>Allantoin</NonProprietaryName></NDC><NDC><NDCCode>43948-1201-1</NDCCode><ProprietaryName>Ac Out Spot Stop Serum</ProprietaryName><NonProprietaryName>Salicylic Acid</NonProprietaryName></NDC><NDC><NDCCode>43948-1300-2</NDCCode><ProprietaryName>Dr Young Protect Prevent 2p Blemish Base</ProprietaryName><NonProprietaryName>Titanium Dioxide, Octinoxate, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>43948-1310-2</NDCCode><ProprietaryName>Dr Young Protect Prevent 2p Pearl Brightening Balm</ProprietaryName><NonProprietaryName>Titanium Dioxide, Octinoxate, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>43948-1320-2</NDCCode><ProprietaryName>Dr Young Protect Prevent Uv Cut And Ultra Light Sun</ProprietaryName><NonProprietaryName>Octinoxate, Titanium Dioxide, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>43948-1330-2</NDCCode><ProprietaryName>Dr Young Protect Prevent Triple Action Bb</ProprietaryName><NonProprietaryName>Titanium Dioxide, Octinoxate</NonProprietaryName></NDC><NDC><NDCCode>43948-1340-2</NDCCode><ProprietaryName>Dr Young Ac Control Ac Out Spot Stop Serum</ProprietaryName><NonProprietaryName>Salicylic Acid</NonProprietaryName></NDC><NDC><NDCCode>43948-1350-2</NDCCode><ProprietaryName>Dr Young Ac Control U Line Clearing Mist</ProprietaryName><NonProprietaryName>Salicylic Acid</NonProprietaryName></NDC><NDC><NDCCode>43948-3001-1</NDCCode><ProprietaryName>Dr G Dewrinkle Booster Ample By Egf</ProprietaryName><NonProprietaryName>Adenosine Glycerin</NonProprietaryName></NDC><NDC><NDCCode>43948-3002-1</NDCCode><ProprietaryName>Dr G Dewrinkle Fortifier By Egf</ProprietaryName><NonProprietaryName>Adenosine Glycerin</NonProprietaryName></NDC><NDC><NDCCode>43948-3003-1</NDCCode><ProprietaryName>Dr G Dewrinkle Reformer By Egf</ProprietaryName><NonProprietaryName>Adenosine Dimethicone</NonProprietaryName></NDC><NDC><NDCCode>43948-4001-1</NDCCode><ProprietaryName>Dr G Whitening Fortifier By Egf</ProprietaryName><NonProprietaryName>Arbutin Glycerin</NonProprietaryName></NDC><NDC><NDCCode>43948-4002-1</NDCCode><ProprietaryName>Dr G Whitening Reformer By Egf</ProprietaryName><NonProprietaryName>Arbutin Dimethicone</NonProprietaryName></NDC><NDC><NDCCode>43948-5001-1</NDCCode><ProprietaryName>Dr Young 2p Blemish Base Spf35 Pa</ProprietaryName><NonProprietaryName>Allantoin</NonProprietaryName></NDC><NDC><NDCCode>43948-5002-1</NDCCode><ProprietaryName>Dr Young 2p Brightening Uv Sun Block Spf50 Pa</ProprietaryName><NonProprietaryName>Arbutin</NonProprietaryName></NDC><NDC><NDCCode>43948-5003-1</NDCCode><ProprietaryName>Dr Young 2p Brightening Uv Sun Block Spf50 Pa</ProprietaryName><NonProprietaryName>Arbutin, Ethylhexyl Methoxycinnamate</NonProprietaryName></NDC><NDC><NDCCode>43948-6001-1</NDCCode><ProprietaryName>High Protection Sun Air Spray Spf50 Pa</ProprietaryName><NonProprietaryName>Octinoxate Octisalate Aluminum Hydroxide</NonProprietaryName></NDC><NDC><NDCCode>43948-7001-1</NDCCode><ProprietaryName>Hydra Intensive Blemish Balm Spf30 Pa</ProprietaryName><NonProprietaryName>Titanium Dioxide Octinoxate Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>43948-8001-1</NDCCode><ProprietaryName>Medi Uv Block Suncream Spf50 Pa</ProprietaryName><NonProprietaryName>Octinoxate Octocrylene</NonProprietaryName></NDC><NDC><NDCCode>0004-1101-50</NDCCode><ProprietaryName>Xeloda</ProprietaryName><NonProprietaryName>Capecitabine</NonProprietaryName></NDC><NDC><NDCCode>0004-1101-75</NDCCode><ProprietaryName>Xeloda</ProprietaryName><NonProprietaryName>Capecitabine</NonProprietaryName></NDC><NDC><NDCCode>0032-1101-01</NDCCode><ProprietaryName>Aceon</ProprietaryName><NonProprietaryName>Perindopril Erbumine</NonProprietaryName></NDC><NDC><NDCCode>0046-1101-81</NDCCode><ProprietaryName>Premarin</ProprietaryName><NonProprietaryName>Estrogens, Conjugated</NonProprietaryName></NDC><NDC><NDCCode>0069-1101-20</NDCCode><ProprietaryName>Paxlovid</ProprietaryName><NonProprietaryName>Nirmatrelvir And Ritonavir</NonProprietaryName></NDC><NDC><NDCCode>0121-1101-02</NDCCode><ProprietaryName>Pentamidine Isethionate</ProprietaryName><NonProprietaryName>Pentamidine Isethionate</NonProprietaryName></NDC><NDC><NDCCode>0187-1101-09</NDCCode><ProprietaryName>Tretinoin</ProprietaryName><NonProprietaryName>Tretinoin</NonProprietaryName></NDC><NDC><NDCCode>0187-1101-62</NDCCode><ProprietaryName>Tretinoin</ProprietaryName><NonProprietaryName>Tretinoin</NonProprietaryName></NDC><NDC><NDCCode>0220-1101-11</NDCCode><NonProprietaryName>Calendula Officinalis Flowering Top</NonProprietaryName></NDC><NDC><NDCCode>0220-1101-12</NDCCode><NonProprietaryName>Calendula Officinalis Flowering Top</NonProprietaryName></NDC><NDC><NDCCode>0259-1101-20</NDCCode><ProprietaryName>Mederma For Kids</ProprietaryName><NonProprietaryName>Allantoin</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.

Parameter Meaning Notes
domain Domain
  • Currently following data domains are supported:
    • NPI - NPI Number Lookup
    • HCPCS - Healthcare Provider Procedure Coding System Lookup
    • NDC - National Drug Code Lookup
    • NDCA - Animal Drug Product Listing Directory Lookup
    • CLIA - Clinical Laboratory Improvement Amendments
    • HPTC - Healthcare Provider Taxonomy Code Lookup
    • NAICS - North American Industry Classification System Lookup
    • LOINC - Logical Observation Identifiers Names and Codes (LOINC®) Lookup
    • DRG - Diagnosis-Related Group Lookup
    • ICD9 - Ninth Revision of the International Classification of Diseases Lookup
    • ICD10 - Tenth Revision of the International Classification of Diseases Lookup
    • ICD10DRUGS - ICD-10-CM Table Of Drugs And Chemicals Lookup
    • ZIP - Postal Codes used by the United States Postal Service
operation Operation
  • Generic operations:
    • check_status - this method allows to get current code status.
    • search - allows retrieval of set of items (up to 30) 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.
    • 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.
  • 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.
q Query
  • The search expression. May vary depending on the operation.
    • Free form text like: “q=blood glucose monitor” (search operation)
    • Exact code value : “q=1285636522” (getcode operation)
    • List of codes : “q=1285636522,1730198755,1427145176,1487730636” (getcodes operation)
zipcode Query for NPI by Zip code/radius Lookup
  • The search expression for zip code.
    • Exact code value : “zipcode=98052” (search operation)
radius Query for NPI by Zip code/radius Lookup
  • The search expression for radius.
    • Exact code value : “radius=20” (search operation)
fromdate Query for Deactivated NPI
  • The search expression for fromdate.
    • Exact code value : “fromdate=05/01/2023” (search operation - format MM/DD/YYYY)
todate Query for Deactivated NPI
  • The search expression for tomdate.
    • Exact code value : “todate=05/31/2023” (search operation - format MM/DD/YYYY)
tin Query for IRS Lookup
  • The search expression for tin number.
    • Exact code value : “tin=942404110” (search operation)
tinname Query for IRS Lookup
  • The search expression for tin name.
    • Free form text like: “tinname=apple inc.” (search operation)
rt Data format
  • If you don't specify an rt parameter, the API returns data in the JSON format. This is equivalent to rt=json.
  • Accepted values are:
    • json
    • minjson (minified json)
    • xml
    • minxml (minified xml)
token Your API key
num Number of search results to return
  • You can specify the how many results to return for the current search.
  • Valid values are integers between 1 and 100, inclusive.
  • If num is not used, a value of 30 is assumed.
friendlyprint Returns a response with indentations and line breaks
  • If friendlyprint is not used, a “true” value is assumed. This is equivalent to friendlyprint=true.
  • Accepted values are:
    • true - the results returned by the server will be more “human readable”.
    • false - the results returned by the server will not have indentations and line breaks.
ICD9/ICD10 Parameters
codeType Specifies whether ICD code is "dx"(Diagnosis) or "pcs"(Procedure).
  • Required for ICD only.
  • If you don't specify an codeType parameter this is equivalent to codeType=dx.
  • Accepted values are:
    • dx (diagnosis)
    • pcs (procedure)
qf Specifies predicate in form of tuple "qf=City:true:Phoenix".
  • Expected to be one or many "qf" parameters in request.
  • Required for following operations:
    • validate
    • paginate_with_predicates
    • search_with_predicates
  • Tuple values are (order based):
    • NPI Field Name
      • NPI
      • Phone
      • Fax
      • FirstName
      • LastName
      • OrganizationName
      • OtherOrganizationName
      • Address1
      • Address2
      • Zip
      • City
      • State
      • IndividualOrganizationCode
    • Exact Match
      • true
      • false
    • Expected Field Value
orderField Sort order field name
  • Expected to be one "orderField" parameter in request.
  • Required for following operations:
    • paginate_with_predicates
  • Values are:
    • NPI
    • Phone
    • Fax
    • FirstName
    • LastName
    • OrganizationName
    • OtherOrganizationName
    • Address1
    • Address2
    • Zip
    • City
    • State
    • IndividualOrganizationCode
pageNo Page Number
  • Ordinal page number.
  • Required for following operations:
    • paginate_with_predicates
    • zipradius
    • npideactivated
pageSize Page Size
  • Expected page size.
  • Required for following operations:
    • paginate_with_predicates

DataLabs Coding Library - Quering NPI Registry - REST API Examples

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();
    }
}
            
        

Output

            
{
  "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.",
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      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

Full Text Search Fundamentals

Facts

Everybody uses full text search. Full-text search is the most common technique used in search engines. The amount of information has just become too much to access it using navigation and categories alone. Full-text search reduces the hassle of searching for a keyword in huge amounts of metadata, such as the World Wide Web and commercial-scale databases. Full-text search became popular in late 1990s, when the Internet and Big Data began to became a part of everyday life.

How does it work

Users only provide keywords and expect the search engine to provide good results. Relevancy of documents is expected to be good and users want the results they are looking to be present in the top ten. How relevant a document is search engine decides based on scientifically proven algorithms. Besides getting the best results the user wants to be supported during the search process. Features like suggestions and highlighting on the result excerpt can help with this.

Full Text Search & DataLabs REST API

DataLabs REST API allows you to search the full text of healthcare providers database (NPI Registry). To find the information you need and make your search easy, please use our REST API for automation, or visit our NPI Lookup page for manual search ( NPI Number Lookup). We are still improving and enhancing Full Text NPI Search based on users feedbacks. Please email your comments and suggestions for improvement using our feedback page.

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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
{
  "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",
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}
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