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How to Find 24330-111-85 NDC Data Using DataLabs API

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{
  "NDC": [
    {
      "NDCCode": "24330-111-85",
      "PackageDescription": "89 mL in 1 CAN (24330-111-85)",
      "NDC11Code": "24330-0111-85",
      "ProductNDC": "24330-111",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "First Degree Burn",
      "NonProprietaryName": "Benzocaine, Triclosan",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130201",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "The Akshay Wellness Group, Inc.",
      "SubstanceName": "BENZOCAINE; TRICLOSAN",
      "StrengthNumber": "200; 1.3",
      "StrengthUnit": "mg/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2020-01-01",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "IndicationAndUsage": "for temporary relief of pain and itching from minor burns, cuts and scrapes. first aid to help prevent infection in minor burns, cuts and scrapes."
    },
    {
      "NDCCode": "21130-111-85",
      "PackageDescription": "1 BOTTLE in 1 CARTON (21130-111-85)  / 250 TABLET in 1 BOTTLE",
      "NDC11Code": "21130-0111-85",
      "ProductNDC": "21130-111",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Signature Care Pain Relief",
      "NonProprietaryName": "Acetaminophen",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150901",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M013",
      "LabelerName": "Safeway",
      "SubstanceName": "ACETAMINOPHEN",
      "StrengthNumber": "500",
      "StrengthUnit": "mg/1",
      "Status": "Active",
      "LastUpdate": "2024-09-24",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20150901",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily relieves minor aches and pains due to:. the common cold. headache. backache. minor pain of arthritis. toothache. muscular aches. premenstrual and menstrual cramps. temporarily reduces fever."
    },
    {
      "NDCCode": "21922-111-15",
      "PackageDescription": "1 TUBE in 1 CARTON (21922-111-15)  / 85 g in 1 TUBE",
      "NDC11Code": "21922-0111-15",
      "ProductNDC": "21922-111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Econazole Nitrate",
      "NonProprietaryName": "Econazole Nitrate",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20260701",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA076574",
      "LabelerName": "Encube Ethicals, Inc.",
      "SubstanceName": "ECONAZOLE NITRATE",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/g",
      "Pharm_Classes": "Azole Antifungal [EPC], Azoles [CS]",
      "Status": "Active",
      "LastUpdate": "2026-07-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260701",
      "SamplePackage": "N",
      "IndicationAndUsage": "Econazole nitrate cream is indicated for topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, Microsporum canis, Microsporum audouini, Microsporum gypseum, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis, and in the treatment of tinea versicolor.",
      "Description": "Econazole nitrate cream contains the antifungal agent, econazole nitrate 1% in a water-miscible base consisting of pegoxol 7 stearate, peglicol 5 oleate, mineral oil, benzoic acid, butylated hydroxyanisole, and purified water. The white to off-white soft cream is for topical use only. Chemically, econazole nitrate is 1-[2-{(4-chloro-phenyl) methoxy}-2-(2, 4-dichlorophenyl) ethyl]-1H-imidazole mononitrate. Its structure is as follows."
    },
    {
      "NDCCode": "42783-111-85",
      "PackageDescription": "12 CARTON in 1 CASE (42783-111-85)  > 1 TUBE in 1 CARTON > 85 g in 1 TUBE",
      "NDC11Code": "42783-0111-85",
      "ProductNDC": "42783-111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Zithranol",
      "NonProprietaryName": "Anthralin",
      "DosageFormName": "SHAMPOO",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20120305",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "Elorac Inc.",
      "SubstanceName": "ANTHRALIN",
      "StrengthNumber": "1",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Zithranol Shampoo for the treatment of scalp psoriasis in subjects 12 years of age and older (see PRECAUTIONS). Patients should be instructed to use Zithranol Shampoo for the minimum time period necessary to achieve the desired results.",
      "Description": "Zithranol Shampoo contains 1% anthralin in a shampoo base containing glyceryl monolaurate, glyceryl monomyristate, citric acid, sodium hydroxide, FD&C Blue No. 1, Macare® G-2C, and purified water. The chemical name of anthralin is 1,8-dihydroxy-9-anthrone and its structural formula is."
    },
    {
      "NDCCode": "43744-111-85",
      "PackageDescription": "25000 g in 1 DRUM (43744-111-85)",
      "NDC11Code": "43744-0111-85",
      "ProductNDC": "43744-111",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Bumetanide",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20110707",
      "EndMarketingDate": "20130624",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "CBSCHEM LIMITED",
      "SubstanceName": "BUMETANIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/g",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20130624"
    },
    {
      "NDCCode": "58607-111-85",
      "PackageDescription": "100 BLISTER PACK in 1 BOX (58607-111-85)  > 10 CAPSULE in 1 BLISTER PACK",
      "NDC11Code": "58607-0111-85",
      "ProductNDC": "58607-111",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Myferon 150",
      "NonProprietaryName": "Iron Sucrose",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "19961201",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "MARTIN EKWEALOR PHARMACEUTICALS, INC.",
      "SubstanceName": "IRON SUCROSE",
      "StrengthNumber": "150",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Myferon 150 is indicated for the prevention and treatment of iron deficiency anemia and/or nutritional megaloblastic anemias.",
      "Description": "Myferon 150, Polysaccharide Iron Complex capsules are a preparation of ferric Iron complexed to a low molecular weight polysaccharide. This polysaccharide is obtained by extensive hydrolysis of starch. Myferon 150 is a dark brown powder that when dissolved in water, forms a very dark brown solution. As an organic complex, polysaccharide iron contains no free iron. It is tasteless, odorless and readily soluble in water."
    },
    {
      "NDCCode": "69949-111-01",
      "PackageDescription": "85 g in 1 TUBE (69949-111-01) ",
      "NDC11Code": "69949-0111-01",
      "ProductNDC": "69949-111",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Mineral Body Sunscreen Unscented",
      "NonProprietaryName": "Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20230801",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M020",
      "LabelerName": "Synchronicity Spa, Inc. DBA Suntegrity",
      "SubstanceName": "ZINC OXIDE",
      "StrengthNumber": "200",
      "StrengthUnit": "mg/g",
      "Status": "Active",
      "LastUpdate": "2023-12-14",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230801",
      "SamplePackage": "N",
      "IndicationAndUsage": "helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases risk of skin cancer and early skin aging caused by the sun."
    },
    {
      "NDCCode": "80587-111-03",
      "PackageDescription": "85 g in 1 BOTTLE (80587-111-03) ",
      "NDC11Code": "80587-0111-03",
      "ProductNDC": "80587-111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Urea Cream 40%",
      "NonProprietaryName": "Urea Cream 40%",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20211118",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "Prime Labs, LLC dba Quality CDMO",
      "SubstanceName": "UREA",
      "StrengthNumber": "400",
      "StrengthUnit": "mg/g",
      "Status": "Deprecated",
      "LastUpdate": "2022-06-25",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20231231",
      "StartMarketingDatePackage": "20211118",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "82699-111-02",
      "PackageDescription": "85 g in 1 CANISTER (82699-111-02) ",
      "NDC11Code": "82699-0111-02",
      "ProductNDC": "82699-111",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Right Guard Sport Antiperspirant Deodorant Gel Cool",
      "NonProprietaryName": "Right Guard Sport Antiperspirant Deodorant Gel Cool",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20241017",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M019",
      "LabelerName": "Thriving Brands LLC",
      "SubstanceName": "ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY",
      "StrengthNumber": "16.4",
      "StrengthUnit": "g/100g",
      "Status": "Active",
      "LastUpdate": "2026-01-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20241017",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "17156-021-01",
      "PackageDescription": "1 VIAL in 1 BOX (17156-021-01)  / 1 mL in 1 VIAL",
      "NDC11Code": "17156-0021-01",
      "ProductNDC": "17156-021",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Indium In 111 Oxyquinoline",
      "NonProprietaryName": "Indium In-111 Oxyquinoline",
      "DosageFormName": "SOLUTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "19851201",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA019044",
      "LabelerName": "Medi-Physics Inc. dba GE Healthcare.",
      "SubstanceName": "INDIUM IN-111 OXYQUINOLINE",
      "StrengthNumber": "1",
      "StrengthUnit": "ug/mL",
      "Status": "Active",
      "LastUpdate": "2024-01-12",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "19851201",
      "SamplePackage": "N",
      "IndicationAndUsage": "Indium In 111 Oxyquinoline Solution is indicated for radiolabeling autologous leukocytes. Indium In 111 oxyquinoline labeled leukocytes may be used as an adjunct in the detection of inflammatory processes to which leukocytes migrate, such as those associated with abscesses or other infection, following reinjection and detection by appropriate imaging procedures. The degree of accuracy may vary with labeling techniques and with the size, location and nature of the inflammatory process. Indium In 111 oxyquinoline labeled leukocyte imaging is not the preferred technique for the initial evaluation of patients with a high clinical probability of an abscess in a known location. Ultrasound or computed tomography may provide a better anatomical delineation of the infectious process and information may be obtained more quickly than with labeled leukocytes. If localization by these techniques is successful, labeled leukocytes should not be used as a confirmatory procedure. If localization or diagnosis by these methods fails or is ambiguous, indium In 111 oxyquinoline labeled leukocyte imaging may be appropriate.",
      "Description": "Indium In 111 Oxyquinoline (oxine) Solution is a diagnostic radiopharmaceutical intended for radiolabeling autologous leukocytes. It is supplied as a sterile, non-pyrogenic, isotonic aqueous solution with a pH range of 6.5 to 7.5 [sodium hydroxide and hydrochloric acid may be used to adjust the pH]. Each mL of the solution contains 37 MBq, 1 mCi of indium In 111 [no carrier added, >1.85 GBq/mcg indium (>50 mCi/mcg indium)] at calibration time, 50 mcg oxyquinoline, 100 mcg polysorbate 80, and 6 mg of HEPES (N-2-hydroxyethyl-piperazine-N'-2-ethane sulfonic acid) buffer in 0.75% Sodium Chloride Solution. The drug is intended to be used as a single-dose vial and contains no bacteriostatic agent. The radionuclidic impurity limit for indium 114m is not greater than 37 kBq, 1 µCi of indium 114m per 37 MBq, 1 mCi of indium In 111 at the time of calibration. The radionuclidic composition at expiration time is not less than 99.75% of indium In 111 and not more than 0.25% of indium In 114m/114. Chemical name: Indium In 111 Oxyquinoline. The precise structure of the indium In 111 oxyquinoline complex is unknown at this time. The empirical formula is (C9H6NO)3 In 111."
    },
    {
      "NDCCode": "54288-111-05",
      "PackageDescription": "5 VIAL in 1 CARTON (54288-111-05)  / 1 mL in 1 VIAL (54288-111-01) ",
      "NDC11Code": "54288-0111-05",
      "ProductNDC": "54288-111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Hyoscyamine Sulfate",
      "NonProprietaryName": "Hyoscyamine Sulfate",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "SUBCUTANEOUS",
      "StartMarketingDate": "20191018",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "BPI Labs LLC",
      "SubstanceName": "HYOSCYAMINE SULFATE",
      "StrengthNumber": ".5",
      "StrengthUnit": "mg/mL",
      "Status": "Active",
      "LastUpdate": "2025-12-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20191018",
      "SamplePackage": "N",
      "IndicationAndUsage": "Hyoscyamine sulfate Injection, USP is effective as adjunctive therapy in the treatment of peptic ulcer. In acute episodes, Hyoscyamine sulfate Injection, USP can be used to control gastric secretion, visceral spasm and hypermotility in spastic colitis, spastic bladder, cystitis, pylorospasm, and associated abdominal cramps. For use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and functional gastrointestinal disorders. Also as adjunctive therapy in the treatment of neurogenic bladder and neurogenic bowel disturbances (including the splenic flexure syndrome and neurogenic colon). Parenterally administered Hyoscyamine sulfate Injection, USP is also effective in reducing gastrointestinal motility to facilitate diagnostic procedures such as endoscopy or hypotonic duodenography. Hyoscyamine sulfate Injection, USP may be used to reduce pain and hypersecretion in pancreatitis, in certain cases of partial heart block associated with vagal activity, and as an antidote for poisoning by anticholinesterase agents. In Anesthesia. Hyoscyamine sulfate Injection, USP is indicated as a pre-operative antimuscarinic to reduce salivary, tracheobronchial, and pharyngeal secretions, to reduce the volume and acidity of gastric secretions, and to block cardiac vagal inhibitory reflexes during induction of anesthesia and intubation. Hyoscyamine sulfate Injection, USP protects against the peripheral muscarinic effects such as bradycardia and excessive secretions produced by halogenated hydrocarbons and cholinergic agents such as physostigmine, neostigmine, and pyridostigmine given to reverse the actions of curariform agents. In Urology. Hyoscyamine sulfate Injection, USP may also be used intravenously to improve radiologic visibility of the kidneys. It is also indicated along with morphine or other narcotics in symptomatic relief of biliary and renal colic.",
      "Description": "Hyoscyamine sulfate injection, USP is a sterile solution containing 0.5 mg hyoscyamine sulfate per mL in water for injection. Hyoscyamine sulfate Injection, USP is one of the principal anticholinergic/antispasmodic components of belladonna alkaloids. The empirical formula is (C 17H 23NO 3) 2H 2SO 42H 20 and the molecular weight is 712.85. Chemically, it is benzeneacetic acid, α-(hydroxymethyl)-,8-methyl-8-azabicyclo [3.2.1.] oct-3-yl ester, [3(S)-endo]-, sulfate (2:1), dihydrate with the following structure. The 1 mL vials contain as inactive ingredients: water for injection, pH is adjusted with hydrochloric acid when necessary."
    },
    {
      "NDCCode": "59310-111-06",
      "PackageDescription": "1 POUCH in 1 CARTON (59310-111-06)  / 1 INHALER in 1 POUCH / 1 POWDER, METERED in 1 INHALER",
      "NDC11Code": "59310-0111-06",
      "ProductNDC": "59310-111",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Airduo Digihaler",
      "NonProprietaryName": "Fluticasone Propionate And Salmeterol",
      "DosageFormName": "POWDER, METERED",
      "RouteName": "RESPIRATORY (INHALATION)",
      "StartMarketingDate": "20200915",
      "EndMarketingDate": "20240831",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA208799",
      "LabelerName": "Teva Respiratory, LLC",
      "SubstanceName": "FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE",
      "StrengthNumber": "55; 14",
      "StrengthUnit": "ug/1; ug/1",
      "Pharm_Classes": "Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2024-09-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20200915",
      "EndMarketingDatePackage": "20240831",
      "SamplePackage": "N",
      "IndicationAndUsage": "AirDuo® Digihaler® is indicated for the treatment of asthma in adult and pediatric patients aged 12 years and older. AirDuo Digihaler should be used for patients not adequately controlled on a long term asthma control medication such as an inhaled corticosteroid or whose disease warrants initiation of treatment with both an inhaled corticosteroid and long acting beta2-adrenergic agonist (LABA). Limitations of Use:. AirDuo Digihaler is not indicated for the relief of acute bronchospasm.",
      "Description": "AirDuo Digihaler 55/14 mcg, AirDuo Digihaler 113/14 mcg and AirDuo Digihaler 232/14 mcg are combinations of fluticasone propionate and salmeterol. Fluticasone Propionate. One active component of AirDuo Digihaler is fluticasone propionate, a corticosteroid having the chemical name S-(fluoromethyl) 6α,9-difluoro-11ß,17-dihydroxy-16α-methyl-3-oxoandrosta-1,4-diene-17ß-carbothioate, 17-propionate, and the following chemical structure. Fluticasone propionate is a white powder with a molecular weight of 500.6, and the empirical formula is C25H31F3O5S. It is practically insoluble in water, freely soluble in dimethyl sulfoxide and dimethylformamide, and slightly soluble in methanol and 95% ethanol. Salmeterol Xinafoate. The other active component of AirDuo Digihaler is salmeterol xinafoate, a beta2–adrenergic bronchodilator. Salmeterol xinafoate is the racemic form of the 1‑hydroxy‑2‑naphthoic acid salt of salmeterol. It has the chemical name 4-hydroxy-α -[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-1,3-benzenedimethanol, 1-hydroxy-2-naphthalenecarboxylate and the following chemical structure. Salmeterol xinafoate is a white powder with a molecular weight of 603.8, and the empirical formula is C25H37NO4C11H8O3. It is freely soluble in methanol; slightly soluble in ethanol, chloroform, and isopropanol; and sparingly soluble in water. AirDuo Digihaler. AirDuo Digihaler is a multidose dry powder inhaler (MDPI) with an electronic module, for oral inhalation only. It contains fluticasone propionate, salmeterol xinafoate, and lactose monohydrate (which may contain milk proteins). The opening of the mouthpiece cover meters 5.5 mg of the formulation from the device reservoir, which contains 55 mcg, 113 mcg, or 232 mcg of fluticasone propionate, and 14 mcg of salmeterol base (equivalent to 20.3 mcg of salmeterol xinafoate). Patient inhalation through the mouthpiece causes the deagglomeration and aerosolization of the drug particles as the formulation moves through the cyclone component of the device. This is followed by dispersion into the airstream. Under standardized in vitro test conditions, the AirDuo Digihaler inhaler delivers 49 mcg, 100 mcg, or 202 mcg of fluticasone propionate and 12.75 mcg of salmeterol base (equivalent to 18.5 mcg of salmeterol xinafoate), with lactose from the mouthpiece when tested at a flow rate of 85 L/min for 1.4 seconds. The amount of drug delivered to the lung will depend on patient factors such as inspiratory flow profiles. In adult subjects (N=50, aged 18 to 45 years) with asthma, mean peak inspiratory flow (PIF) through the MDPI was 108.28 L/min (range: 70.37 to 129.24 L/min). In adolescent subjects (N=50, aged 12 to 17 years) with asthma, mean peak inspiratory flow (PIF) through the MDPI was 106.72 L/min (range: 73.64 to 125.51 L/min). AirDuo Digihaler includes a QR code (on the top of the inhaler), and contains a built-in electronic module which automatically detects, records and stores data on inhaler events, including peak inspiratory flow rate (L/min). AirDuo Digihaler may pair with and transmit data to the mobile App where inhaler events are categorized."
    },
    {
      "NDCCode": "69945-132-06",
      "PackageDescription": "1 VIAL, GLASS in 1 CAN (69945-132-06)  > .5 mL in 1 VIAL, GLASS",
      "NDC11Code": "69945-0132-06",
      "ProductNDC": "69945-132",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Indium In 111 Chloride",
      "NonProprietaryName": "Indium In 111 Chloride",
      "DosageFormName": "SOLUTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20071207",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA019841",
      "LabelerName": "Curium US LLC",
      "SubstanceName": "INDIUM CHLORIDE IN-111",
      "StrengthNumber": "10",
      "StrengthUnit": "mCi/mL",
      "Status": "Deprecated",
      "LastUpdate": "2024-09-24",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20071207",
      "SamplePackage": "N",
      "IndicationAndUsage": "Indium In 111 Chloride Sterile Solution is indicated for radiolabeling ProstaScint preparations used for in vivo diagnostic imaging procedures. It is also indicated for radiolabeling Zevalin preparations used for Radioimmunotherapy procedures. Please refer to the package insert for ProstaScint or Zevalin for information on the final drug product.",
      "Description": "Indium In 111 Chloride Sterile Solution is indicated for radiolabeling ProstaScint preparations used for in vivo diagnostic imaging procedures. It is also indicated for radiolabeling Zevalin preparations used for Radioimmunotherapy procedures. It is supplied as a sterile, non-pyrogenic solution of Indium In 111 Chloride in 0.05 molar hydrochloric acid. No carrier has been added to the solution. Each 0.5 milliliter of the solution contains 185 megabequerels (5 millicuries) of Indium In 111 Chloride at time of calibration (specific activity of >1.85 GBq/μg Indium; >50 mCi/μg Indium at this time of calibration). The solution pH is 1.1 to 1.4."
    },
    {
      "NDCCode": "72536-0920-1",
      "PackageDescription": "1 mL in 1 VIAL, SINGLE-DOSE (72536-0920-1) ",
      "NDC11Code": "72536-0920-01",
      "ProductNDC": "72536-0920",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Indium In 111 Oxyquinoline",
      "NonProprietaryName": "Indium In-111 Oxyquinoline",
      "DosageFormName": "LIQUID",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20190927",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA202586",
      "LabelerName": "BWXT Medical Ltd.",
      "SubstanceName": "INDIUM IN-111 OXYQUINOLINE",
      "StrengthNumber": "1",
      "StrengthUnit": "mCi/mL",
      "Status": "Active",
      "LastUpdate": "2024-11-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20190927",
      "SamplePackage": "N",
      "IndicationAndUsage": "Indium In 111 oxyquinoline is indicated for radiolabeling autologous leukocytes. Indium In 111 oxyquinoline labeled leukocytes may be used as an adjunct in the detection of inflammatory processes to which leukocytes migrate, such as those associated with abscesses or other infection, following reinjection and detection by appropriate imaging procedures. The degree of accuracy may vary with labeling techniques and with the size, location and nature of the inflammatory process. Indium In 111 oxyquinoline labeled leukocyte imaging is not the preferred technique for the initial evaluation of patients with a high clinical probability of an abscess in a known location. Ultrasound or computed tomography may provide a better anatomical delineation of the infectious process and information may be obtained more quickly than with labeled leukocytes. If localization by these techniques is successful, labeled leukocytes should not be used as a confirmatory procedure. If localization or diagnosis by these methods fails or is ambiguous, indium In 111 oxyquinoline labeled leukocyte imaging may be appropriate.",
      "Description": "Indium In 111 oxyquinoline (oxine) is a diagnostic radiopharmaceutical intended for radiolabeling autologous leukocytes. It is supplied as a sterile, non-pyrogenic, isotonic aqueous solution with a pH range of 6.5 to 7.5. Each mL of the solution contains 37 MBq, 1 mCi of indium In 111 [no carrier added, >1.85 GBq/µg indium (>50 mCi/µg indium)] at calibration time, 50 µg oxyquinoline, 100 µg polysorbate 80, and 6 mg of HEPES (N-2-hydroxyethyl-piperazine-N’-2-ethane sulfonic acid) buffer in 0.75% sodium chloride solution. The drug is intended for single use only and contains no bacteriostatic agent. The radionuclidic impurity limit for indium 114m is not greater than 37 kBq, 1 µCi of indium 114m per 37 MBq, 1 mCi of indium In 111 at the time of calibration. The radionuclidic composition at expiration time is not less than 99.75% of indium In 111 and not more than 0.25% of indium In 114m/114. Chemical name: Indium In 111 Oxyquinoline. The precise structure of the indium In 111 oxyquinoline complex is unknown at this time. The empirical formula is (C9H6NO)3 In 111."
    },
    {
      "NDCCode": "76229-123-01",
      "PackageDescription": "1 BOTTLE in 1 PACKAGE (76229-123-01)  / 85 mL in 1 BOTTLE",
      "NDC11Code": "76229-0123-01",
      "ProductNDC": "76229-123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Likewise Hand Moisturizer - Sun Protectant Spf 50",
      "NonProprietaryName": "Octinoxate, Octisalate, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20110620",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M020",
      "LabelerName": "Likewise Incorporated",
      "SubstanceName": "OCTINOXATE; OCTISALATE; ZINC OXIDE",
      "StrengthNumber": "75; 50; 111.6",
      "StrengthUnit": "mg/mL; mg/mL; mg/mL",
      "Status": "Active",
      "LastUpdate": "2023-12-18",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20171219",
      "SamplePackage": "N",
      "IndicationAndUsage": "Helps prevent sunburn. Higher SPF provides more protection. Retains SPF after 40 minutes of activity in water or vigorous sweating.",
      "Description": "protect hydrate renew  . . . . . . .   NORMAL TO DRY SKIN  Daily moisturizer + Sunscreen  Dermatologist developed  Calms and softens dry, irritated skin with Niacinamide  Anti-aging antioxidants reverse daily damage and rejuvenate skin  Contains Vitamins B, C and E and Natural Soy to improve skin tone and texture  Works wonders as a nighttime moisturizer, too Non-greasy light coverage (apply 1 pea-size drop)  Delightfully fragrance free  . . . . . . .  LikewiseSkinCare.com  LIKEWISE INCORPORATED  200 COOL SPRINGS BOULEVARD  FRANKLIN, TENNESSEE 37067  IN CASE OF ADVERSE REACTION: 877.778.9546."
    },
    {
      "NDCCode": "24330-110-14",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-110-14)  > 14 g in 1 TUBE",
      "NDC11Code": "24330-0110-14",
      "ProductNDC": "24330-110",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "First Degree",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "TINCTURE",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Active",
      "LastUpdate": "2015-08-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20140501",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds."
    },
    {
      "NDCCode": "24330-110-21",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-110-21)  > 21 g in 1 TUBE",
      "NDC11Code": "24330-0110-21",
      "ProductNDC": "24330-110",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "First Degree",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "TINCTURE",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Active",
      "LastUpdate": "2015-08-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20070101",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds."
    },
    {
      "NDCCode": "24330-110-22",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-110-22)  > 21 g in 1 TUBE",
      "NDC11Code": "24330-0110-22",
      "ProductNDC": "24330-110",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "First Degree",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "TINCTURE",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Active",
      "LastUpdate": "2015-08-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20150301",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds."
    },
    {
      "NDCCode": "24330-130-02",
      "PackageDescription": "1 TUBE in 1 BOX (24330-130-02)  > 21 g in 1 TUBE",
      "NDC11Code": "24330-0130-02",
      "ProductNDC": "24330-130",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "First Degree Maximum Strength Burn",
      "NonProprietaryName": "Pramoxine Hydrochloride",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20170309",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "PRAMOXINE HYDROCHLORIDE",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/g",
      "Status": "Active",
      "LastUpdate": "2017-04-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20170309",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of pain and itching associated with: 1 minor burns, 2 insect bites, 3 sunburns, 4 minor cuts, 5 scrapes, 6 minor skin irritations."
    },
    {
      "NDCCode": "24330-210-01",
      "PackageDescription": "1 TUBE in 1 POUCH (24330-210-01)  > 7.1 g in 1 TUBE",
      "NDC11Code": "24330-0210-01",
      "ProductNDC": "24330-210",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunburnt",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "TINCTURE",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Deprecated",
      "LastUpdate": "2018-04-09",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "24330-210-03",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-210-03)  > 71 g in 1 TUBE",
      "NDC11Code": "24330-0210-03",
      "ProductNDC": "24330-210",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunburnt Advanced After-sun",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Active",
      "LastUpdate": "2018-04-09",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20160901",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves symptoms of mild and moderate sunburn such as: 1 overheated skin, 2 redness, 3 rawness, 4 itching, 5 dryness."
    },
    {
      "NDCCode": "24330-210-06",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-210-06)  > 170 g in 1 TUBE",
      "NDC11Code": "24330-0210-06",
      "ProductNDC": "24330-210",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunburnt Advanced After-sun",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Active",
      "LastUpdate": "2018-04-09",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20160901",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves symptoms of mild and moderate sunburn such as: 1 overheated skin, 2 redness, 3 rawness, 4 itching, 5 dryness."
    },
    {
      "NDCCode": "24330-210-21",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-210-21)  > 21.3 g in 1 TUBE",
      "NDC11Code": "24330-0210-21",
      "ProductNDC": "24330-210",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunburnt",
      "NonProprietaryName": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
      "DosageFormName": "TINCTURE",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20070101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
      "StrengthNumber": "1; 1; 3",
      "StrengthUnit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
      "Status": "Deprecated",
      "LastUpdate": "2018-04-09",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "24330-240-01",
      "PackageDescription": "1 TUBE in 1 CARTON (24330-240-01)  > 142 g in 1 TUBE",
      "NDC11Code": "24330-0240-01",
      "ProductNDC": "24330-240",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Sunburnt Plus Pain Relief",
      "NonProprietaryName": "Lidocaine Hydrochloride",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20180315",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "Welmedix LLC dba Welmedix Consumer Healthcare",
      "SubstanceName": "LIDOCAINE HYDROCHLORIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/100g",
      "Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]",
      "Status": "Active",
      "LastUpdate": "2018-03-15",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20180315",
      "SamplePackage": "N",
      "IndicationAndUsage": "Temporarily relieves pain and itching due to: 1 sunburn, 2 minor burns, 3 insect bites, 4 minor skin irritations, 5 minor cuts, 6 scrapes."
    },
    {
      "NDCCode": "24330-410-06",
      "PackageDescription": "57 g in 1 TUBE (24330-410-06)",
      "NDC11Code": "24330-0410-06",
      "ProductNDC": "24330-410",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro Extra Strength Rapid Rash Relief",
      "NonProprietaryName": "Petrolatum, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130401",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "Welmedix Llc",
      "SubstanceName": "PETROLATUM; ZINC OXIDE",
      "StrengthNumber": "49; 15",
      "StrengthUnit": "g/100g; g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "24330-410-07",
      "PackageDescription": "113 g in 1 TUBE (24330-410-07) ",
      "NDC11Code": "24330-0410-07",
      "ProductNDC": "24330-410",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro Extra Strength Rapid Rash Relief",
      "NonProprietaryName": "Petrolatum, Zinc Oxide",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130401",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M012",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "PETROLATUM; ZINC OXIDE",
      "StrengthNumber": "49; 15",
      "StrengthUnit": "g/100g; g/100g",
      "Status": "Active",
      "LastUpdate": "2023-12-14",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20130401",
      "SamplePackage": "N",
      "IndicationAndUsage": "Protects against minor skin irritation due to diaper rash and helps seal out wetness. Helps treat and prevent diaper rash."
    },
    {
      "NDCCode": "24330-411-08",
      "PackageDescription": "71 g in 1 TUBE (24330-411-08)",
      "NDC11Code": "24330-0411-08",
      "ProductNDC": "24330-411",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro 2-in-1 Antifungal And Skin Protectant",
      "NonProprietaryName": "Miconazole Nitrate",
      "DosageFormName": "OINTMENT",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130401",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part333C",
      "LabelerName": "The Akshay Wellness Group, Inc.",
      "SubstanceName": "MICONAZOLE NITRATE",
      "StrengthNumber": "2",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2016-12-02"
    },
    {
      "NDCCode": "24330-412-02",
      "PackageDescription": "106 g in 1 TUBE (24330-412-02)",
      "NDC11Code": "24330-0412-02",
      "ProductNDC": "24330-412",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro Fragile Skin Protectant",
      "NonProprietaryName": "Petrolatum",
      "DosageFormName": "OINTMENT",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130401",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part347",
      "LabelerName": "Welmedix Llc",
      "SubstanceName": "PETROLATUM",
      "StrengthNumber": "42",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "24330-412-03",
      "PackageDescription": "142 g in 1 TUBE (24330-412-03) ",
      "NDC11Code": "24330-0412-03",
      "ProductNDC": "24330-412",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro Fragile Skin Protectant",
      "NonProprietaryName": "Petrolatum",
      "DosageFormName": "OINTMENT",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20130401",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M012",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "PETROLATUM",
      "StrengthNumber": "42",
      "StrengthUnit": "g/100g",
      "Status": "Active",
      "LastUpdate": "2023-12-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20130401",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather. helps treat and prevent diaper rash. protects chafed skin associated with diaper rash and helps protect from wetness. temporarily protects:  minor cuts  scrapes  burns."
    },
    {
      "NDCCode": "24330-413-12",
      "PackageDescription": "340 g in 1 JAR (24330-413-12) ",
      "NDC11Code": "24330-0413-12",
      "ProductNDC": "24330-413",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Welmedix Homecare Pro Fragile Skin Protectant",
      "NonProprietaryName": "Petrolatum",
      "DosageFormName": "OINTMENT",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20251115",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M016",
      "LabelerName": "Welmedix LLC",
      "SubstanceName": "PETROLATUM",
      "StrengthNumber": "42",
      "StrengthUnit": "g/100g",
      "Status": "Active",
      "LastUpdate": "2025-11-18",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20251115",
      "SamplePackage": "N",
      "IndicationAndUsage": "temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather. helps treat and prevent diaper rash. protects chafed skin associated with diaper rash and helps protect from wetness. temporarily protects:  minor cuts  scrapes  burns."
    }
  ]
}
                    
{"NDC":[{"NDCCode":"24330-111-85","ProprietaryName":"First Degree Burn","NonProprietaryName":"Benzocaine, Triclosan"},{"NDCCode":"21130-111-85","ProprietaryName":"Signature Care Pain Relief","NonProprietaryName":"Acetaminophen"},{"NDCCode":"21922-111-15","ProprietaryName":"Econazole Nitrate","NonProprietaryName":"Econazole Nitrate"},{"NDCCode":"42783-111-85","ProprietaryName":"Zithranol","NonProprietaryName":"Anthralin"},{"NDCCode":"43744-111-85","NonProprietaryName":"Bumetanide"},{"NDCCode":"58607-111-85","ProprietaryName":"Myferon 150","NonProprietaryName":"Iron Sucrose"},{"NDCCode":"69949-111-01","ProprietaryName":"Mineral Body Sunscreen Unscented","NonProprietaryName":"Zinc Oxide"},{"NDCCode":"80587-111-03","ProprietaryName":"Urea Cream 40%","NonProprietaryName":"Urea Cream 40%"},{"NDCCode":"82699-111-02","ProprietaryName":"Right Guard Sport Antiperspirant Deodorant Gel Cool","NonProprietaryName":"Right Guard Sport Antiperspirant Deodorant Gel Cool"},{"NDCCode":"17156-021-01","ProprietaryName":"Indium In 111 Oxyquinoline","NonProprietaryName":"Indium In-111 Oxyquinoline"},{"NDCCode":"54288-111-05","ProprietaryName":"Hyoscyamine Sulfate","NonProprietaryName":"Hyoscyamine Sulfate"},{"NDCCode":"59310-111-06","ProprietaryName":"Airduo Digihaler","NonProprietaryName":"Fluticasone Propionate And Salmeterol"},{"NDCCode":"69945-132-06","ProprietaryName":"Indium In 111 Chloride","NonProprietaryName":"Indium In 111 Chloride"},{"NDCCode":"72536-0920-1","ProprietaryName":"Indium In 111 Oxyquinoline","NonProprietaryName":"Indium In-111 Oxyquinoline"},{"NDCCode":"76229-123-01","ProprietaryName":"Likewise Hand Moisturizer - Sun Protectant Spf 50","NonProprietaryName":"Octinoxate, Octisalate, Zinc Oxide"},{"NDCCode":"24330-110-14","ProprietaryName":"First Degree","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-110-21","ProprietaryName":"First Degree","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-110-22","ProprietaryName":"First Degree","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-130-02","ProprietaryName":"First Degree Maximum Strength Burn","NonProprietaryName":"Pramoxine Hydrochloride"},{"NDCCode":"24330-210-01","ProprietaryName":"Sunburnt","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-210-03","ProprietaryName":"Sunburnt Advanced After-sun","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-210-06","ProprietaryName":"Sunburnt Advanced After-sun","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-210-21","ProprietaryName":"Sunburnt","NonProprietaryName":"Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria"},{"NDCCode":"24330-240-01","ProprietaryName":"Sunburnt Plus Pain Relief","NonProprietaryName":"Lidocaine Hydrochloride"},{"NDCCode":"24330-410-06","ProprietaryName":"Welmedix Homecare Pro Extra Strength Rapid Rash Relief","NonProprietaryName":"Petrolatum, Zinc Oxide"},{"NDCCode":"24330-410-07","ProprietaryName":"Welmedix Homecare Pro Extra Strength Rapid Rash Relief","NonProprietaryName":"Petrolatum, Zinc Oxide"},{"NDCCode":"24330-411-08","ProprietaryName":"Welmedix Homecare Pro 2-in-1 Antifungal And Skin Protectant","NonProprietaryName":"Miconazole Nitrate"},{"NDCCode":"24330-412-02","ProprietaryName":"Welmedix Homecare Pro Fragile Skin Protectant","NonProprietaryName":"Petrolatum"},{"NDCCode":"24330-412-03","ProprietaryName":"Welmedix Homecare Pro Fragile Skin Protectant","NonProprietaryName":"Petrolatum"},{"NDCCode":"24330-413-12","ProprietaryName":"Welmedix Homecare Pro Fragile Skin Protectant","NonProprietaryName":"Petrolatum"}]}
                    
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<NDCList>
  <NDC>
    <NDCCode>24330-111-85</NDCCode>
    <PackageDescription>89 mL in 1 CAN (24330-111-85)</PackageDescription>
    <NDC11Code>24330-0111-85</NDC11Code>
    <ProductNDC>24330-111</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>First Degree Burn</ProprietaryName>
    <NonProprietaryName>Benzocaine, Triclosan</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130201</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>The Akshay Wellness Group, Inc.</LabelerName>
    <SubstanceName>BENZOCAINE; TRICLOSAN</SubstanceName>
    <StrengthNumber>200; 1.3</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-01-01</LastUpdate>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>for temporary relief of pain and itching from minor burns, cuts and scrapes. first aid to help prevent infection in minor burns, cuts and scrapes.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>21130-111-85</NDCCode>
    <PackageDescription>1 BOTTLE in 1 CARTON (21130-111-85)  / 250 TABLET in 1 BOTTLE</PackageDescription>
    <NDC11Code>21130-0111-85</NDC11Code>
    <ProductNDC>21130-111</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Signature Care Pain Relief</ProprietaryName>
    <NonProprietaryName>Acetaminophen</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150901</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M013</ApplicationNumber>
    <LabelerName>Safeway</LabelerName>
    <SubstanceName>ACETAMINOPHEN</SubstanceName>
    <StrengthNumber>500</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-09-24</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20150901</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily relieves minor aches and pains due to:. the common cold. headache. backache. minor pain of arthritis. toothache. muscular aches. premenstrual and menstrual cramps. temporarily reduces fever.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>21922-111-15</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (21922-111-15)  / 85 g in 1 TUBE</PackageDescription>
    <NDC11Code>21922-0111-15</NDC11Code>
    <ProductNDC>21922-111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Econazole Nitrate</ProprietaryName>
    <NonProprietaryName>Econazole Nitrate</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20260701</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA076574</ApplicationNumber>
    <LabelerName>Encube Ethicals, Inc.</LabelerName>
    <SubstanceName>ECONAZOLE NITRATE</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Pharm_Classes>Azole Antifungal [EPC], Azoles [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-07-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260701</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Econazole nitrate cream is indicated for topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, Microsporum canis, Microsporum audouini, Microsporum gypseum, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis, and in the treatment of tinea versicolor.</IndicationAndUsage>
    <Description>Econazole nitrate cream contains the antifungal agent, econazole nitrate 1% in a water-miscible base consisting of pegoxol 7 stearate, peglicol 5 oleate, mineral oil, benzoic acid, butylated hydroxyanisole, and purified water. The white to off-white soft cream is for topical use only. Chemically, econazole nitrate is 1-[2-{(4-chloro-phenyl) methoxy}-2-(2, 4-dichlorophenyl) ethyl]-1H-imidazole mononitrate. Its structure is as follows.</Description>
  </NDC>
  <NDC>
    <NDCCode>42783-111-85</NDCCode>
    <PackageDescription>12 CARTON in 1 CASE (42783-111-85)  &gt; 1 TUBE in 1 CARTON &gt; 85 g in 1 TUBE</PackageDescription>
    <NDC11Code>42783-0111-85</NDC11Code>
    <ProductNDC>42783-111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Zithranol</ProprietaryName>
    <NonProprietaryName>Anthralin</NonProprietaryName>
    <DosageFormName>SHAMPOO</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20120305</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>Elorac Inc.</LabelerName>
    <SubstanceName>ANTHRALIN</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Zithranol Shampoo for the treatment of scalp psoriasis in subjects 12 years of age and older (see PRECAUTIONS). Patients should be instructed to use Zithranol Shampoo for the minimum time period necessary to achieve the desired results.</IndicationAndUsage>
    <Description>Zithranol Shampoo contains 1% anthralin in a shampoo base containing glyceryl monolaurate, glyceryl monomyristate, citric acid, sodium hydroxide, FD&amp;C Blue No. 1, Macare® G-2C, and purified water. The chemical name of anthralin is 1,8-dihydroxy-9-anthrone and its structural formula is.</Description>
  </NDC>
  <NDC>
    <NDCCode>43744-111-85</NDCCode>
    <PackageDescription>25000 g in 1 DRUM (43744-111-85)</PackageDescription>
    <NDC11Code>43744-0111-85</NDC11Code>
    <ProductNDC>43744-111</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Bumetanide</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20110707</StartMarketingDate>
    <EndMarketingDate>20130624</EndMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>CBSCHEM LIMITED</LabelerName>
    <SubstanceName>BUMETANIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20130624</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>58607-111-85</NDCCode>
    <PackageDescription>100 BLISTER PACK in 1 BOX (58607-111-85)  &gt; 10 CAPSULE in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>58607-0111-85</NDC11Code>
    <ProductNDC>58607-111</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Myferon 150</ProprietaryName>
    <NonProprietaryName>Iron Sucrose</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19961201</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>MARTIN EKWEALOR PHARMACEUTICALS, INC.</LabelerName>
    <SubstanceName>IRON SUCROSE</SubstanceName>
    <StrengthNumber>150</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Myferon 150 is indicated for the prevention and treatment of iron deficiency anemia and/or nutritional megaloblastic anemias.</IndicationAndUsage>
    <Description>Myferon 150, Polysaccharide Iron Complex capsules are a preparation of ferric Iron complexed to a low molecular weight polysaccharide. This polysaccharide is obtained by extensive hydrolysis of starch. Myferon 150 is a dark brown powder that when dissolved in water, forms a very dark brown solution. As an organic complex, polysaccharide iron contains no free iron. It is tasteless, odorless and readily soluble in water.</Description>
  </NDC>
  <NDC>
    <NDCCode>69949-111-01</NDCCode>
    <PackageDescription>85 g in 1 TUBE (69949-111-01) </PackageDescription>
    <NDC11Code>69949-0111-01</NDC11Code>
    <ProductNDC>69949-111</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Mineral Body Sunscreen Unscented</ProprietaryName>
    <NonProprietaryName>Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20230801</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M020</ApplicationNumber>
    <LabelerName>Synchronicity Spa, Inc. DBA Suntegrity</LabelerName>
    <SubstanceName>ZINC OXIDE</SubstanceName>
    <StrengthNumber>200</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-12-14</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230801</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>helps prevent sunburn. if used as directed with other sun protection measures (see Directions), decreases risk of skin cancer and early skin aging caused by the sun.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>80587-111-03</NDCCode>
    <PackageDescription>85 g in 1 BOTTLE (80587-111-03) </PackageDescription>
    <NDC11Code>80587-0111-03</NDC11Code>
    <ProductNDC>80587-111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Urea Cream 40%</ProprietaryName>
    <NonProprietaryName>Urea Cream 40%</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20211118</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>Prime Labs, LLC dba Quality CDMO</LabelerName>
    <SubstanceName>UREA</SubstanceName>
    <StrengthNumber>400</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2022-06-25</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20231231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20211118</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>82699-111-02</NDCCode>
    <PackageDescription>85 g in 1 CANISTER (82699-111-02) </PackageDescription>
    <NDC11Code>82699-0111-02</NDC11Code>
    <ProductNDC>82699-111</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Right Guard Sport Antiperspirant Deodorant Gel Cool</ProprietaryName>
    <NonProprietaryName>Right Guard Sport Antiperspirant Deodorant Gel Cool</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20241017</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M019</ApplicationNumber>
    <LabelerName>Thriving Brands LLC</LabelerName>
    <SubstanceName>ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY</SubstanceName>
    <StrengthNumber>16.4</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-01-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20241017</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>17156-021-01</NDCCode>
    <PackageDescription>1 VIAL in 1 BOX (17156-021-01)  / 1 mL in 1 VIAL</PackageDescription>
    <NDC11Code>17156-0021-01</NDC11Code>
    <ProductNDC>17156-021</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Indium In 111 Oxyquinoline</ProprietaryName>
    <NonProprietaryName>Indium In-111 Oxyquinoline</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>19851201</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA019044</ApplicationNumber>
    <LabelerName>Medi-Physics Inc. dba GE Healthcare.</LabelerName>
    <SubstanceName>INDIUM IN-111 OXYQUINOLINE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>ug/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-01-12</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>19851201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Indium In 111 Oxyquinoline Solution is indicated for radiolabeling autologous leukocytes. Indium In 111 oxyquinoline labeled leukocytes may be used as an adjunct in the detection of inflammatory processes to which leukocytes migrate, such as those associated with abscesses or other infection, following reinjection and detection by appropriate imaging procedures. The degree of accuracy may vary with labeling techniques and with the size, location and nature of the inflammatory process. Indium In 111 oxyquinoline labeled leukocyte imaging is not the preferred technique for the initial evaluation of patients with a high clinical probability of an abscess in a known location. Ultrasound or computed tomography may provide a better anatomical delineation of the infectious process and information may be obtained more quickly than with labeled leukocytes. If localization by these techniques is successful, labeled leukocytes should not be used as a confirmatory procedure. If localization or diagnosis by these methods fails or is ambiguous, indium In 111 oxyquinoline labeled leukocyte imaging may be appropriate.</IndicationAndUsage>
    <Description>Indium In 111 Oxyquinoline (oxine) Solution is a diagnostic radiopharmaceutical intended for radiolabeling autologous leukocytes. It is supplied as a sterile, non-pyrogenic, isotonic aqueous solution with a pH range of 6.5 to 7.5 [sodium hydroxide and hydrochloric acid may be used to adjust the pH]. Each mL of the solution contains 37 MBq, 1 mCi of indium In 111 [no carrier added, &gt;1.85 GBq/mcg indium (&gt;50 mCi/mcg indium)] at calibration time, 50 mcg oxyquinoline, 100 mcg polysorbate 80, and 6 mg of HEPES (N-2-hydroxyethyl-piperazine-N'-2-ethane sulfonic acid) buffer in 0.75% Sodium Chloride Solution. The drug is intended to be used as a single-dose vial and contains no bacteriostatic agent. The radionuclidic impurity limit for indium 114m is not greater than 37 kBq, 1 µCi of indium 114m per 37 MBq, 1 mCi of indium In 111 at the time of calibration. The radionuclidic composition at expiration time is not less than 99.75% of indium In 111 and not more than 0.25% of indium In 114m/114. Chemical name: Indium In 111 Oxyquinoline. The precise structure of the indium In 111 oxyquinoline complex is unknown at this time. The empirical formula is (C9H6NO)3 In 111.</Description>
  </NDC>
  <NDC>
    <NDCCode>54288-111-05</NDCCode>
    <PackageDescription>5 VIAL in 1 CARTON (54288-111-05)  / 1 mL in 1 VIAL (54288-111-01) </PackageDescription>
    <NDC11Code>54288-0111-05</NDC11Code>
    <ProductNDC>54288-111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Hyoscyamine Sulfate</ProprietaryName>
    <NonProprietaryName>Hyoscyamine Sulfate</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20191018</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>BPI Labs LLC</LabelerName>
    <SubstanceName>HYOSCYAMINE SULFATE</SubstanceName>
    <StrengthNumber>.5</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-12-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20191018</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Hyoscyamine sulfate Injection, USP is effective as adjunctive therapy in the treatment of peptic ulcer. In acute episodes, Hyoscyamine sulfate Injection, USP can be used to control gastric secretion, visceral spasm and hypermotility in spastic colitis, spastic bladder, cystitis, pylorospasm, and associated abdominal cramps. For use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and functional gastrointestinal disorders. Also as adjunctive therapy in the treatment of neurogenic bladder and neurogenic bowel disturbances (including the splenic flexure syndrome and neurogenic colon). Parenterally administered Hyoscyamine sulfate Injection, USP is also effective in reducing gastrointestinal motility to facilitate diagnostic procedures such as endoscopy or hypotonic duodenography. Hyoscyamine sulfate Injection, USP may be used to reduce pain and hypersecretion in pancreatitis, in certain cases of partial heart block associated with vagal activity, and as an antidote for poisoning by anticholinesterase agents. In Anesthesia. Hyoscyamine sulfate Injection, USP is indicated as a pre-operative antimuscarinic to reduce salivary, tracheobronchial, and pharyngeal secretions, to reduce the volume and acidity of gastric secretions, and to block cardiac vagal inhibitory reflexes during induction of anesthesia and intubation. Hyoscyamine sulfate Injection, USP protects against the peripheral muscarinic effects such as bradycardia and excessive secretions produced by halogenated hydrocarbons and cholinergic agents such as physostigmine, neostigmine, and pyridostigmine given to reverse the actions of curariform agents. In Urology. Hyoscyamine sulfate Injection, USP may also be used intravenously to improve radiologic visibility of the kidneys. It is also indicated along with morphine or other narcotics in symptomatic relief of biliary and renal colic.</IndicationAndUsage>
    <Description>Hyoscyamine sulfate injection, USP is a sterile solution containing 0.5 mg hyoscyamine sulfate per mL in water for injection. Hyoscyamine sulfate Injection, USP is one of the principal anticholinergic/antispasmodic components of belladonna alkaloids. The empirical formula is (C 17H 23NO 3) 2H 2SO 42H 20 and the molecular weight is 712.85. Chemically, it is benzeneacetic acid, α-(hydroxymethyl)-,8-methyl-8-azabicyclo [3.2.1.] oct-3-yl ester, [3(S)-endo]-, sulfate (2:1), dihydrate with the following structure. The 1 mL vials contain as inactive ingredients: water for injection, pH is adjusted with hydrochloric acid when necessary.</Description>
  </NDC>
  <NDC>
    <NDCCode>59310-111-06</NDCCode>
    <PackageDescription>1 POUCH in 1 CARTON (59310-111-06)  / 1 INHALER in 1 POUCH / 1 POWDER, METERED in 1 INHALER</PackageDescription>
    <NDC11Code>59310-0111-06</NDC11Code>
    <ProductNDC>59310-111</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Airduo Digihaler</ProprietaryName>
    <NonProprietaryName>Fluticasone Propionate And Salmeterol</NonProprietaryName>
    <DosageFormName>POWDER, METERED</DosageFormName>
    <RouteName>RESPIRATORY (INHALATION)</RouteName>
    <StartMarketingDate>20200915</StartMarketingDate>
    <EndMarketingDate>20240831</EndMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA208799</ApplicationNumber>
    <LabelerName>Teva Respiratory, LLC</LabelerName>
    <SubstanceName>FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE</SubstanceName>
    <StrengthNumber>55; 14</StrengthNumber>
    <StrengthUnit>ug/1; ug/1</StrengthUnit>
    <Pharm_Classes>Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2024-09-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20200915</StartMarketingDatePackage>
    <EndMarketingDatePackage>20240831</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>AirDuo® Digihaler® is indicated for the treatment of asthma in adult and pediatric patients aged 12 years and older. AirDuo Digihaler should be used for patients not adequately controlled on a long term asthma control medication such as an inhaled corticosteroid or whose disease warrants initiation of treatment with both an inhaled corticosteroid and long acting beta2-adrenergic agonist (LABA). Limitations of Use:. AirDuo Digihaler is not indicated for the relief of acute bronchospasm.</IndicationAndUsage>
    <Description>AirDuo Digihaler 55/14 mcg, AirDuo Digihaler 113/14 mcg and AirDuo Digihaler 232/14 mcg are combinations of fluticasone propionate and salmeterol. Fluticasone Propionate. One active component of AirDuo Digihaler is fluticasone propionate, a corticosteroid having the chemical name S-(fluoromethyl) 6α,9-difluoro-11ß,17-dihydroxy-16α-methyl-3-oxoandrosta-1,4-diene-17ß-carbothioate, 17-propionate, and the following chemical structure. Fluticasone propionate is a white powder with a molecular weight of 500.6, and the empirical formula is C25H31F3O5S. It is practically insoluble in water, freely soluble in dimethyl sulfoxide and dimethylformamide, and slightly soluble in methanol and 95% ethanol. Salmeterol Xinafoate. The other active component of AirDuo Digihaler is salmeterol xinafoate, a beta2–adrenergic bronchodilator. Salmeterol xinafoate is the racemic form of the 1‑hydroxy‑2‑naphthoic acid salt of salmeterol. It has the chemical name 4-hydroxy-α -[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-1,3-benzenedimethanol, 1-hydroxy-2-naphthalenecarboxylate and the following chemical structure. Salmeterol xinafoate is a white powder with a molecular weight of 603.8, and the empirical formula is C25H37NO4C11H8O3. It is freely soluble in methanol; slightly soluble in ethanol, chloroform, and isopropanol; and sparingly soluble in water. AirDuo Digihaler. AirDuo Digihaler is a multidose dry powder inhaler (MDPI) with an electronic module, for oral inhalation only. It contains fluticasone propionate, salmeterol xinafoate, and lactose monohydrate (which may contain milk proteins). The opening of the mouthpiece cover meters 5.5 mg of the formulation from the device reservoir, which contains 55 mcg, 113 mcg, or 232 mcg of fluticasone propionate, and 14 mcg of salmeterol base (equivalent to 20.3 mcg of salmeterol xinafoate). Patient inhalation through the mouthpiece causes the deagglomeration and aerosolization of the drug particles as the formulation moves through the cyclone component of the device. This is followed by dispersion into the airstream. Under standardized in vitro test conditions, the AirDuo Digihaler inhaler delivers 49 mcg, 100 mcg, or 202 mcg of fluticasone propionate and 12.75 mcg of salmeterol base (equivalent to 18.5 mcg of salmeterol xinafoate), with lactose from the mouthpiece when tested at a flow rate of 85 L/min for 1.4 seconds. The amount of drug delivered to the lung will depend on patient factors such as inspiratory flow profiles. In adult subjects (N=50, aged 18 to 45 years) with asthma, mean peak inspiratory flow (PIF) through the MDPI was 108.28 L/min (range: 70.37 to 129.24 L/min). In adolescent subjects (N=50, aged 12 to 17 years) with asthma, mean peak inspiratory flow (PIF) through the MDPI was 106.72 L/min (range: 73.64 to 125.51 L/min). AirDuo Digihaler includes a QR code (on the top of the inhaler), and contains a built-in electronic module which automatically detects, records and stores data on inhaler events, including peak inspiratory flow rate (L/min). AirDuo Digihaler may pair with and transmit data to the mobile App where inhaler events are categorized.</Description>
  </NDC>
  <NDC>
    <NDCCode>69945-132-06</NDCCode>
    <PackageDescription>1 VIAL, GLASS in 1 CAN (69945-132-06)  &gt; .5 mL in 1 VIAL, GLASS</PackageDescription>
    <NDC11Code>69945-0132-06</NDC11Code>
    <ProductNDC>69945-132</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Indium In 111 Chloride</ProprietaryName>
    <NonProprietaryName>Indium In 111 Chloride</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20071207</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA019841</ApplicationNumber>
    <LabelerName>Curium US LLC</LabelerName>
    <SubstanceName>INDIUM CHLORIDE IN-111</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mCi/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2024-09-24</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20071207</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Indium In 111 Chloride Sterile Solution is indicated for radiolabeling ProstaScint preparations used for in vivo diagnostic imaging procedures. It is also indicated for radiolabeling Zevalin preparations used for Radioimmunotherapy procedures. Please refer to the package insert for ProstaScint or Zevalin for information on the final drug product.</IndicationAndUsage>
    <Description>Indium In 111 Chloride Sterile Solution is indicated for radiolabeling ProstaScint preparations used for in vivo diagnostic imaging procedures. It is also indicated for radiolabeling Zevalin preparations used for Radioimmunotherapy procedures. It is supplied as a sterile, non-pyrogenic solution of Indium In 111 Chloride in 0.05 molar hydrochloric acid. No carrier has been added to the solution. Each 0.5 milliliter of the solution contains 185 megabequerels (5 millicuries) of Indium In 111 Chloride at time of calibration (specific activity of &gt;1.85 GBq/μg Indium; &gt;50 mCi/μg Indium at this time of calibration). The solution pH is 1.1 to 1.4.</Description>
  </NDC>
  <NDC>
    <NDCCode>72536-0920-1</NDCCode>
    <PackageDescription>1 mL in 1 VIAL, SINGLE-DOSE (72536-0920-1) </PackageDescription>
    <NDC11Code>72536-0920-01</NDC11Code>
    <ProductNDC>72536-0920</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Indium In 111 Oxyquinoline</ProprietaryName>
    <NonProprietaryName>Indium In-111 Oxyquinoline</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20190927</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA202586</ApplicationNumber>
    <LabelerName>BWXT Medical Ltd.</LabelerName>
    <SubstanceName>INDIUM IN-111 OXYQUINOLINE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mCi/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-11-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190927</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Indium In 111 oxyquinoline is indicated for radiolabeling autologous leukocytes. Indium In 111 oxyquinoline labeled leukocytes may be used as an adjunct in the detection of inflammatory processes to which leukocytes migrate, such as those associated with abscesses or other infection, following reinjection and detection by appropriate imaging procedures. The degree of accuracy may vary with labeling techniques and with the size, location and nature of the inflammatory process. Indium In 111 oxyquinoline labeled leukocyte imaging is not the preferred technique for the initial evaluation of patients with a high clinical probability of an abscess in a known location. Ultrasound or computed tomography may provide a better anatomical delineation of the infectious process and information may be obtained more quickly than with labeled leukocytes. If localization by these techniques is successful, labeled leukocytes should not be used as a confirmatory procedure. If localization or diagnosis by these methods fails or is ambiguous, indium In 111 oxyquinoline labeled leukocyte imaging may be appropriate.</IndicationAndUsage>
    <Description>Indium In 111 oxyquinoline (oxine) is a diagnostic radiopharmaceutical intended for radiolabeling autologous leukocytes. It is supplied as a sterile, non-pyrogenic, isotonic aqueous solution with a pH range of 6.5 to 7.5. Each mL of the solution contains 37 MBq, 1 mCi of indium In 111 [no carrier added, &gt;1.85 GBq/µg indium (&gt;50 mCi/µg indium)] at calibration time, 50 µg oxyquinoline, 100 µg polysorbate 80, and 6 mg of HEPES (N-2-hydroxyethyl-piperazine-N’-2-ethane sulfonic acid) buffer in 0.75% sodium chloride solution. The drug is intended for single use only and contains no bacteriostatic agent. The radionuclidic impurity limit for indium 114m is not greater than 37 kBq, 1 µCi of indium 114m per 37 MBq, 1 mCi of indium In 111 at the time of calibration. The radionuclidic composition at expiration time is not less than 99.75% of indium In 111 and not more than 0.25% of indium In 114m/114. Chemical name: Indium In 111 Oxyquinoline. The precise structure of the indium In 111 oxyquinoline complex is unknown at this time. The empirical formula is (C9H6NO)3 In 111.</Description>
  </NDC>
  <NDC>
    <NDCCode>76229-123-01</NDCCode>
    <PackageDescription>1 BOTTLE in 1 PACKAGE (76229-123-01)  / 85 mL in 1 BOTTLE</PackageDescription>
    <NDC11Code>76229-0123-01</NDC11Code>
    <ProductNDC>76229-123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Likewise Hand Moisturizer - Sun Protectant Spf 50</ProprietaryName>
    <NonProprietaryName>Octinoxate, Octisalate, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20110620</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M020</ApplicationNumber>
    <LabelerName>Likewise Incorporated</LabelerName>
    <SubstanceName>OCTINOXATE; OCTISALATE; ZINC OXIDE</SubstanceName>
    <StrengthNumber>75; 50; 111.6</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL; mg/mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-12-18</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171219</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Helps prevent sunburn. Higher SPF provides more protection. Retains SPF after 40 minutes of activity in water or vigorous sweating.</IndicationAndUsage>
    <Description>protect hydrate renew  . . . . . . .   NORMAL TO DRY SKIN  Daily moisturizer + Sunscreen  Dermatologist developed  Calms and softens dry, irritated skin with Niacinamide  Anti-aging antioxidants reverse daily damage and rejuvenate skin  Contains Vitamins B, C and E and Natural Soy to improve skin tone and texture  Works wonders as a nighttime moisturizer, too Non-greasy light coverage (apply 1 pea-size drop)  Delightfully fragrance free  . . . . . . .  LikewiseSkinCare.com  LIKEWISE INCORPORATED  200 COOL SPRINGS BOULEVARD  FRANKLIN, TENNESSEE 37067  IN CASE OF ADVERSE REACTION: 877.778.9546.</Description>
  </NDC>
  <NDC>
    <NDCCode>24330-110-14</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-110-14)  &gt; 14 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0110-14</NDC11Code>
    <ProductNDC>24330-110</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>First Degree</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>TINCTURE</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2015-08-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20140501</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-110-21</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-110-21)  &gt; 21 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0110-21</NDC11Code>
    <ProductNDC>24330-110</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>First Degree</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>TINCTURE</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2015-08-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20070101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-110-22</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-110-22)  &gt; 21 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0110-22</NDC11Code>
    <ProductNDC>24330-110</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>First Degree</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>TINCTURE</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2015-08-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20150301</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves symptoms such as minor skin pain, rawness and itching due to: 1 minor burns, 2 insect bites, 3 minor scrapes, 4 scalds.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-130-02</NDCCode>
    <PackageDescription>1 TUBE in 1 BOX (24330-130-02)  &gt; 21 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0130-02</NDC11Code>
    <ProductNDC>24330-130</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>First Degree Maximum Strength Burn</ProprietaryName>
    <NonProprietaryName>Pramoxine Hydrochloride</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20170309</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>PRAMOXINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2017-04-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20170309</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of pain and itching associated with: 1 minor burns, 2 insect bites, 3 sunburns, 4 minor cuts, 5 scrapes, 6 minor skin irritations.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-210-01</NDCCode>
    <PackageDescription>1 TUBE in 1 POUCH (24330-210-01)  &gt; 7.1 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0210-01</NDC11Code>
    <ProductNDC>24330-210</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunburnt</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>TINCTURE</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2018-04-09</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>24330-210-03</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-210-03)  &gt; 71 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0210-03</NDC11Code>
    <ProductNDC>24330-210</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunburnt Advanced After-sun</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2018-04-09</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20160901</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves symptoms of mild and moderate sunburn such as: 1 overheated skin, 2 redness, 3 rawness, 4 itching, 5 dryness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-210-06</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-210-06)  &gt; 170 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0210-06</NDC11Code>
    <ProductNDC>24330-210</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunburnt Advanced After-sun</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2018-04-09</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20160901</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves symptoms of mild and moderate sunburn such as: 1 overheated skin, 2 redness, 3 rawness, 4 itching, 5 dryness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-210-21</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-210-21)  &gt; 21.3 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0210-21</NDC11Code>
    <ProductNDC>24330-210</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunburnt</ProprietaryName>
    <NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName>
    <DosageFormName>TINCTURE</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20070101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA</SubstanceName>
    <StrengthNumber>1; 1; 3</StrengthNumber>
    <StrengthUnit>[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2018-04-09</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>24330-240-01</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (24330-240-01)  &gt; 142 g in 1 TUBE</PackageDescription>
    <NDC11Code>24330-0240-01</NDC11Code>
    <ProductNDC>24330-240</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Sunburnt Plus Pain Relief</ProprietaryName>
    <NonProprietaryName>Lidocaine Hydrochloride</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20180315</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>Welmedix LLC dba Welmedix Consumer Healthcare</LabelerName>
    <SubstanceName>LIDOCAINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Pharm_Classes>Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2018-03-15</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180315</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Temporarily relieves pain and itching due to: 1 sunburn, 2 minor burns, 3 insect bites, 4 minor skin irritations, 5 minor cuts, 6 scrapes.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-410-06</NDCCode>
    <PackageDescription>57 g in 1 TUBE (24330-410-06)</PackageDescription>
    <NDC11Code>24330-0410-06</NDC11Code>
    <ProductNDC>24330-410</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro Extra Strength Rapid Rash Relief</ProprietaryName>
    <NonProprietaryName>Petrolatum, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130401</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>Welmedix Llc</LabelerName>
    <SubstanceName>PETROLATUM; ZINC OXIDE</SubstanceName>
    <StrengthNumber>49; 15</StrengthNumber>
    <StrengthUnit>g/100g; g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>24330-410-07</NDCCode>
    <PackageDescription>113 g in 1 TUBE (24330-410-07) </PackageDescription>
    <NDC11Code>24330-0410-07</NDC11Code>
    <ProductNDC>24330-410</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro Extra Strength Rapid Rash Relief</ProprietaryName>
    <NonProprietaryName>Petrolatum, Zinc Oxide</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130401</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M012</ApplicationNumber>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>PETROLATUM; ZINC OXIDE</SubstanceName>
    <StrengthNumber>49; 15</StrengthNumber>
    <StrengthUnit>g/100g; g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-12-14</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20130401</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Protects against minor skin irritation due to diaper rash and helps seal out wetness. Helps treat and prevent diaper rash.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-411-08</NDCCode>
    <PackageDescription>71 g in 1 TUBE (24330-411-08)</PackageDescription>
    <NDC11Code>24330-0411-08</NDC11Code>
    <ProductNDC>24330-411</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro 2-in-1 Antifungal And Skin Protectant</ProprietaryName>
    <NonProprietaryName>Miconazole Nitrate</NonProprietaryName>
    <DosageFormName>OINTMENT</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130401</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part333C</ApplicationNumber>
    <LabelerName>The Akshay Wellness Group, Inc.</LabelerName>
    <SubstanceName>MICONAZOLE NITRATE</SubstanceName>
    <StrengthNumber>2</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2016-12-02</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>24330-412-02</NDCCode>
    <PackageDescription>106 g in 1 TUBE (24330-412-02)</PackageDescription>
    <NDC11Code>24330-0412-02</NDC11Code>
    <ProductNDC>24330-412</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName>
    <NonProprietaryName>Petrolatum</NonProprietaryName>
    <DosageFormName>OINTMENT</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130401</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part347</ApplicationNumber>
    <LabelerName>Welmedix Llc</LabelerName>
    <SubstanceName>PETROLATUM</SubstanceName>
    <StrengthNumber>42</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>24330-412-03</NDCCode>
    <PackageDescription>142 g in 1 TUBE (24330-412-03) </PackageDescription>
    <NDC11Code>24330-0412-03</NDC11Code>
    <ProductNDC>24330-412</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName>
    <NonProprietaryName>Petrolatum</NonProprietaryName>
    <DosageFormName>OINTMENT</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20130401</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M012</ApplicationNumber>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>PETROLATUM</SubstanceName>
    <StrengthNumber>42</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-12-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20130401</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather. helps treat and prevent diaper rash. protects chafed skin associated with diaper rash and helps protect from wetness. temporarily protects:  minor cuts  scrapes  burns.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>24330-413-12</NDCCode>
    <PackageDescription>340 g in 1 JAR (24330-413-12) </PackageDescription>
    <NDC11Code>24330-0413-12</NDC11Code>
    <ProductNDC>24330-413</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName>
    <NonProprietaryName>Petrolatum</NonProprietaryName>
    <DosageFormName>OINTMENT</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20251115</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M016</ApplicationNumber>
    <LabelerName>Welmedix LLC</LabelerName>
    <SubstanceName>PETROLATUM</SubstanceName>
    <StrengthNumber>42</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-11-18</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20251115</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>temporarily protects and helps relieve chapped or cracked skin. helps protect from the drying effects of wind and cold weather. helps treat and prevent diaper rash. protects chafed skin associated with diaper rash and helps protect from wetness. temporarily protects:  minor cuts  scrapes  burns.</IndicationAndUsage>
  </NDC>
</NDCList>
                    
<NDCList><NDC><NDCCode>24330-111-85</NDCCode><ProprietaryName>First Degree Burn</ProprietaryName><NonProprietaryName>Benzocaine, Triclosan</NonProprietaryName></NDC><NDC><NDCCode>21130-111-85</NDCCode><ProprietaryName>Signature Care Pain Relief</ProprietaryName><NonProprietaryName>Acetaminophen</NonProprietaryName></NDC><NDC><NDCCode>21922-111-15</NDCCode><ProprietaryName>Econazole Nitrate</ProprietaryName><NonProprietaryName>Econazole Nitrate</NonProprietaryName></NDC><NDC><NDCCode>42783-111-85</NDCCode><ProprietaryName>Zithranol</ProprietaryName><NonProprietaryName>Anthralin</NonProprietaryName></NDC><NDC><NDCCode>43744-111-85</NDCCode><NonProprietaryName>Bumetanide</NonProprietaryName></NDC><NDC><NDCCode>58607-111-85</NDCCode><ProprietaryName>Myferon 150</ProprietaryName><NonProprietaryName>Iron Sucrose</NonProprietaryName></NDC><NDC><NDCCode>69949-111-01</NDCCode><ProprietaryName>Mineral Body Sunscreen Unscented</ProprietaryName><NonProprietaryName>Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>80587-111-03</NDCCode><ProprietaryName>Urea Cream 40%</ProprietaryName><NonProprietaryName>Urea Cream 40%</NonProprietaryName></NDC><NDC><NDCCode>82699-111-02</NDCCode><ProprietaryName>Right Guard Sport Antiperspirant Deodorant Gel Cool</ProprietaryName><NonProprietaryName>Right Guard Sport Antiperspirant Deodorant Gel Cool</NonProprietaryName></NDC><NDC><NDCCode>17156-021-01</NDCCode><ProprietaryName>Indium In 111 Oxyquinoline</ProprietaryName><NonProprietaryName>Indium In-111 Oxyquinoline</NonProprietaryName></NDC><NDC><NDCCode>54288-111-05</NDCCode><ProprietaryName>Hyoscyamine Sulfate</ProprietaryName><NonProprietaryName>Hyoscyamine Sulfate</NonProprietaryName></NDC><NDC><NDCCode>59310-111-06</NDCCode><ProprietaryName>Airduo Digihaler</ProprietaryName><NonProprietaryName>Fluticasone Propionate And Salmeterol</NonProprietaryName></NDC><NDC><NDCCode>69945-132-06</NDCCode><ProprietaryName>Indium In 111 Chloride</ProprietaryName><NonProprietaryName>Indium In 111 Chloride</NonProprietaryName></NDC><NDC><NDCCode>72536-0920-1</NDCCode><ProprietaryName>Indium In 111 Oxyquinoline</ProprietaryName><NonProprietaryName>Indium In-111 Oxyquinoline</NonProprietaryName></NDC><NDC><NDCCode>76229-123-01</NDCCode><ProprietaryName>Likewise Hand Moisturizer - Sun Protectant Spf 50</ProprietaryName><NonProprietaryName>Octinoxate, Octisalate, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>24330-110-14</NDCCode><ProprietaryName>First Degree</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-110-21</NDCCode><ProprietaryName>First Degree</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-110-22</NDCCode><ProprietaryName>First Degree</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-130-02</NDCCode><ProprietaryName>First Degree Maximum Strength Burn</ProprietaryName><NonProprietaryName>Pramoxine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>24330-210-01</NDCCode><ProprietaryName>Sunburnt</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-210-03</NDCCode><ProprietaryName>Sunburnt Advanced After-sun</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-210-06</NDCCode><ProprietaryName>Sunburnt Advanced After-sun</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-210-21</NDCCode><ProprietaryName>Sunburnt</ProprietaryName><NonProprietaryName>Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria</NonProprietaryName></NDC><NDC><NDCCode>24330-240-01</NDCCode><ProprietaryName>Sunburnt Plus Pain Relief</ProprietaryName><NonProprietaryName>Lidocaine Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>24330-410-06</NDCCode><ProprietaryName>Welmedix Homecare Pro Extra Strength Rapid Rash Relief</ProprietaryName><NonProprietaryName>Petrolatum, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>24330-410-07</NDCCode><ProprietaryName>Welmedix Homecare Pro Extra Strength Rapid Rash Relief</ProprietaryName><NonProprietaryName>Petrolatum, Zinc Oxide</NonProprietaryName></NDC><NDC><NDCCode>24330-411-08</NDCCode><ProprietaryName>Welmedix Homecare Pro 2-in-1 Antifungal And Skin Protectant</ProprietaryName><NonProprietaryName>Miconazole Nitrate</NonProprietaryName></NDC><NDC><NDCCode>24330-412-02</NDCCode><ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName><NonProprietaryName>Petrolatum</NonProprietaryName></NDC><NDC><NDCCode>24330-412-03</NDCCode><ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName><NonProprietaryName>Petrolatum</NonProprietaryName></NDC><NDC><NDCCode>24330-413-12</NDCCode><ProprietaryName>Welmedix Homecare Pro Fragile Skin Protectant</ProprietaryName><NonProprietaryName>Petrolatum</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",
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      "PracticeLocationAddressCityName": "WOODSTOCK",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06281-2225",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "860-821-3406",
      "PracticeLocationAddressFaxNumber": "860-821-3407",
      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

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",
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}
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