RESTful Lookup — Test-Drive (2007 – 2026)

Query complete (32 ms elapsed)

{
  "NDC": [
    {
      "NDCCode": "62795-1123-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1123-2) ",
      "NDC11Code": "62795-1123-02",
      "ProductNDC": "62795-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Hendel Nerve Pain Relief",
      "NonProprietaryName": "Daphne Mezereum Bark, Arnica Montana, Arsenic Trioxide, Atropa Belladonna, Citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, Hypericum Perforatum, Ruta Graveolens Flowering Top, And Toxicodendron Pubescens Leaf",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20160801",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "DAPHNE MEZEREUM BARK; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM; HYPERICUM PERFORATUM; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF",
      "StrengthNumber": "3; 6; 6; 6; 6; 6; 6; 6; 12",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-01-30",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20160801",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "0008-1123-12",
      "PackageDescription": "1 POUCH in 1 CARTON (0008-1123-12)  / 2 BLISTER PACK in 1 POUCH / 15 TABLET, FILM COATED in 1 BLISTER PACK",
      "NDC11Code": "00008-1123-12",
      "ProductNDC": "0008-1123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Duavee",
      "NonProprietaryName": "Conjugated Estrogens/bazedoxifene",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20131003",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA022247",
      "LabelerName": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.",
      "SubstanceName": "ESTROGENS, CONJUGATED; BAZEDOXIFENE ACETATE",
      "StrengthNumber": ".45; 20",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Estrogen Agonist/Antagonist [EPC], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS], Selective Estrogen Receptor Modulators [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-04-29",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20131003",
      "SamplePackage": "N",
      "IndicationAndUsage": "DUAVEE is indicated in women with a uterus for.",
      "Description": "DUAVEE (conjugated estrogens/bazedoxifene), contains conjugated estrogens with bazedoxifene, an estrogen agonist/antagonist. Conjugated estrogens are purified from pregnant mares' urine and consist of the sodium salts of water-soluble estrogen sulfates blended to represent the average composition of material derived from pregnant mares' urine. Conjugated estrogens are a mixture of sodium estrone sulfate and sodium equilin sulfate, and also contain as concomitant components, sodium sulfate conjugates, 17α-dihydroequilin, 17α-estradiol, and 17β-dihydroequilin. Bazedoxifene is supplied as the acetate salt (bazedoxifene acetate) and has the chemical name 1H-Indol-5-ol, 1-[[4-[2-(hexahydro-1H-azepin-1-yl) ethoxy]phenyl]methyl]-2-(4-hydroxyphenyl)-3-methyl-, monoacetate. The empirical formula is C30H34N2O3 ∙ C2H4O2, and the molecular weight is 530.65. Bazedoxifene acetate is a white to tan powder. The aqueous solubility of bazedoxifene is pH-dependent. Solubility is higher at lower pH. The solubility of bazedoxifene acetate in unbuffered sterile water was measured to be 923 microgramsA/mL at pH 5.4. The following represents the chemical structure of bazedoxifene acetate:. DUAVEE is available for oral administration as tablets containing 0.45 mg of conjugated estrogens with 20 mg of bazedoxifene (equivalent to 22.6 mg of bazedoxifene acetate). Each tablet of DUAVEE contains the following inactive ingredients: calcium phosphate tribasic, hydroxypropyl cellulose, microcrystalline cellulose, powdered cellulose, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, sucrose, ascorbic acid, sucrose palmitic acid ester, hydroxyethylcellulose, titanium dioxide, red iron oxide, yellow iron oxide, black iron oxide, povidone, polydextrose, maltitol, poloxamer 188, propylene glycol, and isopropyl alcohol."
    },
    {
      "NDCCode": "17856-1123-2",
      "PackageDescription": "48 SYRINGE in 1 BOX, UNIT-DOSE (17856-1123-2)  / 5 mL in 1 SYRINGE (17856-1123-6) ",
      "NDC11Code": "17856-1123-02",
      "ProductNDC": "17856-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Max Relief Junior Grape",
      "NonProprietaryName": "Childrens Acetaminophen",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240701",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M013",
      "LabelerName": "ATLANTIC BIOLOGICALS CORP.",
      "SubstanceName": "ACETAMINOPHEN",
      "StrengthNumber": "160",
      "StrengthUnit": "mg/5mL",
      "Status": "Active",
      "LastUpdate": "2026-05-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20250210",
      "SamplePackage": "N",
      "IndicationAndUsage": "taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning)."
    },
    {
      "NDCCode": "17856-1123-4",
      "PackageDescription": "120 SYRINGE in 1 BOX, UNIT-DOSE (17856-1123-4)  / 2.5 mL in 1 SYRINGE (17856-1123-8) ",
      "NDC11Code": "17856-1123-04",
      "ProductNDC": "17856-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Max Relief Junior Grape",
      "NonProprietaryName": "Childrens Acetaminophen",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240701",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M013",
      "LabelerName": "ATLANTIC BIOLOGICALS CORP.",
      "SubstanceName": "ACETAMINOPHEN",
      "StrengthNumber": "160",
      "StrengthUnit": "mg/5mL",
      "Status": "Active",
      "LastUpdate": "2026-05-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20250210",
      "SamplePackage": "N",
      "IndicationAndUsage": "taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning)."
    },
    {
      "NDCCode": "36987-1123-2",
      "PackageDescription": "10 mL in 1 VIAL, MULTI-DOSE (36987-1123-2)",
      "NDC11Code": "36987-1123-02",
      "ProductNDC": "36987-1123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "House Dust",
      "NonProprietaryName": "House Dust",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRADERMAL; SUBCUTANEOUS",
      "StartMarketingDate": "19720829",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA102192",
      "LabelerName": "Nelco Laboratories, Inc.",
      "SubstanceName": "HOUSE DUST",
      "StrengthNumber": "10000",
      "StrengthUnit": "[PNU]/mL",
      "Pharm_Classes": "Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],House Dust [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.",
      "Description": "Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts). For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections."
    },
    {
      "NDCCode": "37662-1123-2",
      "PackageDescription": "1200 PELLET in 1 BOTTLE, GLASS (37662-1123-2) ",
      "NDC11Code": "37662-1123-02",
      "ProductNDC": "37662-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Manganum Metallicum",
      "NonProprietaryName": "Manganum Metallicum",
      "DosageFormName": "PELLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20220801",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Hahnemann Laboratories, INC.",
      "SubstanceName": "MANGANESE",
      "StrengthNumber": "6",
      "StrengthUnit": "[hp_C]/1",
      "Status": "Active",
      "LastUpdate": "2022-08-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220801",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "48951-1123-2",
      "PackageDescription": "1350 PELLET in 1 BOTTLE, GLASS (48951-1123-2) ",
      "NDC11Code": "48951-1123-02",
      "ProductNDC": "48951-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Arnica E Pl. Tota 2",
      "NonProprietaryName": "Arnica E Pl. Tota 2",
      "DosageFormName": "PELLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20090901",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Uriel Pharmacy Inc.",
      "SubstanceName": "ARNICA MONTANA",
      "StrengthNumber": "2",
      "StrengthUnit": "[hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2020-11-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20090901",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "62699-1123-2",
      "PackageDescription": "12 BOX in 1 BOX (62699-1123-2)  > 1 TUBE in 1 BOX > 50 g in 1 TUBE",
      "NDC11Code": "62699-1123-02",
      "ProductNDC": "62699-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Golden Sunshine Herbal",
      "NonProprietaryName": "Topical Analgesic",
      "DosageFormName": "CREAM",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20100615",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part348",
      "LabelerName": "Nan Mei Pharmaceutical Co., Ltd.",
      "SubstanceName": "MENTHOL; METHYL SALICYLATE",
      "StrengthNumber": ".02; .005",
      "StrengthUnit": "g/g; g/g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "62991-1123-2",
      "PackageDescription": "100 g in 1 JAR (62991-1123-2) ",
      "NDC11Code": "62991-1123-02",
      "ProductNDC": "62991-1123",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Progesterone Wettable",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20090623",
      "MarketingCategoryName": "BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING",
      "LabelerName": "LETCO MEDICAL, LLC",
      "SubstanceName": "PROGESTERONE",
      "StrengthNumber": "1",
      "StrengthUnit": "g/g",
      "Status": "Unfinished",
      "LastUpdate": "2026-04-09",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "23-JUN-09"
    },
    {
      "NDCCode": "64942-1123-2",
      "PackageDescription": "12 g in 1 CONTAINER (64942-1123-2)",
      "NDC11Code": "64942-1123-02",
      "ProductNDC": "64942-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Dove Men Plus Care",
      "ProprietaryNameSuffix": "Clean Comfort Antiperspirant And Deodorant",
      "NonProprietaryName": "Aluminum Zirconium Tetrachlorohydrex Gly",
      "DosageFormName": "STICK",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20101006",
      "MarketingCategoryName": "OTC MONOGRAPH FINAL",
      "ApplicationNumber": "part350",
      "LabelerName": "Conopco Inc. d/b/a Unilever",
      "SubstanceName": "ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY",
      "StrengthNumber": "14.8",
      "StrengthUnit": "g/100g",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "70771-1123-8",
      "PackageDescription": "3 BLISTER PACK in 1 CARTON (70771-1123-8)  > 10 TABLET in 1 BLISTER PACK (70771-1123-2) ",
      "NDC11Code": "70771-1123-08",
      "ProductNDC": "70771-1123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Telmisartan And Hydrochlorothiazide",
      "NonProprietaryName": "Telmisartan And Hydrochlorothiazide",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20171012",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA204221",
      "LabelerName": "Zydus Lifesciences Limited",
      "SubstanceName": "HYDROCHLOROTHIAZIDE; TELMISARTAN",
      "StrengthNumber": "12.5; 40",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2025-05-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "20171012",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "71335-1123-2",
      "PackageDescription": "30 CAPSULE in 1 BOTTLE (71335-1123-2) ",
      "NDC11Code": "71335-1123-02",
      "ProductNDC": "71335-1123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Minocycline Hydrochloride",
      "NonProprietaryName": "Minocycline Hydrochloride",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20080311",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA065470",
      "LabelerName": "Bryant Ranch Prepack",
      "SubstanceName": "MINOCYCLINE HYDROCHLORIDE",
      "StrengthNumber": "100",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]",
      "Status": "Active",
      "LastUpdate": "2026-03-10",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20190226",
      "SamplePackage": "N",
      "IndicationAndUsage": "Minocycline hydrochloride capsules, USP are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms.             Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae.             Respiratory tract infections caused by Mycoplasma pneumoniae.             Lymphogranuloma venereum caused by Chlamydia trachomatis.             Psittacosis (Ornithosis) due to Chlamydophila psittaci.             Trachoma caused by Chlamydia trachomatis, although the infectious agent is not always eliminated, as judged by immunofluorescence.             Inclusion conjunctivitis caused by Chlamydia trachomatis.             Nongonococcal urethritis, endocervical, or rectal infections in adults caused by Ureaplasma urealyticum or Chlamydia trachomatis.             Relapsing fever due to Borrelia recurrentis.             Chancroid caused by Haemophilus ducreyi.             Plague due to Yersinia pestis.             Tularemia due to Francisella tularensis.             Cholera caused by Vibrio cholerae.             Campylobacter fetus infections caused by Campylobacter fetus.             Brucellosis due to Brucella species (in conjunction with streptomycin).             Bartonellosis due to Bartonella bacilliformis.             Granuloma inguinale caused by Klebsiella granulomatis. Minocycline is indicated for the treatment of infections caused by the following gram-negative microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug:             Escherichia coli.            Enterobacter aerogenes.            Shigella species.            Acinetobacter species.             Respiratory tract infections caused by Haemophilus influenzae.             Respiratory tract and urinary tract infections caused by Klebsiella species. Minocycline hydrochloride capsules, USP are indicated for the treatment of infections caused by the following gram-positive microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug:             Upper respiratory tract infections caused by Streptococcus pneumoniae.             Skin and skin structure infections caused by Staphylococcus aureus. (Note: Minocycline is not the drug of choice in the treatment of any type of staphylococcal infection.). When penicillin is contraindicated, minocycline is an alternative drug in the treatment of the following infections:             Uncomplicated urethritis in men due to Neisseria gonorrhoeae and for the treatment of other gonococcal infections.             Infections in women caused by Neisseria gonorrhoeae.             Syphilis caused by Treponema pallidum subspecies pallidum.             Yaws caused by Treponema pallidum subspecies pertenue.             Listeriosis due to Listeria monocytogenes.             Anthrax due to Bacillus anthracis.             Vincent's infection caused by Fusobacterium fusiforme.             Actinomycosis caused by Actinomyces israelii.             Infections caused by Clostridium species. In acute intestinal amebiasis, minocycline may be a useful adjunct to amebicides. In severe acne, minocycline may be useful adjunctive therapy. Oral minocycline is indicated in the treatment of asymptomatic carriers of Neisseria meningitidis to eliminate meningococci from the nasopharynx. In order to preserve the usefulness of minocycline in the treatment of asymptomatic meningococcal carriers, diagnostic laboratory procedures, including serotyping and susceptibility testing, should be performed to establish the carrier state and the correct treatment. It is recommended that the prophylactic use of minocycline be reserved for situations in which the risk of meningococcal meningitis is high. Oral minocycline is not indicated for the treatment of meningococcal infection. Although no controlled clinical efficacy studies have been conducted, limited clinical data show that oral minocycline hydrochloride has been used successfully in the treatment of infections caused by Mycobacterium marinum. To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride capsules, USP and other antibacterial drugs, minocycline hydrochloride capsules, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.",
      "Description": "Minocycline hydrochloride, USP, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride. Its structural formula is. Minocycline hydrochloride capsules, USP for oral administration contain minocycline hydrochloride, USP equivalent to 50 mg, 75 mg or 100 mg of minocycline. The capsule also contains the following inactive ingredients: corn starch and magnesium stearate. The empty hard gelatin capsule shells contain titanium dioxide, sodium lauryl sulfate, and gelatin. In addition, the 50 mg capsule shells contain FD&C Red #3, D&C Red #33, and FD&C Yellow #6; the 75 mg capsule shells contain black iron oxide; and the 100 mg capsule shells contain FD&C Blue #1, D&C Red #28, FD&C Red #40, and red iron oxide. The capsules are printed with edible ink containing shellac, dehydrated alcohol, isopropyl alcohol, butyl alcohol, propylene glycol, strong ammonia solution, black iron oxide, and potassium hydroxide."
    },
    {
      "NDCCode": "72162-1123-2",
      "PackageDescription": "118 mL in 1 BOTTLE, PLASTIC (72162-1123-2) ",
      "NDC11Code": "72162-1123-02",
      "ProductNDC": "72162-1123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide",
      "NonProprietaryName": "Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide",
      "DosageFormName": "SYRUP",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150206",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA205292",
      "LabelerName": "Bryant Ranch Prepack",
      "SubstanceName": "BROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE",
      "StrengthNumber": "2; 30; 10",
      "StrengthUnit": "mg/5mL; mg/5mL; mg/5mL",
      "Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-Adrenergic Agonist [EPC]",
      "Status": "Active",
      "LastUpdate": "2025-07-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230816",
      "SamplePackage": "N",
      "IndicationAndUsage": "For relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold.",
      "Description": "Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide Syrup is a clear, light pink syrup with a butterscotch flavor. Each 5 mL (1 teaspoonful) contains. Brompheniramine Maleate, USP ................. 2 mg. Pseudoephedrine Hydrochloride, USP ........ 30 mg. Dextromethorphan Hydrobromide, USP ...... 10 mg. Alcohol 0.95% v/v. In a palatable, aromatic vehicle. Inactive Ingredients: alcohol, artificial butterscotch flavor, citric acid anhydrous, glycerin, methylparaben, propylene glycol, purified water, sodium benzoate, sodium citrate, sucrose, and FD&C Red No. 40. It may contain 10% citric acid solution or 10% sodium citrate solution for pH adjustment. The pH range is between 3.0 and 6.0. Antihistamine/Nasal Decongestant/Antitussive syrup for oral administration."
    },
    {
      "NDCCode": "73242-1123-2",
      "PackageDescription": "1 TUBE in 1 CARTON (73242-1123-2)  / 60 g in 1 TUBE (73242-1123-1) ",
      "NDC11Code": "73242-1123-02",
      "ProductNDC": "73242-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Doctrust K Tooth",
      "NonProprietaryName": "Silicon Dioxide, Sodium Monofluorophosphate",
      "DosageFormName": "GEL, DENTIFRICE",
      "RouteName": "DENTAL",
      "StartMarketingDate": "20221201",
      "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
      "LabelerName": "DONG IL PHARMS CO.,LTD",
      "SubstanceName": "SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE",
      "StrengthNumber": "16; .74",
      "StrengthUnit": "g/100g; g/100g",
      "Status": "Active",
      "LastUpdate": "2025-11-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20221201",
      "SamplePackage": "N",
      "IndicationAndUsage": "■ Helps protect against cavities."
    },
    {
      "NDCCode": "79481-1123-1",
      "PackageDescription": "2 CONTAINER in 1 CARTON (79481-1123-1)  / 40 LOZENGE in 1 CONTAINER (79481-1123-2) ",
      "NDC11Code": "79481-1123-01",
      "ProductNDC": "79481-1123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Nicotine",
      "NonProprietaryName": "Nicotine Polacrilex",
      "DosageFormName": "LOZENGE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20230615",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA077007",
      "LabelerName": "Meijer, Inc.",
      "SubstanceName": "NICOTINE",
      "StrengthNumber": "2",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]",
      "Status": "Active",
      "LastUpdate": "2025-04-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230831",
      "SamplePackage": "N",
      "IndicationAndUsage": "reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking."
    },
    {
      "NDCCode": "62795-1003-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1003-2) ",
      "NDC11Code": "62795-1003-02",
      "ProductNDC": "62795-1003",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Bodypure",
      "NonProprietaryName": ".alpha.-lipoic Acid, Avena Sativa Flowering Top, Berberis Vulgaris Root Bark, Caffeine, Cholesterol, Juglans Regia Flowering Top, Strychnos Nux-vomica Seed, Kerosene, Frangula Purshiana Bark, Ricinus Communis Seed, Solidago Virgaurea Flowering Top, Urtica Urens, Viola Tricolor, And Alcohol, X-ray Exposed (1000 Rad)",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": ".ALPHA.-LIPOIC ACID; AVENA SATIVA FLOWERING TOP; BERBERIS VULGARIS ROOT BARK; CAFFEINE; CHOLESTEROL; JUGLANS REGIA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; KEROSENE; FRANGULA PURSHIANA BARK; RICINUS COMMUNIS SEED; SOLIDAGO VIRGAUREA FLOWERING TOP; URTICA URENS; VIOLA TRICOLOR; ALCOHOL, X-RAY EXPOSED (1000 RAD)",
      "StrengthNumber": "3; 3; 6; 6; 10; 6; 30; 12; 6; 3; 4; 6; 4; 12",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-10-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20140830",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "62795-1004-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1004-2) ",
      "NDC11Code": "62795-1004-02",
      "ProductNDC": "62795-1004",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Nausea",
      "NonProprietaryName": "Semecarpus Anacardium Juice, Silver Nitrate, Activated Charcoal, Ipecac,iodine, Robinia Pseudoacacia Bark, And Sepia Officinalis Juice",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; ACTIVATED CHARCOAL; IPECAC; IODINE; ROBINIA PSEUDOACACIA BARK; SEPIA OFFICINALIS JUICE",
      "StrengthNumber": "6; 8; 12; 6; 12; 10; 30",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Active",
      "LastUpdate": "2022-12-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20221214",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor nausea, vomiting, indigestion."
    },
    {
      "NDCCode": "62795-1005-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1005-2) ",
      "NDC11Code": "62795-1005-02",
      "ProductNDC": "62795-1005",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Constipation",
      "NonProprietaryName": "Dioscorea Villosa Tuber, Sodium Chloride, And Strychnos Nux-vomica Seed",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "DIOSCOREA VILLOSA TUBER; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED",
      "StrengthNumber": "4; 200; 8",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-05-22",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    },
    {
      "NDCCode": "62795-1006-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1006-2) ",
      "NDC11Code": "62795-1006-02",
      "ProductNDC": "62795-1006",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Calming",
      "NonProprietaryName": "Matricaria Recutita, Arabica Coffee Bean, Hops, Strychnos Ignatii Seed, Moschus Moschiferus Musk Sac Resin, Strychnos Nux-vomica Seed, Passiflora Incarnata Flowering Top, Sulfur, Valerian, And Veratrum Album Root",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "MATRICARIA RECUTITA; ARABICA COFFEE BEAN; HOPS; STRYCHNOS IGNATII SEED; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; STRYCHNOS NUX-VOMICA SEED; PASSIFLORA INCARNATA FLOWERING TOP; SULFUR; VALERIAN; VERATRUM ALBUM ROOT",
      "StrengthNumber": "2; 10; 2; 8; 10; 30; 2; 12; 2; 4",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Pharm_Classes": "Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Seed Storage Proteins [CS]",
      "Status": "Active",
      "LastUpdate": "2023-08-07",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20220411",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor occassional simple nervous tension and irritability to help occassional sleeplessness."
    },
    {
      "NDCCode": "62795-1007-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1007-2) ",
      "NDC11Code": "62795-1007-02",
      "ProductNDC": "62795-1007",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Back",
      "NonProprietaryName": "Ammonium Chloride, Matricaria Recutita,citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, And Toxicodendron Pubescens Leaf",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "AMMONIUM CHLORIDE; MATRICARIA RECUTITA; CITRULLUS COLOCYNTHIS FRUIT PULP; GELSEMIUM SEMPERVIRENS ROOT; PSEUDOGNAPHALIUM OBTUSIFOLIUM; TOXICODENDRON PUBESCENS LEAF",
      "StrengthNumber": "6; 10; 5; 6; 5; 8",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Active",
      "LastUpdate": "2023-05-25",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230523",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor back pain, leg & hip pain, muscle spasm."
    },
    {
      "NDCCode": "62795-1008-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1008-2) ",
      "NDC11Code": "62795-1008-02",
      "ProductNDC": "62795-1008",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Flu Plus",
      "NonProprietaryName": "Aconitum Napellus, Cairina Moschata Heart/liver Autolysate, Bryonia Alba Whole, Eupatorium Perfoliatum Flowering Top, Ipecac, Lachesis Muta Venom,phosphorus, Pulsatilla Vulgaris, Sulfur, Zinc Gluconate, And Zinc",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "ACONITUM NAPELLUS; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; BRYONIA ALBA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; IPECAC; LACHESIS MUTA VENOM; PHOSPHORUS; PULSATILLA VULGARIS; SULFUR; ZINC GLUCONATE; ZINC",
      "StrengthNumber": "4; 200; 4; 4; 6; 12; 8; 6; 8; 3; 3",
      "StrengthUnit": "[hp_X]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-05-25",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20150101",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "62795-1009-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1009-2) ",
      "NDC11Code": "62795-1009-02",
      "ProductNDC": "62795-1009",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Arnica Plus",
      "NonProprietaryName": "Arnica Montana Root",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140930",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc.",
      "SubstanceName": "ARNICA MONTANA ROOT",
      "StrengthNumber": "6",
      "StrengthUnit": "[hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-05-21",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    },
    {
      "NDCCode": "62795-1010-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1010-2) ",
      "NDC11Code": "62795-1010-02",
      "ProductNDC": "62795-1010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Arthritis",
      "NonProprietaryName": "Arnica Montana Root, Berberis Vulgaris Root Bark, Bryonia Alba Whole, Causticum, Citrullus Colocynthis Fruit Pulp, Solanum Dulcamara Top, Ferrosoferric Phosphate, Ledum Palustre Twig, Lycopodium Clavatum Spore, Ranunculus Bulbosus, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf , And Sulfur",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "ARNICA MONTANA ROOT; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA WHOLE; CAUSTICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; SOLANUM DULCAMARA TOP; FERROSOFERRIC PHOSPHATE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; RANUNCULUS BULBOSUS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF; SULFUR",
      "StrengthNumber": "6; 8; 4; 4; 5; 6; 12; 6; 10; 8; 6; 4; 10",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Active",
      "LastUpdate": "2024-12-19",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20230523",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor arthritis pain, joint stiffness."
    },
    {
      "NDCCode": "62795-1011-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1011-2) ",
      "NDC11Code": "62795-1011-02",
      "ProductNDC": "62795-1011",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Allergy",
      "NonProprietaryName": "Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura",
      "SubstanceName": "ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT; ARNICA MONTANA ROOT; FORMIC ACID; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; PINE TAR; SELENIUM; STRYCHNOS IGNATII SEED; SULFUR; SULFURIC ACID; TELLURIUM; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "10; 8; 6; 8; 10; 8; 8; 6; 10; 12; 6; 12; 30; 10; 6",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2025-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20220411",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor allergy symptoms: runny nose, watery eyes, skin irritations."
    },
    {
      "NDCCode": "62795-1012-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1012-2) ",
      "NDC11Code": "62795-1012-02",
      "ProductNDC": "62795-1012",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Mucus Relief",
      "NonProprietaryName": "Antimony Potassium Tartrate, Atropa Belladonna, Bryonia Alba Whole, Anemone Americana, Hyoscyamus Niger, Ipecac, Lobelia Inflata, Human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "ANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA WHOLE; ANEMONE HEPATICA VAR. OBTUSA; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; LOBARIA PULMONARIA",
      "StrengthNumber": "5; 6; 6; 6; 5; 6; 4; 30; 5",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Active",
      "LastUpdate": "2022-12-16",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20221214",
      "SamplePackage": "N",
      "IndicationAndUsage": "For the temporary relief of minor chest congestion and cough due to mucus build-up."
    },
    {
      "NDCCode": "62795-1013-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1013-2) ",
      "NDC11Code": "62795-1013-02",
      "ProductNDC": "62795-1013",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Acne",
      "NonProprietaryName": "Silver Nitrate, Arnica Montana, Atropa Belladonna, Bryonia Alba Root, Solanum Dulcamara Top, Echinacea Purpurea, Calcium Sulfide, Lachesis Muta Venom, Phytolacca Americana Root, Pulsatilla Vulgaris, Rancid Beef, Toxicodendron Pubescens Leaf, And Thuja Occidentalis Leafy Twig",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20140930",
      "EndMarketingDate": "20250930",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura",
      "SubstanceName": "ARNICA MONTANA; ATROPA BELLADONNA; BRYONIA ALBA ROOT; CALCIUM SULFIDE; ECHINACEA PURPUREA; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; RANCID BEEF; SILVER NITRATE; SOLANUM DULCAMARA TOP; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF",
      "StrengthNumber": "8; 4; 5; 10; 2; 12; 6; 6; 12; 8; 6; 6; 6",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2025-10-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "StartMarketingDatePackage": "20140930",
      "EndMarketingDatePackage": "20250930",
      "SamplePackage": "N",
      "IndicationAndUsage": "Acne Relief Tablets. Relieves.  Redness.  Pain.  Tenderness."
    },
    {
      "NDCCode": "62795-1014-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1014-2) ",
      "NDC11Code": "62795-1014-02",
      "ProductNDC": "62795-1014",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Throat",
      "NonProprietaryName": "Silver Nitrate, Arnica Montana Root, Arisaema Triphyllum Root, Oyster Shell Calcium Carbonate, Crude,activated Charcoal, Causticum, Hyoscyamus Niger, Paris Quadrifolia, Phosphorus, And Verbascum Thapsus",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "SILVER NITRATE; ARNICA MONTANA ROOT; ARISAEMA TRIPHYLLUM ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; CAUSTICUM; HYOSCYAMUS NIGER; PARIS QUADRIFOLIA; PHOSPHORUS; VERBASCUM THAPSUS",
      "StrengthNumber": "6; 8; 4; 30; 10; 6; 6; 5; 10; 8",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-10-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    },
    {
      "NDCCode": "62795-1015-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1015-2) ",
      "NDC11Code": "62795-1015-02",
      "ProductNDC": "62795-1015",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Spasm Pain",
      "NonProprietaryName": "Atropine Sulfate, Aconitum Napellus, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, And Cupric Sulfate",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "ATROPINE SULFATE; ACONITUM NAPELLUS; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE",
      "StrengthNumber": "6; 4; 4; 4; 6",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-10-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    },
    {
      "NDCCode": "62795-1016-2",
      "PackageDescription": "100 TABLET in 1 PACKAGE (62795-1016-2) ",
      "NDC11Code": "62795-1016-02",
      "ProductNDC": "62795-1016",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Skin",
      "NonProprietaryName": "Berberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "BERBERIS VULGARIS ROOT BARK; GRAPHITE; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; PETROLATUM; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SULFUR",
      "StrengthNumber": "6; 10; 10; 12; 10; 8; 10; 12",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-10-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    },
    {
      "NDCCode": "62795-1017-2",
      "PackageDescription": "100 TABLET in 1 BOTTLE (62795-1017-2) ",
      "NDC11Code": "62795-1017-02",
      "ProductNDC": "62795-1017",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Bhi Sinus",
      "NonProprietaryName": "Euphorbia Resinifera Resin, Goldenseal, Potassium Dichromate, Potassium Iodide, Phosphorus, Pulsatilla Vulgaris, And Thuja Occidentalis Leafy Twig",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20150101",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "MediNatura Inc",
      "SubstanceName": "EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; POTASSIUM DICHROMATE; POTASSIUM IODIDE; PHOSPHORUS; PULSATILLA VULGARIS; THUJA OCCIDENTALIS LEAFY TWIG",
      "StrengthNumber": "6; 6; 6; 8; 8; 4; 6",
      "StrengthUnit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
      "Status": "Deprecated",
      "LastUpdate": "2021-10-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231"
    }
  ]
}
                    

{"NDC":[{"NDCCode":"62795-1123-2","ProprietaryName":"Hendel Nerve Pain Relief","NonProprietaryName":"Daphne Mezereum Bark, Arnica Montana, Arsenic Trioxide, Atropa Belladonna, Citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, Hypericum Perforatum, Ruta Graveolens Flowering Top, And Toxicodendron Pubescens Leaf"},{"NDCCode":"0008-1123-12","ProprietaryName":"Duavee","NonProprietaryName":"Conjugated Estrogens/bazedoxifene"},{"NDCCode":"17856-1123-2","ProprietaryName":"Max Relief Junior Grape","NonProprietaryName":"Childrens Acetaminophen"},{"NDCCode":"17856-1123-4","ProprietaryName":"Max Relief Junior Grape","NonProprietaryName":"Childrens Acetaminophen"},{"NDCCode":"36987-1123-2","ProprietaryName":"House Dust","NonProprietaryName":"House Dust"},{"NDCCode":"37662-1123-2","ProprietaryName":"Manganum Metallicum","NonProprietaryName":"Manganum Metallicum"},{"NDCCode":"48951-1123-2","ProprietaryName":"Arnica E Pl. Tota 2","NonProprietaryName":"Arnica E Pl. 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Arabica Coffee Bean, Hops, Strychnos Ignatii Seed, Moschus Moschiferus Musk Sac Resin, Strychnos Nux-vomica Seed, Passiflora Incarnata Flowering Top, Sulfur, Valerian, And Veratrum Album Root"},{"NDCCode":"62795-1007-2","ProprietaryName":"Bhi Back","NonProprietaryName":"Ammonium Chloride, Matricaria Recutita,citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, And Toxicodendron Pubescens Leaf"},{"NDCCode":"62795-1008-2","ProprietaryName":"Bhi Flu Plus","NonProprietaryName":"Aconitum Napellus, Cairina Moschata Heart/liver Autolysate, Bryonia Alba Whole, Eupatorium Perfoliatum Flowering Top, Ipecac, Lachesis Muta Venom,phosphorus, Pulsatilla Vulgaris, Sulfur, Zinc Gluconate, And Zinc"},{"NDCCode":"62795-1009-2","ProprietaryName":"Bhi Arnica Plus","NonProprietaryName":"Arnica Montana Root"},{"NDCCode":"62795-1010-2","ProprietaryName":"Bhi Arthritis","NonProprietaryName":"Arnica Montana Root, Berberis Vulgaris Root Bark, Bryonia Alba Whole, Causticum, Citrullus Colocynthis Fruit Pulp, Solanum Dulcamara Top, Ferrosoferric Phosphate, Ledum Palustre Twig, Lycopodium Clavatum Spore, Ranunculus Bulbosus, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf , And Sulfur"},{"NDCCode":"62795-1011-2","ProprietaryName":"Bhi Allergy","NonProprietaryName":"Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig"},{"NDCCode":"62795-1012-2","ProprietaryName":"Mucus Relief","NonProprietaryName":"Antimony Potassium Tartrate, Atropa Belladonna, Bryonia Alba Whole, Anemone Americana, Hyoscyamus Niger, Ipecac, Lobelia Inflata, Human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria"},{"NDCCode":"62795-1013-2","ProprietaryName":"Bhi Acne","NonProprietaryName":"Silver Nitrate, Arnica Montana, Atropa Belladonna, Bryonia Alba Root, Solanum Dulcamara Top, Echinacea Purpurea, Calcium Sulfide, Lachesis Muta Venom, Phytolacca Americana Root, Pulsatilla Vulgaris, Rancid Beef, Toxicodendron Pubescens Leaf, And Thuja Occidentalis Leafy Twig"},{"NDCCode":"62795-1014-2","ProprietaryName":"Bhi Throat","NonProprietaryName":"Silver Nitrate, Arnica Montana Root, Arisaema Triphyllum Root, Oyster Shell Calcium Carbonate, Crude,activated Charcoal, Causticum, Hyoscyamus Niger, Paris Quadrifolia, Phosphorus, And Verbascum Thapsus"},{"NDCCode":"62795-1015-2","ProprietaryName":"Bhi Spasm Pain","NonProprietaryName":"Atropine Sulfate, Aconitum Napellus, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, And Cupric Sulfate"},{"NDCCode":"62795-1016-2","ProprietaryName":"Bhi Skin","NonProprietaryName":"Berberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur"},{"NDCCode":"62795-1017-2","ProprietaryName":"Bhi Sinus","NonProprietaryName":"Euphorbia Resinifera Resin, Goldenseal, Potassium Dichromate, Potassium Iodide, Phosphorus, Pulsatilla Vulgaris, And Thuja Occidentalis Leafy Twig"}]}
                    

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<NDCList>
  <NDC>
    <NDCCode>62795-1123-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1123-2) </PackageDescription>
    <NDC11Code>62795-1123-02</NDC11Code>
    <ProductNDC>62795-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Hendel Nerve Pain Relief</ProprietaryName>
    <NonProprietaryName>Daphne Mezereum Bark, Arnica Montana, Arsenic Trioxide, Atropa Belladonna, Citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, Hypericum Perforatum, Ruta Graveolens Flowering Top, And Toxicodendron Pubescens Leaf</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20160801</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>DAPHNE MEZEREUM BARK; ARNICA MONTANA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM; HYPERICUM PERFORATUM; RUTA GRAVEOLENS FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF</SubstanceName>
    <StrengthNumber>3; 6; 6; 6; 6; 6; 6; 6; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-01-30</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20160801</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>0008-1123-12</NDCCode>
    <PackageDescription>1 POUCH in 1 CARTON (0008-1123-12)  / 2 BLISTER PACK in 1 POUCH / 15 TABLET, FILM COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>00008-1123-12</NDC11Code>
    <ProductNDC>0008-1123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Duavee</ProprietaryName>
    <NonProprietaryName>Conjugated Estrogens/bazedoxifene</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20131003</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA022247</ApplicationNumber>
    <LabelerName>Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.</LabelerName>
    <SubstanceName>ESTROGENS, CONJUGATED; BAZEDOXIFENE ACETATE</SubstanceName>
    <StrengthNumber>.45; 20</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Estrogen Agonist/Antagonist [EPC], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Estrogens, Conjugated (USP) [CS], Selective Estrogen Receptor Modulators [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-04-29</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20131003</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>DUAVEE is indicated in women with a uterus for.</IndicationAndUsage>
    <Description>DUAVEE (conjugated estrogens/bazedoxifene), contains conjugated estrogens with bazedoxifene, an estrogen agonist/antagonist. Conjugated estrogens are purified from pregnant mares' urine and consist of the sodium salts of water-soluble estrogen sulfates blended to represent the average composition of material derived from pregnant mares' urine. Conjugated estrogens are a mixture of sodium estrone sulfate and sodium equilin sulfate, and also contain as concomitant components, sodium sulfate conjugates, 17α-dihydroequilin, 17α-estradiol, and 17β-dihydroequilin. Bazedoxifene is supplied as the acetate salt (bazedoxifene acetate) and has the chemical name 1H-Indol-5-ol, 1-[[4-[2-(hexahydro-1H-azepin-1-yl) ethoxy]phenyl]methyl]-2-(4-hydroxyphenyl)-3-methyl-, monoacetate. The empirical formula is C30H34N2O3 ∙ C2H4O2, and the molecular weight is 530.65. Bazedoxifene acetate is a white to tan powder. The aqueous solubility of bazedoxifene is pH-dependent. Solubility is higher at lower pH. The solubility of bazedoxifene acetate in unbuffered sterile water was measured to be 923 microgramsA/mL at pH 5.4. The following represents the chemical structure of bazedoxifene acetate:. DUAVEE is available for oral administration as tablets containing 0.45 mg of conjugated estrogens with 20 mg of bazedoxifene (equivalent to 22.6 mg of bazedoxifene acetate). Each tablet of DUAVEE contains the following inactive ingredients: calcium phosphate tribasic, hydroxypropyl cellulose, microcrystalline cellulose, powdered cellulose, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol, sucrose, ascorbic acid, sucrose palmitic acid ester, hydroxyethylcellulose, titanium dioxide, red iron oxide, yellow iron oxide, black iron oxide, povidone, polydextrose, maltitol, poloxamer 188, propylene glycol, and isopropyl alcohol.</Description>
  </NDC>
  <NDC>
    <NDCCode>17856-1123-2</NDCCode>
    <PackageDescription>48 SYRINGE in 1 BOX, UNIT-DOSE (17856-1123-2)  / 5 mL in 1 SYRINGE (17856-1123-6) </PackageDescription>
    <NDC11Code>17856-1123-02</NDC11Code>
    <ProductNDC>17856-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Max Relief Junior Grape</ProprietaryName>
    <NonProprietaryName>Childrens Acetaminophen</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240701</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M013</ApplicationNumber>
    <LabelerName>ATLANTIC BIOLOGICALS CORP.</LabelerName>
    <SubstanceName>ACETAMINOPHEN</SubstanceName>
    <StrengthNumber>160</StrengthNumber>
    <StrengthUnit>mg/5mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-05-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250210</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning).</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>17856-1123-4</NDCCode>
    <PackageDescription>120 SYRINGE in 1 BOX, UNIT-DOSE (17856-1123-4)  / 2.5 mL in 1 SYRINGE (17856-1123-8) </PackageDescription>
    <NDC11Code>17856-1123-04</NDC11Code>
    <ProductNDC>17856-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Max Relief Junior Grape</ProprietaryName>
    <NonProprietaryName>Childrens Acetaminophen</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240701</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M013</ApplicationNumber>
    <LabelerName>ATLANTIC BIOLOGICALS CORP.</LabelerName>
    <SubstanceName>ACETAMINOPHEN</SubstanceName>
    <StrengthNumber>160</StrengthNumber>
    <StrengthUnit>mg/5mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-05-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20250210</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>taking the blood thinning drug warfarin. When using this product do not exceed recommended dose (see overdose warning).</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>36987-1123-2</NDCCode>
    <PackageDescription>10 mL in 1 VIAL, MULTI-DOSE (36987-1123-2)</PackageDescription>
    <NDC11Code>36987-1123-02</NDC11Code>
    <ProductNDC>36987-1123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>House Dust</ProprietaryName>
    <NonProprietaryName>House Dust</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRADERMAL; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>19720829</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA102192</ApplicationNumber>
    <LabelerName>Nelco Laboratories, Inc.</LabelerName>
    <SubstanceName>HOUSE DUST</SubstanceName>
    <StrengthNumber>10000</StrengthNumber>
    <StrengthUnit>[PNU]/mL</StrengthUnit>
    <Pharm_Classes>Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [CS],House Dust [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.</IndicationAndUsage>
    <Description>Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts). For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections.</Description>
  </NDC>
  <NDC>
    <NDCCode>37662-1123-2</NDCCode>
    <PackageDescription>1200 PELLET in 1 BOTTLE, GLASS (37662-1123-2) </PackageDescription>
    <NDC11Code>37662-1123-02</NDC11Code>
    <ProductNDC>37662-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Manganum Metallicum</ProprietaryName>
    <NonProprietaryName>Manganum Metallicum</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20220801</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Hahnemann Laboratories, INC.</LabelerName>
    <SubstanceName>MANGANESE</SubstanceName>
    <StrengthNumber>6</StrengthNumber>
    <StrengthUnit>[hp_C]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2022-08-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220801</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>48951-1123-2</NDCCode>
    <PackageDescription>1350 PELLET in 1 BOTTLE, GLASS (48951-1123-2) </PackageDescription>
    <NDC11Code>48951-1123-02</NDC11Code>
    <ProductNDC>48951-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Arnica E Pl. Tota 2</ProprietaryName>
    <NonProprietaryName>Arnica E Pl. Tota 2</NonProprietaryName>
    <DosageFormName>PELLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20090901</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Uriel Pharmacy Inc.</LabelerName>
    <SubstanceName>ARNICA MONTANA</SubstanceName>
    <StrengthNumber>2</StrengthNumber>
    <StrengthUnit>[hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2020-11-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20090901</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>62699-1123-2</NDCCode>
    <PackageDescription>12 BOX in 1 BOX (62699-1123-2)  &gt; 1 TUBE in 1 BOX &gt; 50 g in 1 TUBE</PackageDescription>
    <NDC11Code>62699-1123-02</NDC11Code>
    <ProductNDC>62699-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Golden Sunshine Herbal</ProprietaryName>
    <NonProprietaryName>Topical Analgesic</NonProprietaryName>
    <DosageFormName>CREAM</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20100615</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part348</ApplicationNumber>
    <LabelerName>Nan Mei Pharmaceutical Co., Ltd.</LabelerName>
    <SubstanceName>MENTHOL; METHYL SALICYLATE</SubstanceName>
    <StrengthNumber>.02; .005</StrengthNumber>
    <StrengthUnit>g/g; g/g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62991-1123-2</NDCCode>
    <PackageDescription>100 g in 1 JAR (62991-1123-2) </PackageDescription>
    <NDC11Code>62991-1123-02</NDC11Code>
    <ProductNDC>62991-1123</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Progesterone Wettable</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20090623</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING</MarketingCategoryName>
    <LabelerName>LETCO MEDICAL, LLC</LabelerName>
    <SubstanceName>PROGESTERONE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>g/g</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2026-04-09</LastUpdate>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>23-JUN-09</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>64942-1123-2</NDCCode>
    <PackageDescription>12 g in 1 CONTAINER (64942-1123-2)</PackageDescription>
    <NDC11Code>64942-1123-02</NDC11Code>
    <ProductNDC>64942-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Dove Men Plus Care</ProprietaryName>
    <ProprietaryNameSuffix>Clean Comfort Antiperspirant And Deodorant</ProprietaryNameSuffix>
    <NonProprietaryName>Aluminum Zirconium Tetrachlorohydrex Gly</NonProprietaryName>
    <DosageFormName>STICK</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20101006</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
    <ApplicationNumber>part350</ApplicationNumber>
    <LabelerName>Conopco Inc. d/b/a Unilever</LabelerName>
    <SubstanceName>ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY</SubstanceName>
    <StrengthNumber>14.8</StrengthNumber>
    <StrengthUnit>g/100g</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>70771-1123-8</NDCCode>
    <PackageDescription>3 BLISTER PACK in 1 CARTON (70771-1123-8)  &gt; 10 TABLET in 1 BLISTER PACK (70771-1123-2) </PackageDescription>
    <NDC11Code>70771-1123-08</NDC11Code>
    <ProductNDC>70771-1123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Telmisartan And Hydrochlorothiazide</ProprietaryName>
    <NonProprietaryName>Telmisartan And Hydrochlorothiazide</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20171012</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA204221</ApplicationNumber>
    <LabelerName>Zydus Lifesciences Limited</LabelerName>
    <SubstanceName>HYDROCHLOROTHIAZIDE; TELMISARTAN</SubstanceName>
    <StrengthNumber>12.5; 40</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2025-05-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171012</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>71335-1123-2</NDCCode>
    <PackageDescription>30 CAPSULE in 1 BOTTLE (71335-1123-2) </PackageDescription>
    <NDC11Code>71335-1123-02</NDC11Code>
    <ProductNDC>71335-1123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Minocycline Hydrochloride</ProprietaryName>
    <NonProprietaryName>Minocycline Hydrochloride</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20080311</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA065470</ApplicationNumber>
    <LabelerName>Bryant Ranch Prepack</LabelerName>
    <SubstanceName>MINOCYCLINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>100</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-03-10</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20190226</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Minocycline hydrochloride capsules, USP are indicated in the treatment of the following infections due to susceptible strains of the designated microorganisms.             Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox and tick fevers caused by rickettsiae.             Respiratory tract infections caused by Mycoplasma pneumoniae.             Lymphogranuloma venereum caused by Chlamydia trachomatis.             Psittacosis (Ornithosis) due to Chlamydophila psittaci.             Trachoma caused by Chlamydia trachomatis, although the infectious agent is not always eliminated, as judged by immunofluorescence.             Inclusion conjunctivitis caused by Chlamydia trachomatis.             Nongonococcal urethritis, endocervical, or rectal infections in adults caused by Ureaplasma urealyticum or Chlamydia trachomatis.             Relapsing fever due to Borrelia recurrentis.             Chancroid caused by Haemophilus ducreyi.             Plague due to Yersinia pestis.             Tularemia due to Francisella tularensis.             Cholera caused by Vibrio cholerae.             Campylobacter fetus infections caused by Campylobacter fetus.             Brucellosis due to Brucella species (in conjunction with streptomycin).             Bartonellosis due to Bartonella bacilliformis.             Granuloma inguinale caused by Klebsiella granulomatis. Minocycline is indicated for the treatment of infections caused by the following gram-negative microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug:             Escherichia coli.            Enterobacter aerogenes.            Shigella species.            Acinetobacter species.             Respiratory tract infections caused by Haemophilus influenzae.             Respiratory tract and urinary tract infections caused by Klebsiella species. Minocycline hydrochloride capsules, USP are indicated for the treatment of infections caused by the following gram-positive microorganisms when bacteriologic testing indicates appropriate susceptibility to the drug:             Upper respiratory tract infections caused by Streptococcus pneumoniae.             Skin and skin structure infections caused by Staphylococcus aureus. (Note: Minocycline is not the drug of choice in the treatment of any type of staphylococcal infection.). When penicillin is contraindicated, minocycline is an alternative drug in the treatment of the following infections:             Uncomplicated urethritis in men due to Neisseria gonorrhoeae and for the treatment of other gonococcal infections.             Infections in women caused by Neisseria gonorrhoeae.             Syphilis caused by Treponema pallidum subspecies pallidum.             Yaws caused by Treponema pallidum subspecies pertenue.             Listeriosis due to Listeria monocytogenes.             Anthrax due to Bacillus anthracis.             Vincent's infection caused by Fusobacterium fusiforme.             Actinomycosis caused by Actinomyces israelii.             Infections caused by Clostridium species. In acute intestinal amebiasis, minocycline may be a useful adjunct to amebicides. In severe acne, minocycline may be useful adjunctive therapy. Oral minocycline is indicated in the treatment of asymptomatic carriers of Neisseria meningitidis to eliminate meningococci from the nasopharynx. In order to preserve the usefulness of minocycline in the treatment of asymptomatic meningococcal carriers, diagnostic laboratory procedures, including serotyping and susceptibility testing, should be performed to establish the carrier state and the correct treatment. It is recommended that the prophylactic use of minocycline be reserved for situations in which the risk of meningococcal meningitis is high. Oral minocycline is not indicated for the treatment of meningococcal infection. Although no controlled clinical efficacy studies have been conducted, limited clinical data show that oral minocycline hydrochloride has been used successfully in the treatment of infections caused by Mycobacterium marinum. To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride capsules, USP and other antibacterial drugs, minocycline hydrochloride capsules, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.</IndicationAndUsage>
    <Description>Minocycline hydrochloride, USP, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride. Its structural formula is. Minocycline hydrochloride capsules, USP for oral administration contain minocycline hydrochloride, USP equivalent to 50 mg, 75 mg or 100 mg of minocycline. The capsule also contains the following inactive ingredients: corn starch and magnesium stearate. The empty hard gelatin capsule shells contain titanium dioxide, sodium lauryl sulfate, and gelatin. In addition, the 50 mg capsule shells contain FD&amp;C Red #3, D&amp;C Red #33, and FD&amp;C Yellow #6; the 75 mg capsule shells contain black iron oxide; and the 100 mg capsule shells contain FD&amp;C Blue #1, D&amp;C Red #28, FD&amp;C Red #40, and red iron oxide. The capsules are printed with edible ink containing shellac, dehydrated alcohol, isopropyl alcohol, butyl alcohol, propylene glycol, strong ammonia solution, black iron oxide, and potassium hydroxide.</Description>
  </NDC>
  <NDC>
    <NDCCode>72162-1123-2</NDCCode>
    <PackageDescription>118 mL in 1 BOTTLE, PLASTIC (72162-1123-2) </PackageDescription>
    <NDC11Code>72162-1123-02</NDC11Code>
    <ProductNDC>72162-1123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide</ProprietaryName>
    <NonProprietaryName>Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide</NonProprietaryName>
    <DosageFormName>SYRUP</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150206</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA205292</ApplicationNumber>
    <LabelerName>Bryant Ranch Prepack</LabelerName>
    <SubstanceName>BROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE</SubstanceName>
    <StrengthNumber>2; 30; 10</StrengthNumber>
    <StrengthUnit>mg/5mL; mg/5mL; mg/5mL</StrengthUnit>
    <Pharm_Classes>Adrenergic alpha-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-07-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230816</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold.</IndicationAndUsage>
    <Description>Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide Syrup is a clear, light pink syrup with a butterscotch flavor. Each 5 mL (1 teaspoonful) contains. Brompheniramine Maleate, USP ................. 2 mg. Pseudoephedrine Hydrochloride, USP ........ 30 mg. Dextromethorphan Hydrobromide, USP ...... 10 mg. Alcohol 0.95% v/v. In a palatable, aromatic vehicle. Inactive Ingredients: alcohol, artificial butterscotch flavor, citric acid anhydrous, glycerin, methylparaben, propylene glycol, purified water, sodium benzoate, sodium citrate, sucrose, and FD&amp;C Red No. 40. It may contain 10% citric acid solution or 10% sodium citrate solution for pH adjustment. The pH range is between 3.0 and 6.0. Antihistamine/Nasal Decongestant/Antitussive syrup for oral administration.</Description>
  </NDC>
  <NDC>
    <NDCCode>73242-1123-2</NDCCode>
    <PackageDescription>1 TUBE in 1 CARTON (73242-1123-2)  / 60 g in 1 TUBE (73242-1123-1) </PackageDescription>
    <NDC11Code>73242-1123-02</NDC11Code>
    <ProductNDC>73242-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Doctrust K Tooth</ProprietaryName>
    <NonProprietaryName>Silicon Dioxide, Sodium Monofluorophosphate</NonProprietaryName>
    <DosageFormName>GEL, DENTIFRICE</DosageFormName>
    <RouteName>DENTAL</RouteName>
    <StartMarketingDate>20221201</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED DRUG OTHER</MarketingCategoryName>
    <LabelerName>DONG IL PHARMS CO.,LTD</LabelerName>
    <SubstanceName>SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE</SubstanceName>
    <StrengthNumber>16; .74</StrengthNumber>
    <StrengthUnit>g/100g; g/100g</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2025-11-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20221201</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>■ Helps protect against cavities.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>79481-1123-1</NDCCode>
    <PackageDescription>2 CONTAINER in 1 CARTON (79481-1123-1)  / 40 LOZENGE in 1 CONTAINER (79481-1123-2) </PackageDescription>
    <NDC11Code>79481-1123-01</NDC11Code>
    <ProductNDC>79481-1123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Nicotine</ProprietaryName>
    <NonProprietaryName>Nicotine Polacrilex</NonProprietaryName>
    <DosageFormName>LOZENGE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20230615</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA077007</ApplicationNumber>
    <LabelerName>Meijer, Inc.</LabelerName>
    <SubstanceName>NICOTINE</SubstanceName>
    <StrengthNumber>2</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Cholinergic Nicotinic Agonist [EPC], Nicotine [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-04-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230831</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>reduces withdrawal symptoms, including nicotine craving, associated with quitting smoking.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1003-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1003-2) </PackageDescription>
    <NDC11Code>62795-1003-02</NDC11Code>
    <ProductNDC>62795-1003</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Bodypure</ProprietaryName>
    <NonProprietaryName>.alpha.-lipoic Acid, Avena Sativa Flowering Top, Berberis Vulgaris Root Bark, Caffeine, Cholesterol, Juglans Regia Flowering Top, Strychnos Nux-vomica Seed, Kerosene, Frangula Purshiana Bark, Ricinus Communis Seed, Solidago Virgaurea Flowering Top, Urtica Urens, Viola Tricolor, And Alcohol, X-ray Exposed (1000 Rad)</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>.ALPHA.-LIPOIC ACID; AVENA SATIVA FLOWERING TOP; BERBERIS VULGARIS ROOT BARK; CAFFEINE; CHOLESTEROL; JUGLANS REGIA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; KEROSENE; FRANGULA PURSHIANA BARK; RICINUS COMMUNIS SEED; SOLIDAGO VIRGAUREA FLOWERING TOP; URTICA URENS; VIOLA TRICOLOR; ALCOHOL, X-RAY EXPOSED (1000 RAD)</SubstanceName>
    <StrengthNumber>3; 3; 6; 6; 10; 6; 30; 12; 6; 3; 4; 6; 4; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-10-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20140830</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>62795-1004-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1004-2) </PackageDescription>
    <NDC11Code>62795-1004-02</NDC11Code>
    <ProductNDC>62795-1004</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Nausea</ProprietaryName>
    <NonProprietaryName>Semecarpus Anacardium Juice, Silver Nitrate, Activated Charcoal, Ipecac,iodine, Robinia Pseudoacacia Bark, And Sepia Officinalis Juice</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; ACTIVATED CHARCOAL; IPECAC; IODINE; ROBINIA PSEUDOACACIA BARK; SEPIA OFFICINALIS JUICE</SubstanceName>
    <StrengthNumber>6; 8; 12; 6; 12; 10; 30</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2022-12-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20221214</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor nausea, vomiting, indigestion.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1005-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1005-2) </PackageDescription>
    <NDC11Code>62795-1005-02</NDC11Code>
    <ProductNDC>62795-1005</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Constipation</ProprietaryName>
    <NonProprietaryName>Dioscorea Villosa Tuber, Sodium Chloride, And Strychnos Nux-vomica Seed</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>DIOSCOREA VILLOSA TUBER; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED</SubstanceName>
    <StrengthNumber>4; 200; 8</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-05-22</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62795-1006-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1006-2) </PackageDescription>
    <NDC11Code>62795-1006-02</NDC11Code>
    <ProductNDC>62795-1006</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Calming</ProprietaryName>
    <NonProprietaryName>Matricaria Recutita, Arabica Coffee Bean, Hops, Strychnos Ignatii Seed, Moschus Moschiferus Musk Sac Resin, Strychnos Nux-vomica Seed, Passiflora Incarnata Flowering Top, Sulfur, Valerian, And Veratrum Album Root</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>MATRICARIA RECUTITA; ARABICA COFFEE BEAN; HOPS; STRYCHNOS IGNATII SEED; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; STRYCHNOS NUX-VOMICA SEED; PASSIFLORA INCARNATA FLOWERING TOP; SULFUR; VALERIAN; VERATRUM ALBUM ROOT</SubstanceName>
    <StrengthNumber>2; 10; 2; 8; 10; 30; 2; 12; 2; 4</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Pharm_Classes>Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2023-08-07</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220411</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor occassional simple nervous tension and irritability to help occassional sleeplessness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1007-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1007-2) </PackageDescription>
    <NDC11Code>62795-1007-02</NDC11Code>
    <ProductNDC>62795-1007</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Back</ProprietaryName>
    <NonProprietaryName>Ammonium Chloride, Matricaria Recutita,citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, And Toxicodendron Pubescens Leaf</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>AMMONIUM CHLORIDE; MATRICARIA RECUTITA; CITRULLUS COLOCYNTHIS FRUIT PULP; GELSEMIUM SEMPERVIRENS ROOT; PSEUDOGNAPHALIUM OBTUSIFOLIUM; TOXICODENDRON PUBESCENS LEAF</SubstanceName>
    <StrengthNumber>6; 10; 5; 6; 5; 8</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2023-05-25</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230523</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor back pain, leg &amp; hip pain, muscle spasm.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1008-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1008-2) </PackageDescription>
    <NDC11Code>62795-1008-02</NDC11Code>
    <ProductNDC>62795-1008</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Flu Plus</ProprietaryName>
    <NonProprietaryName>Aconitum Napellus, Cairina Moschata Heart/liver Autolysate, Bryonia Alba Whole, Eupatorium Perfoliatum Flowering Top, Ipecac, Lachesis Muta Venom,phosphorus, Pulsatilla Vulgaris, Sulfur, Zinc Gluconate, And Zinc</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE; BRYONIA ALBA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; IPECAC; LACHESIS MUTA VENOM; PHOSPHORUS; PULSATILLA VULGARIS; SULFUR; ZINC GLUCONATE; ZINC</SubstanceName>
    <StrengthNumber>4; 200; 4; 4; 6; 12; 8; 6; 8; 3; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_C]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-05-25</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20150101</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>62795-1009-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1009-2) </PackageDescription>
    <NDC11Code>62795-1009-02</NDC11Code>
    <ProductNDC>62795-1009</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Arnica Plus</ProprietaryName>
    <NonProprietaryName>Arnica Montana Root</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140930</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc.</LabelerName>
    <SubstanceName>ARNICA MONTANA ROOT</SubstanceName>
    <StrengthNumber>6</StrengthNumber>
    <StrengthUnit>[hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-05-21</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62795-1010-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1010-2) </PackageDescription>
    <NDC11Code>62795-1010-02</NDC11Code>
    <ProductNDC>62795-1010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Arthritis</ProprietaryName>
    <NonProprietaryName>Arnica Montana Root, Berberis Vulgaris Root Bark, Bryonia Alba Whole, Causticum, Citrullus Colocynthis Fruit Pulp, Solanum Dulcamara Top, Ferrosoferric Phosphate, Ledum Palustre Twig, Lycopodium Clavatum Spore, Ranunculus Bulbosus, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf , And Sulfur</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>ARNICA MONTANA ROOT; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA WHOLE; CAUSTICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; SOLANUM DULCAMARA TOP; FERROSOFERRIC PHOSPHATE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; RANUNCULUS BULBOSUS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF; SULFUR</SubstanceName>
    <StrengthNumber>6; 8; 4; 4; 5; 6; 12; 6; 10; 8; 6; 4; 10</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2024-12-19</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230523</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor arthritis pain, joint stiffness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1011-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1011-2) </PackageDescription>
    <NDC11Code>62795-1011-02</NDC11Code>
    <ProductNDC>62795-1011</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Allergy</ProprietaryName>
    <NonProprietaryName>Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura</LabelerName>
    <SubstanceName>ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT; ARNICA MONTANA ROOT; FORMIC ACID; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; PINE TAR; SELENIUM; STRYCHNOS IGNATII SEED; SULFUR; SULFURIC ACID; TELLURIUM; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>10; 8; 6; 8; 10; 8; 8; 6; 10; 12; 6; 12; 30; 10; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2025-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20220411</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor allergy symptoms: runny nose, watery eyes, skin irritations.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1012-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1012-2) </PackageDescription>
    <NDC11Code>62795-1012-02</NDC11Code>
    <ProductNDC>62795-1012</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Mucus Relief</ProprietaryName>
    <NonProprietaryName>Antimony Potassium Tartrate, Atropa Belladonna, Bryonia Alba Whole, Anemone Americana, Hyoscyamus Niger, Ipecac, Lobelia Inflata, Human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>ANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA WHOLE; ANEMONE HEPATICA VAR. OBTUSA; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; LOBARIA PULMONARIA</SubstanceName>
    <StrengthNumber>5; 6; 6; 6; 5; 6; 4; 30; 5</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2022-12-16</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20221214</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>For the temporary relief of minor chest congestion and cough due to mucus build-up.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1013-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1013-2) </PackageDescription>
    <NDC11Code>62795-1013-02</NDC11Code>
    <ProductNDC>62795-1013</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Acne</ProprietaryName>
    <NonProprietaryName>Silver Nitrate, Arnica Montana, Atropa Belladonna, Bryonia Alba Root, Solanum Dulcamara Top, Echinacea Purpurea, Calcium Sulfide, Lachesis Muta Venom, Phytolacca Americana Root, Pulsatilla Vulgaris, Rancid Beef, Toxicodendron Pubescens Leaf, And Thuja Occidentalis Leafy Twig</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20140930</StartMarketingDate>
    <EndMarketingDate>20250930</EndMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura</LabelerName>
    <SubstanceName>ARNICA MONTANA; ATROPA BELLADONNA; BRYONIA ALBA ROOT; CALCIUM SULFIDE; ECHINACEA PURPUREA; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; RANCID BEEF; SILVER NITRATE; SOLANUM DULCAMARA TOP; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF</SubstanceName>
    <StrengthNumber>8; 4; 5; 10; 2; 12; 6; 6; 12; 8; 6; 6; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2025-10-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <StartMarketingDatePackage>20140930</StartMarketingDatePackage>
    <EndMarketingDatePackage>20250930</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Acne Relief Tablets. Relieves.  Redness.  Pain.  Tenderness.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62795-1014-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1014-2) </PackageDescription>
    <NDC11Code>62795-1014-02</NDC11Code>
    <ProductNDC>62795-1014</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Throat</ProprietaryName>
    <NonProprietaryName>Silver Nitrate, Arnica Montana Root, Arisaema Triphyllum Root, Oyster Shell Calcium Carbonate, Crude,activated Charcoal, Causticum, Hyoscyamus Niger, Paris Quadrifolia, Phosphorus, And Verbascum Thapsus</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>SILVER NITRATE; ARNICA MONTANA ROOT; ARISAEMA TRIPHYLLUM ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; CAUSTICUM; HYOSCYAMUS NIGER; PARIS QUADRIFOLIA; PHOSPHORUS; VERBASCUM THAPSUS</SubstanceName>
    <StrengthNumber>6; 8; 4; 30; 10; 6; 6; 5; 10; 8</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-10-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62795-1015-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1015-2) </PackageDescription>
    <NDC11Code>62795-1015-02</NDC11Code>
    <ProductNDC>62795-1015</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Spasm Pain</ProprietaryName>
    <NonProprietaryName>Atropine Sulfate, Aconitum Napellus, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, And Cupric Sulfate</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>ATROPINE SULFATE; ACONITUM NAPELLUS; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE</SubstanceName>
    <StrengthNumber>6; 4; 4; 4; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-10-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62795-1016-2</NDCCode>
    <PackageDescription>100 TABLET in 1 PACKAGE (62795-1016-2) </PackageDescription>
    <NDC11Code>62795-1016-02</NDC11Code>
    <ProductNDC>62795-1016</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Skin</ProprietaryName>
    <NonProprietaryName>Berberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>BERBERIS VULGARIS ROOT BARK; GRAPHITE; HYDROFLUORIC ACID; LYCOPODIUM CLAVATUM SPORE; PETROLATUM; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SULFUR</SubstanceName>
    <StrengthNumber>6; 10; 10; 12; 10; 8; 10; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-10-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>62795-1017-2</NDCCode>
    <PackageDescription>100 TABLET in 1 BOTTLE (62795-1017-2) </PackageDescription>
    <NDC11Code>62795-1017-02</NDC11Code>
    <ProductNDC>62795-1017</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Bhi Sinus</ProprietaryName>
    <NonProprietaryName>Euphorbia Resinifera Resin, Goldenseal, Potassium Dichromate, Potassium Iodide, Phosphorus, Pulsatilla Vulgaris, And Thuja Occidentalis Leafy Twig</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20150101</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>MediNatura Inc</LabelerName>
    <SubstanceName>EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; POTASSIUM DICHROMATE; POTASSIUM IODIDE; PHOSPHORUS; PULSATILLA VULGARIS; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
    <StrengthNumber>6; 6; 6; 8; 8; 4; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-10-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>62795-1123-2</NDCCode><ProprietaryName>Hendel Nerve Pain Relief</ProprietaryName><NonProprietaryName>Daphne Mezereum Bark, Arnica Montana, Arsenic Trioxide, Atropa Belladonna, Citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, Hypericum Perforatum, Ruta Graveolens Flowering Top, And Toxicodendron Pubescens Leaf</NonProprietaryName></NDC><NDC><NDCCode>0008-1123-12</NDCCode><ProprietaryName>Duavee</ProprietaryName><NonProprietaryName>Conjugated Estrogens/bazedoxifene</NonProprietaryName></NDC><NDC><NDCCode>17856-1123-2</NDCCode><ProprietaryName>Max Relief Junior Grape</ProprietaryName><NonProprietaryName>Childrens Acetaminophen</NonProprietaryName></NDC><NDC><NDCCode>17856-1123-4</NDCCode><ProprietaryName>Max Relief Junior Grape</ProprietaryName><NonProprietaryName>Childrens Acetaminophen</NonProprietaryName></NDC><NDC><NDCCode>36987-1123-2</NDCCode><ProprietaryName>House Dust</ProprietaryName><NonProprietaryName>House Dust</NonProprietaryName></NDC><NDC><NDCCode>37662-1123-2</NDCCode><ProprietaryName>Manganum Metallicum</ProprietaryName><NonProprietaryName>Manganum Metallicum</NonProprietaryName></NDC><NDC><NDCCode>48951-1123-2</NDCCode><ProprietaryName>Arnica E Pl. Tota 2</ProprietaryName><NonProprietaryName>Arnica E Pl. Tota 2</NonProprietaryName></NDC><NDC><NDCCode>62699-1123-2</NDCCode><ProprietaryName>Golden Sunshine Herbal</ProprietaryName><NonProprietaryName>Topical Analgesic</NonProprietaryName></NDC><NDC><NDCCode>62991-1123-2</NDCCode><NonProprietaryName>Progesterone Wettable</NonProprietaryName></NDC><NDC><NDCCode>64942-1123-2</NDCCode><ProprietaryName>Dove Men Plus Care</ProprietaryName><NonProprietaryName>Aluminum Zirconium Tetrachlorohydrex Gly</NonProprietaryName></NDC><NDC><NDCCode>70771-1123-8</NDCCode><ProprietaryName>Telmisartan And Hydrochlorothiazide</ProprietaryName><NonProprietaryName>Telmisartan And Hydrochlorothiazide</NonProprietaryName></NDC><NDC><NDCCode>71335-1123-2</NDCCode><ProprietaryName>Minocycline Hydrochloride</ProprietaryName><NonProprietaryName>Minocycline Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>72162-1123-2</NDCCode><ProprietaryName>Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide</ProprietaryName><NonProprietaryName>Brompheniramine Maleate, Pseudoephedrine Hydrochloride And Dextromethorphan Hydrobromide</NonProprietaryName></NDC><NDC><NDCCode>73242-1123-2</NDCCode><ProprietaryName>Doctrust K Tooth</ProprietaryName><NonProprietaryName>Silicon Dioxide, Sodium Monofluorophosphate</NonProprietaryName></NDC><NDC><NDCCode>79481-1123-1</NDCCode><ProprietaryName>Nicotine</ProprietaryName><NonProprietaryName>Nicotine Polacrilex</NonProprietaryName></NDC><NDC><NDCCode>62795-1003-2</NDCCode><ProprietaryName>Bhi Bodypure</ProprietaryName><NonProprietaryName>.alpha.-lipoic Acid, Avena Sativa Flowering Top, Berberis Vulgaris Root Bark, Caffeine, Cholesterol, Juglans Regia Flowering Top, Strychnos Nux-vomica Seed, Kerosene, Frangula Purshiana Bark, Ricinus Communis Seed, Solidago Virgaurea Flowering Top, Urtica Urens, Viola Tricolor, And Alcohol, X-ray Exposed (1000 Rad)</NonProprietaryName></NDC><NDC><NDCCode>62795-1004-2</NDCCode><ProprietaryName>Bhi Nausea</ProprietaryName><NonProprietaryName>Semecarpus Anacardium Juice, Silver Nitrate, Activated Charcoal, Ipecac,iodine, Robinia Pseudoacacia Bark, And Sepia Officinalis Juice</NonProprietaryName></NDC><NDC><NDCCode>62795-1005-2</NDCCode><ProprietaryName>Bhi Constipation</ProprietaryName><NonProprietaryName>Dioscorea Villosa Tuber, Sodium Chloride, And Strychnos Nux-vomica Seed</NonProprietaryName></NDC><NDC><NDCCode>62795-1006-2</NDCCode><ProprietaryName>Bhi Calming</ProprietaryName><NonProprietaryName>Matricaria Recutita, Arabica Coffee Bean, Hops, Strychnos Ignatii Seed, Moschus Moschiferus Musk Sac Resin, Strychnos Nux-vomica Seed, Passiflora Incarnata Flowering Top, Sulfur, Valerian, And Veratrum Album Root</NonProprietaryName></NDC><NDC><NDCCode>62795-1007-2</NDCCode><ProprietaryName>Bhi Back</ProprietaryName><NonProprietaryName>Ammonium Chloride, Matricaria Recutita,citrullus Colocynthis Fruit Pulp, Pseudognaphalium Obtusifolium, And Toxicodendron Pubescens Leaf</NonProprietaryName></NDC><NDC><NDCCode>62795-1008-2</NDCCode><ProprietaryName>Bhi Flu Plus</ProprietaryName><NonProprietaryName>Aconitum Napellus, Cairina Moschata Heart/liver Autolysate, Bryonia Alba Whole, Eupatorium Perfoliatum Flowering Top, Ipecac, Lachesis Muta Venom,phosphorus, Pulsatilla Vulgaris, Sulfur, Zinc Gluconate, And Zinc</NonProprietaryName></NDC><NDC><NDCCode>62795-1009-2</NDCCode><ProprietaryName>Bhi Arnica Plus</ProprietaryName><NonProprietaryName>Arnica Montana Root</NonProprietaryName></NDC><NDC><NDCCode>62795-1010-2</NDCCode><ProprietaryName>Bhi Arthritis</ProprietaryName><NonProprietaryName>Arnica Montana Root, Berberis Vulgaris Root Bark, Bryonia Alba Whole, Causticum, Citrullus Colocynthis Fruit Pulp, Solanum Dulcamara Top, Ferrosoferric Phosphate, Ledum Palustre Twig, Lycopodium Clavatum Spore, Ranunculus Bulbosus, Rhododendron Aureum Leaf, Toxicodendron Pubescens Leaf , And Sulfur</NonProprietaryName></NDC><NDC><NDCCode>62795-1011-2</NDCCode><ProprietaryName>Bhi Allergy</ProprietaryName><NonProprietaryName>Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig</NonProprietaryName></NDC><NDC><NDCCode>62795-1012-2</NDCCode><ProprietaryName>Mucus Relief</ProprietaryName><NonProprietaryName>Antimony Potassium Tartrate, Atropa Belladonna, Bryonia Alba Whole, Anemone Americana, Hyoscyamus Niger, Ipecac, Lobelia Inflata, Human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria</NonProprietaryName></NDC><NDC><NDCCode>62795-1013-2</NDCCode><ProprietaryName>Bhi Acne</ProprietaryName><NonProprietaryName>Silver Nitrate, Arnica Montana, Atropa Belladonna, Bryonia Alba Root, Solanum Dulcamara Top, Echinacea Purpurea, Calcium Sulfide, Lachesis Muta Venom, Phytolacca Americana Root, Pulsatilla Vulgaris, Rancid Beef, Toxicodendron Pubescens Leaf, And Thuja Occidentalis Leafy Twig</NonProprietaryName></NDC><NDC><NDCCode>62795-1014-2</NDCCode><ProprietaryName>Bhi Throat</ProprietaryName><NonProprietaryName>Silver Nitrate, Arnica Montana Root, Arisaema Triphyllum Root, Oyster Shell Calcium Carbonate, Crude,activated Charcoal, Causticum, Hyoscyamus Niger, Paris Quadrifolia, Phosphorus, And Verbascum Thapsus</NonProprietaryName></NDC><NDC><NDCCode>62795-1015-2</NDCCode><ProprietaryName>Bhi Spasm Pain</ProprietaryName><NonProprietaryName>Atropine Sulfate, Aconitum Napellus, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, And Cupric Sulfate</NonProprietaryName></NDC><NDC><NDCCode>62795-1016-2</NDCCode><ProprietaryName>Bhi Skin</ProprietaryName><NonProprietaryName>Berberis Vulgaris Root Bark, Graphite, Hydrofluoric Acid, Lycopodium Clavatum Spore, Petrolatum, Toxicodendron Pubescens Leaf, Sepia Officinalis Juice, And Sulfur</NonProprietaryName></NDC><NDC><NDCCode>62795-1017-2</NDCCode><ProprietaryName>Bhi Sinus</ProprietaryName><NonProprietaryName>Euphorbia Resinifera Resin, Goldenseal, Potassium Dichromate, Potassium Iodide, Phosphorus, Pulsatilla Vulgaris, And Thuja Occidentalis Leafy Twig</NonProprietaryName></NDC></NDCList>
                    

Using REST to Invoke DataLabs API

Introduction

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

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

Working With DataLabs REST API

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

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

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

Four parameters are required with each “search” request:

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

Optional parameter:

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

All other query parameters (if any) are optional.

Full list of API parameters:

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

Operations Currently Available in the DataLabs REST API

Currently DataLabs RESTful Lookup Service supports following operations:

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

Plus there are three NPI-specific operations:

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

REST Search Examples

Query Parameter Reference

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

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

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

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

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

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

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

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

        Console.WriteLine(response);

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

            
{
  "NPI": [
    {
      "NPI": "1295783033",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "REDMOND EYE DOCTORS, PLLC",
      "FirstLineMailingAddress": "16375 NE 85TH ST",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3554",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-7363",
      "MailingAddressFaxNumber": "425-861-5585",
      "FirstLinePracticeLocationAddress": "16375 NE 85TH ST",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3554",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-7363",
      "PracticeLocationAddressFaxNumber": "425-861-5585",
      "EnumerationDate": "05/04/2006",
      "LastUpdateDate": "12/11/2007",
      "AuthorizedOfficialLastName": "MONTECILLO",
      "AuthorizedOfficialFirstName": "RANIA",
      "AuthorizedOfficialTitle": "OWNER",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "O.D.",
      "AuthorizedOfficialTelephoneNumber": "425-885-7363",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "801TX",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization."
    },
    {
      "NPI": "1346319878",
      "EntityType": "Organization",
      "EIN": "N/A",
      "OrgName": "REDMOND EYE CLINIC PLLC",
      "FirstLineMailingAddress": "16150 NE 85TH ST STE 206",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3543",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-3574",
      "MailingAddressFaxNumber": "425-881-0230",
      "FirstLinePracticeLocationAddress": "16150 NE 85TH ST STE 206",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3543",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-3574",
      "PracticeLocationAddressFaxNumber": "425-881-0230",
      "EnumerationDate": "11/07/2006",
      "LastUpdateDate": "07/08/2007",
      "AuthorizedOfficialLastName": "OTTEN",
      "AuthorizedOfficialFirstName": "LARRY",
      "AuthorizedOfficialMiddleName": "C",
      "AuthorizedOfficialTitle": "DR",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "O.D.",
      "AuthorizedOfficialTelephoneNumber": "425-885-3574",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "OD00001172",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193200000X MULTI-SPECIALTY GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization."
    },
    {
      "NPI": "1376755009",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "PERIMAN",
      "FirstName": "LAURA",
      "MiddleName": "MARIE",
      "NamePrefix": "DR.",
      "Credential": "MD",
      "FirstLineMailingAddress": "623 W HIGHLAND DR",
      "MailingAddressCityName": "SEATTLE",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98119-3446",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "206-282-2716",
      "FirstLinePracticeLocationAddress": "16150 NE 85TH ST STE 206",
      "SecondLinePracticeLocationAddress": "REDMOND EYE CLINIC",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3543",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-3574",
      "EnumerationDate": "05/04/2007",
      "LastUpdateDate": "07/08/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207W00000X",
      "Taxonomy1": "Ophthalmology",
      "LicenseNumber1": "MD00039796",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1659320539",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "MONTECILLO",
      "FirstName": "RANIA",
      "MiddleName": "B",
      "NamePrefix": "DR.",
      "Credential": "OD",
      "FirstLineMailingAddress": "16375 NE 85TH ST",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3554",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-7363",
      "MailingAddressFaxNumber": "425-861-5585",
      "FirstLinePracticeLocationAddress": "16375 NE 85TH ST",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052-3554",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-7363",
      "PracticeLocationAddressFaxNumber": "425-861-5585",
      "EnumerationDate": "05/09/2006",
      "LastUpdateDate": "12/19/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "LicenseNumber1": "3680",
      "LicenseNumberStateCode1": "WA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1427560267",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "ABOU SHADI",
      "FirstName": "RANIA",
      "NamePrefix": "MRS.",
      "Credential": "RPH",
      "FirstLineMailingAddress": "8862 161ST AVENUE NE",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-883-9532",
      "MailingAddressFaxNumber": "425-882-2743",
      "FirstLinePracticeLocationAddress": "8862 161ST AVENUE NE",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-883-9532",
      "PracticeLocationAddressFaxNumber": "425-882-2743",
      "EnumerationDate": "11/02/2017",
      "LastUpdateDate": "11/02/2017",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "3336C0003X",
      "Taxonomy1": "Community/Retail Pharmacy",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1528050523",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "DESCHUTES EYE CLINIC PC",
      "OtherOrgName": "THE EYE SURGERY INSTITUTE",
      "OtherOrgNameTypeCode": "3",
      "FirstLineMailingAddress": "813 SW HIGHLAND AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-3123",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-548-7170",
      "MailingAddressFaxNumber": "541-548-3842",
      "FirstLinePracticeLocationAddress": "813 SW HIGHLAND AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-3123",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-548-7170",
      "PracticeLocationAddressFaxNumber": "541-548-3842",
      "EnumerationDate": "08/17/2005",
      "LastUpdateDate": "12/01/2010",
      "AuthorizedOfficialLastName": "TRAUSTASON",
      "AuthorizedOfficialFirstName": "OLI",
      "AuthorizedOfficialMiddleName": "I",
      "AuthorizedOfficialTitle": "PRESIDENT",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "M.D.",
      "AuthorizedOfficialTelephoneNumber": "541-548-7170",
      "TaxonomyCode1": "207W00000X",
      "Taxonomy1": "Ophthalmology",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "053857000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierState1": "OR",
      "OtherIdentifierIssuer1": "REGENCE BCBS",
      "OtherIdentifier2": "CJ8770",
      "OtherIdentifierType2": "OTHER",
      "OtherIdentifierState2": "OR",
      "OtherIdentifierIssuer2": "RAILROAD MEDICARE",
      "OtherIdentifier3": "38080A",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierState3": "OR",
      "OtherIdentifierIssuer3": "CLEAR CHOICE",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization."
    },
    {
      "NPI": "1477596252",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "EYE CARE SPECIALISTS NORTHWEST PLLC",
      "OtherOrgName": "THE CHILDRENS EYE DOCTORS, THE FAMILY EYE DOCTORS, WOODLAWN OPTICAL",
      "OtherOrgNameTypeCode": "3",
      "FirstLineMailingAddress": "17130 AVONDALE WAY NE",
      "SecondLineMailingAddress": "SUITE 111",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-6600",
      "MailingAddressFaxNumber": "425-885-6580",
      "FirstLinePracticeLocationAddress": "17130 AVONDALE WAY NE",
      "SecondLinePracticeLocationAddress": "SUITE 111",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
      "PracticeLocationAddressPostalCode": "98052",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "425-885-6600",
      "PracticeLocationAddressFaxNumber": "425-885-6580",
      "EnumerationDate": "06/13/2006",
      "LastUpdateDate": "03/03/2008",
      "AuthorizedOfficialLastName": "LENART",
      "AuthorizedOfficialFirstName": "THOMAS",
      "AuthorizedOfficialTitle": "OWNER",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "MD PHD",
      "AuthorizedOfficialTelephoneNumber": "425-885-6600",
      "TaxonomyCode1": "152W00000X",
      "Taxonomy1": "Optometrist",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "156FX1800X",
      "Taxonomy2": "Optician",
      "PrimaryTaxonomySwitch2": "N",
      "TaxonomyCode3": "207W00000X",
      "Taxonomy3": "Ophthalmology",
      "PrimaryTaxonomySwitch3": "Y",
      "OtherIdentifier1": "1568514032",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "NPI",
      "OtherIdentifier2": "1740297829",
      "OtherIdentifierType2": "OTHER",
      "OtherIdentifierIssuer2": "NPI",
      "OtherIdentifier3": "1205989522",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "NPI",
      "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.",
      "HealthcareProviderTaxonomyGroup2": "193200000X MULTI-SPECIALTY GROUP",
      "HealthcareProviderTaxonomyGroupDescription2": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization.",
      "HealthcareProviderTaxonomyGroup3": "193200000X MULTI-SPECIALTY GROUP",
      "HealthcareProviderTaxonomyGroupDescription3": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization."
    },
    {
      "NPI": "1215029343",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "EYE HEALTH PROFESSIONALS, P.C.",
      "FirstLineMailingAddress": "85 BARNES RD",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "WALLINGFORD",
      "MailingAddressStateName": "CT",
      "MailingAddressPostalCode": "06492-1832",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "203-284-9448",
      "MailingAddressFaxNumber": "203-269-1361",
      "FirstLinePracticeLocationAddress": "85 BARNES RD",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "WALLINGFORD",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06492-1832",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "203-284-9448",
      "PracticeLocationAddressFaxNumber": "203-269-1361",
      "EnumerationDate": "09/28/2006",
      "LastUpdateDate": "03/07/2008",
      "AuthorizedOfficialLastName": "REDMOND",
      "AuthorizedOfficialFirstName": "JOHN",
      "AuthorizedOfficialMiddleName": "W",
      "AuthorizedOfficialTitle": "PRESIDENT",
      "AuthorizedOfficialNamePrefix": "DR.",
      "AuthorizedOfficialCredential": "M.D.",
      "AuthorizedOfficialTelephoneNumber": "203-284-9448",
      "TaxonomyCode1": "207W00000X",
      "Taxonomy1": "Ophthalmology",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization."
    },
    {
      "NPI": "1982789863",
      "EntityType": "Organization",
      "EIN": "N/A",
      "OrgName": "OVERLAKE EYE DESIGNS, P.C.",
      "FirstLineMailingAddress": "15230 NE 24TH ST STE Q",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-5540",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-562-2015",
      "MailingAddressFaxNumber": "425-562-2010",
      "FirstLinePracticeLocationAddress": "15230 NE 24TH ST STE Q",
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      "MailingAddressPostalCode": "34787-3546",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "407-905-8827",
      "MailingAddressFaxNumber": "407-645-4587",
      "FirstLinePracticeLocationAddress": "7900 FOREST CITY RD",
      "PracticeLocationAddressCityName": "ORLANDO",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "32810-3002",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "407-905-8827",
      "PracticeLocationAddressFaxNumber": "407-645-4587",
      "EnumerationDate": "02/28/2006",
      "LastUpdateDate": "07/28/2017",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "1223G0001X",
      "Taxonomy1": "General Practice",
      "LicenseNumber1": "DN15582",
      "LicenseNumberStateCode1": "FL",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "122300000X",
      "Taxonomy2": "Dentist",
      "LicenseNumber2": "DN15582",
      "LicenseNumberStateCode2": "FL",
      "PrimaryTaxonomySwitch2": "Y",
      "OtherIdentifier1": "075156100",
      "OtherIdentifierType1": "MEDICAID",
      "OtherIdentifierState1": "FL"
    },
    {
      "NPI": "1720032899",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ALBATAINEH",
      "FirstName": "RANIA",
      "MiddleName": "QASSIEM",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "11476 OKEECHOBEE BLVD",
      "MailingAddressCityName": "ROYAL PALM BEACH",
      "MailingAddressStateName": "FL",
      "MailingAddressPostalCode": "33411-8715",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "561-204-5111",
      "MailingAddressFaxNumber": "561-204-5150",
      "FirstLinePracticeLocationAddress": "11476 OKEECHOBEE BLVD",
      "PracticeLocationAddressCityName": "ROYAL PALM BEACH",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "33411-8715",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "561-204-5111",
      "PracticeLocationAddressFaxNumber": "561-204-5150",
      "EnumerationDate": "05/21/2006",
      "LastUpdateDate": "09/11/2007",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "ME 79876",
      "LicenseNumberStateCode1": "FL",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1326095100",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ROSBOROUGH",
      "FirstName": "RANIA",
      "MiddleName": "BAJWA",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "3100 WYMAN PARK DR",
      "MailingAddressCityName": "BALTIMORE",
      "MailingAddressStateName": "MD",
      "MailingAddressPostalCode": "21211-2803",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "410-338-3500",
      "FirstLinePracticeLocationAddress": "3601 SW 160TH AVE",
      "SecondLinePracticeLocationAddress": "SUITE 250",
      "PracticeLocationAddressCityName": "MIRAMAR",
      "PracticeLocationAddressStateName": "FL",
      "PracticeLocationAddressPostalCode": "33027-6308",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "877-866-7123",
      "EnumerationDate": "05/27/2006",
      "LastUpdateDate": "12/10/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "D0063732",
      "LicenseNumberStateCode1": "MD",
      "PrimaryTaxonomySwitch1": "Y",
      "TaxonomyCode2": "207Q00000X",
      "Taxonomy2": "Family Medicine",
      "LicenseNumber2": "0101257197",
      "LicenseNumberStateCode2": "VA",
      "PrimaryTaxonomySwitch2": "N"
    },
    {
      "NPI": "1528015310",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "HUSSEINI",
      "FirstName": "RANIA",
      "MiddleName": "I",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "111 CYPRESS ST",
      "MailingAddressCityName": "BROOKLINE",
      "MailingAddressStateName": "MA",
      "MailingAddressPostalCode": "02445-6002",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "508-718-4050",
      "FirstLinePracticeLocationAddress": "20 PATRIOT PL",
      "PracticeLocationAddressCityName": "FOXBORO",
      "PracticeLocationAddressStateName": "MA",
      "PracticeLocationAddressPostalCode": "02035-1375",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "508-718-4050",
      "EnumerationDate": "05/27/2006",
      "LastUpdateDate": "04/17/2012",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "209649",
      "LicenseNumberStateCode1": "MA",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1760429591",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "RAYES-DANAN",
      "FirstName": "RANIA",
      "NamePrefix": "DR.",
      "Credential": "MD",
      "OtherLastName": "RAYES",
      "OtherFirstName": "RANIA",
      "OtherLastNameTypeCode": "1",
      "FirstLineMailingAddress": "2500 METROHEALTH DR",
      "MailingAddressCityName": "CLEVELAND",
      "MailingAddressStateName": "OH",
      "MailingAddressPostalCode": "44109-1900",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "216-778-7800",
      "FirstLinePracticeLocationAddress": "2500 METROHEALTH DR",
      "PracticeLocationAddressCityName": "CLEVELAND",
      "PracticeLocationAddressStateName": "OH",
      "PracticeLocationAddressPostalCode": "44109-1900",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "216-778-7800",
      "EnumerationDate": "06/01/2006",
      "LastUpdateDate": "01/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207ZP0102X",
      "Taxonomy1": "Anatomic Pathology & Clinical Pathology",
      "LicenseNumber1": "35086346",
      "LicenseNumberStateCode1": "OH",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "2687703",
      "OtherIdentifierType1": "MEDICAID",
      "OtherIdentifierState1": "OH"
    },
    {
      "NPI": "1699717660",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "AMPEY",
      "FirstName": "RANIA",
      "MiddleName": "L",
      "Credential": "LPC",
      "FirstLineMailingAddress": "5930 LOVERS LN",
      "SecondLineMailingAddress": "PREMIER NEUROPSYCHIATRY, PLC",
      "MailingAddressCityName": "PORTAGE",
      "MailingAddressStateName": "MI",
      "MailingAddressPostalCode": "49002-1673",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "269-873-1611",
      "FirstLinePracticeLocationAddress": "5930 LOVERS LN",
      "SecondLinePracticeLocationAddress": "PREMIER NEUROPSYCHIATRY, PLC",
      "PracticeLocationAddressCityName": "PORTAGE",
      "PracticeLocationAddressStateName": "MI",
      "PracticeLocationAddressPostalCode": "49002-1673",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "269-873-1611",
      "EnumerationDate": "06/12/2006",
      "LastUpdateDate": "12/30/2010",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional",
      "LicenseNumber1": "6401007658",
      "LicenseNumberStateCode1": "MI",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1801839667",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "ABOUJAOUDE",
      "FirstName": "RANIA",
      "Credential": "M.D.",
      "FirstLineMailingAddress": "PO BOX 1283",
      "MailingAddressCityName": "MEDFORD",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08055-6283",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "609-677-1046",
      "MailingAddressFaxNumber": "609-677-1306",
      "FirstLinePracticeLocationAddress": "200 TRENTON RD",
      "PracticeLocationAddressCityName": "BROWNS MILLS",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08015-1705",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "609-677-1046",
      "PracticeLocationAddressFaxNumber": "609-677-1306",
      "EnumerationDate": "06/13/2006",
      "LastUpdateDate": "09/15/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207RI0200X",
      "Taxonomy1": "Infectious Disease",
      "LicenseNumber1": "39215",
      "LicenseNumberStateCode1": "KY",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "207RI0200X",
      "Taxonomy2": "Infectious Disease",
      "LicenseNumber2": "25MA07672000",
      "LicenseNumberStateCode2": "NJ",
      "PrimaryTaxonomySwitch2": "Y"
    },
    {
      "NPI": "1184645301",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "BAIK",
      "FirstName": "RANIA",
      "Credential": "D.O.",
      "FirstLineMailingAddress": "602 ROUTE 169",
      "SecondLineMailingAddress": "PO BOX 865",
      "MailingAddressCityName": "WOODSTOCK",
      "MailingAddressStateName": "CT",
      "MailingAddressPostalCode": "06281-2225",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "860-821-3406",
      "MailingAddressFaxNumber": "860-821-3407",
      "FirstLinePracticeLocationAddress": "602 ROUTE 169",
      "PracticeLocationAddressCityName": "WOODSTOCK",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06281-2225",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "860-821-3406",
      "PracticeLocationAddressFaxNumber": "860-821-3407",
      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

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

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

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

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

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

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

            Console.WriteLine(response);

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

                
{
  "NPI": [
    {
      "NPI": "1083349906",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "STAFFORD",
      "FirstName": "KADY",
      "NamePrefix": "MS.",
      "Credential": "LPC",
      "FirstLineMailingAddress": "13574 SW HIGHWAY 126",
      "MailingAddressCityName": "POWELL BUTTE",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97753-1541",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-480-6360",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-203-0307",
      "EnumerationDate": "07/24/2022",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional Counselor",
      "LicenseNumber1": "LPC6225",
      "LicenseNumberStateCode1": "ID",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C9084",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1215724679",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "SCHAY",
      "FirstName": "ANGELICA",
      "MiddleName": "NICOLE",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1841",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
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}
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