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    NDC 73092-0001-01 Oxyhives 200; 6; 6; 30; 200; 6; 200; 200 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL Details

    Oxyhives 200; 6; 6; 30; 200; 6; 200; 200 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL

    Oxyhives is a ORAL SPRAY in the HUMAN OTC DRUG category. It is labeled and distributed by Publisher Payments, LLC. The primary component is APIS MELLIFERA; ARNICA MONTANA; ICHTHAMMOL; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PORK LIVER; TOXICODENDRON PUBESCENS LEAF; URTICA URENS.

    Product Information

    NDC 73092-0001
    Product ID 73092-0001_dd9732be-a0c3-4d1c-92a7-2da0ace6c098
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Oxyhives
    Proprietary Name Suffix n/a
    Non-Proprietary Name Apis Mellifica, Arnica Montana, Hepar Suis, Ichthyolum, Lachesis Mutus, Mercurius Solubilis, Rhus Tox, Urtica Urens
    Product Type HUMAN OTC DRUG
    Dosage Form SPRAY
    Route ORAL
    Active Ingredient Strength 200; 6; 6; 30; 200; 6; 200; 200
    Active Ingredient Units [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL
    Substance Name APIS MELLIFERA; ARNICA MONTANA; ICHTHAMMOL; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PORK LIVER; TOXICODENDRON PUBESCENS LEAF; URTICA URENS
    Labeler Name Publisher Payments, LLC
    Pharmaceutical Class Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2023-12-31

    Package

    NDC 73092-0001-01 (73092000101)

    NDC Package Code 73092-0001-1
    Billing NDC 73092000101
    Package 30 mL in 1 BOTTLE, DROPPER (73092-0001-1)
    Marketing Start Date 2019-05-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL fef25581-524a-4766-8a0b-13aa1d648b05 Details

    Revised: 5/2019