Search by Drug Name or NDC

    NDC 43742-2089-01 Control 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

    Control 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

    Control is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ASARUM CANADENSE ROOT; BLATTA ORIENTALIS; BUFO BUFO CUTANEOUS GLAND; CLEMATIS RECTA FLOWERING TOP; CUPRIC ACETATE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; SODIUM CHLORIDE; SODIUM .

    Product Information

    NDC 43742-2089
    Product ID 43742-2089_6bac1cc6-55be-4c8e-afe8-407c8675d08a
    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 Control
    Proprietary Name Suffix n/a
    Non-Proprietary Name Anacardium Orientale, Aqua Marina, Argentum Nitricum, Asarum Canadense, Blatta Orientalis, Bufo Rana, Cerebrum Suis, Clematis Erecta, Cuprum Aceticum, Hypothalamus Suis, Ignatia Amara, Kali Phosphoricum, Lachesis Mutus, Mercurius Solubilis, Natrum Sulphur
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6
    Active Ingredient Units [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name ASARUM CANADENSE ROOT; BLATTA ORIENTALIS; BUFO BUFO CUTANEOUS GLAND; CLEMATIS RECTA FLOWERING TOP; CUPRIC ACETATE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; SODIUM CHLORIDE; SODIUM
    Labeler Name Deseret Biologicals, Inc.
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 43742-2089-01 (43742208901)

    NDC Package Code 43742-2089-1
    Billing NDC 43742208901
    Package 30 mL in 1 BOTTLE, DROPPER (43742-2089-1)
    Marketing Start Date 2023-08-23
    NDC Exclude Flag N
    Pricing Information N/A
    << 43742-2088-01 43742-2090-01 >>

    Contents