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    NDC 43742-2095-01 Pollutox 12; 12; 12; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 6; 12; 12; 15 [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_C]/mL Details

    Pollutox 12; 12; 12; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 6; 12; 12; 15 [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_C]/mL

    Pollutox is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ACETONE; ARSENIC TRIOXIDE; BENZENE; BERBERIS VULGARIS ROOT BARK; CADMIUM SULFIDE; CARBON DIOXIDE; CHLORINE; HYDROFLUORIC ACID; KEROSENE; LEAD; MELATONIN; MERCURIUS SOLUBILIS; NITROUS OXIDE; OZONE; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; TIN; TOLUENE; UR.

    Product Information

    NDC 43742-2095
    Product ID 43742-2095_58a6d6f8-caed-48e7-8217-5c148b86ef35
    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 Pollutox
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sulphuricum Acidum, Berberis Vulgaris, Arsenicum Album, Benzinum, Cadmium Sulphuratum, Hydrofluoricum Acidum, Melatonin, Nitrogenum Oxygenatum, Nux Vomica, Petroleum, Plumbum Metallicum, Stannum Metallicum, Toluene, Acetone, Carbon Dioxide, Chlorinum, Mer
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 12; 12; 12; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 6; 12; 12; 15
    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_C]/mL
    Substance Name ACETONE; ARSENIC TRIOXIDE; BENZENE; BERBERIS VULGARIS ROOT BARK; CADMIUM SULFIDE; CARBON DIOXIDE; CHLORINE; HYDROFLUORIC ACID; KEROSENE; LEAD; MELATONIN; MERCURIUS SOLUBILIS; NITROUS OXIDE; OZONE; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; TIN; TOLUENE; UR
    Labeler Name Deseret Biologicals, Inc.
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Radiographic Contrast Agent [EPC], Seed Storage Proteins [CS], X-Ray Contra
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 43742-2095-01 (43742209501)

    NDC Package Code 43742-2095-1
    Billing NDC 43742209501
    Package 30 mL in 1 BOTTLE, DROPPER (43742-2095-1)
    Marketing Start Date 2023-10-13
    NDC Exclude Flag N
    Pricing Information N/A