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    NDC 61924-0102-34 HAND-E-FOAM 0.002 g/mL Details

    HAND-E-FOAM 0.002 g/mL

    HAND-E-FOAM is a TOPICAL AEROSOL, FOAM in the HUMAN OTC DRUG category. It is labeled and distributed by DermaRite Industries, LLC. The primary component is BENZETHONIUM CHLORIDE.

    Product Information

    NDC 61924-0102
    Product ID 61924-102_d58c97e0-1af0-fe52-e053-2a95a90a5649
    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 HAND-E-FOAM
    Proprietary Name Suffix n/a
    Non-Proprietary Name OTC ANTIMICROBIAL DRUG PRODUCTS
    Product Type HUMAN OTC DRUG
    Dosage Form AEROSOL, FOAM
    Route TOPICAL
    Active Ingredient Strength 0.002
    Active Ingredient Units g/mL
    Substance Name BENZETHONIUM CHLORIDE
    Labeler Name DermaRite Industries, LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part333A
    Listing Certified Through 2023-12-31

    Package

    NDC 61924-0102-34 (61924010234)

    NDC Package Code 61924-102-34
    Billing NDC 61924010234
    Package 1000 mL in 1 CARTRIDGE (61924-102-34)
    Marketing Start Date 2002-08-08
    NDC Exclude Flag N
    Pricing Information N/A
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