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    NDC 00135-0568-04 SENSODYNE PRONAMEL 50; 1.15 mg/g; mg/g Details

    SENSODYNE PRONAMEL 50; 1.15 mg/g; mg/g

    SENSODYNE PRONAMEL is a ORAL PASTE in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is POTASSIUM NITRATE; SODIUM FLUORIDE.

    Product Information

    NDC 00135-0568
    Product ID 0135-0568_09413dec-15c0-0ec8-e063-6294a90a191c
    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 SENSODYNE PRONAMEL
    Proprietary Name Suffix Multi Action
    Non-Proprietary Name potassium nitrate and sodium fluoride
    Product Type HUMAN OTC DRUG
    Dosage Form PASTE
    Route ORAL
    Active Ingredient Strength 50; 1.15
    Active Ingredient Units mg/g; mg/g
    Substance Name POTASSIUM NITRATE; SODIUM FLUORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M022
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0568-04 (00135056804)

    NDC Package Code 0135-0568-04
    Billing NDC 00135056804
    Package 1 TUBE in 1 CARTON (0135-0568-04) / 113 g in 1 TUBE
    Marketing Start Date 2013-12-09
    NDC Exclude Flag N
    Pricing Information N/A
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