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    NDC 00135-0602-02 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 00135-0602
    Product ID 0135-0602_52cc971b-ced0-403f-bac5-95a4961ca02d
    Associated GPIs 97503000004400
    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 Strong and Bright Enamel Mint
    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 NOT FINAL
    Application Number part356
    Listing Certified Through 2024-12-31

    Package

    NDC 00135-0602-02 (00135060202)

    NDC Package Code 0135-0602-02
    Billing NDC 00135060202
    Package 1 TUBE in 1 CARTON (0135-0602-02) / 23 g in 1 TUBE
    Marketing Start Date 2016-12-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL be1ae382-0e01-4db8-90d7-fdadec2ff861 Details

    Revised: 12/2020