Search by Drug Name or NDC

    NDC 11523-7094-01 Bain de Soleil 35; 10 mg/mL; mg/mL Details

    Bain de Soleil 35; 10 mg/mL; mg/mL

    Bain de Soleil is a TOPICAL LOTION in the HUMAN OTC DRUG category. It is labeled and distributed by Bayer HealthCare LLC.. The primary component is OCTINOXATE; OCTOCRYLENE.

    Product Information

    NDC 11523-7094
    Product ID 11523-7094_04db8d76-be3f-7134-e063-6294a90ad966
    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 Bain de Soleil
    Proprietary Name Suffix Mega Tan SPF 4
    Non-Proprietary Name Octinoxate and Octocrylene
    Product Type HUMAN OTC DRUG
    Dosage Form LOTION
    Route TOPICAL
    Active Ingredient Strength 35; 10
    Active Ingredient Units mg/mL; mg/mL
    Substance Name OCTINOXATE; OCTOCRYLENE
    Labeler Name Bayer HealthCare LLC.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part352
    Listing Certified Through 2024-12-31

    Package

    NDC 11523-7094-01 (11523709401)

    NDC Package Code 11523-7094-1
    Billing NDC 11523709401
    Package 1 TUBE in 1 CARTON (11523-7094-1) / 118 mL in 1 TUBE
    Marketing Start Date 1999-05-21
    NDC Exclude Flag N
    Pricing Information N/A
    << 11523-7020-01 11523-7157-02 >>

    Contents