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    NDC 11523-7189-01 Bain de Soleil 25 mg/g Details

    Bain de Soleil 25 mg/g

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

    Product Information

    NDC 11523-7189
    Product ID 11523-7189_eafff815-4099-d1c7-e053-2a95a90a3375
    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 Orange Gelee SPF 4
    Non-Proprietary Name Octinoxate
    Product Type HUMAN OTC DRUG
    Dosage Form GEL
    Route TOPICAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/g
    Substance Name OCTINOXATE
    Labeler Name Bayer HealthCare LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part352
    Listing Certified Through 2023-12-31

    Package

    NDC 11523-7189-01 (11523718901)

    NDC Package Code 11523-7189-1
    Billing NDC 11523718901
    Package 1 TUBE in 1 CARTON (11523-7189-1) / 88 g in 1 TUBE
    Marketing Start Date 1999-05-21
    NDC Exclude Flag N
    Pricing Information N/A
    << 11523-7162-03 11523-7200-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 7222f6f9-689e-4e00-91f5-4db159348dfd Details

    Revised: 10/2022
    Document Id: eafff815-4099-d1c7-e053-2a95a90a3375
    Set id: 7222f6f9-689e-4e00-91f5-4db159348dfd
    Version: 5
    Effective Time: 20221014