Search by Drug Name or NDC

    NDC 61296-0017-00 BIOSOLIS Face Sunscreen Broadspectrum SPF50 100; 152 mg/mL; mg/mL Details

    BIOSOLIS Face Sunscreen Broadspectrum SPF50 100; 152 mg/mL; mg/mL

    BIOSOLIS Face Sunscreen Broadspectrum SPF50 is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Pro Vera SA. The primary component is TITANIUM DIOXIDE; ZINC OXIDE.

    Product Information

    NDC 61296-0017
    Product ID 61296-017_0e99626b-7593-3342-e063-6394a90a4498
    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 BIOSOLIS Face Sunscreen Broadspectrum SPF50
    Proprietary Name Suffix n/a
    Non-Proprietary Name TITANIUM DIOXIDE, ZINC OXIDE
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 100; 152
    Active Ingredient Units mg/mL; mg/mL
    Substance Name TITANIUM DIOXIDE; ZINC OXIDE
    Labeler Name Pro Vera SA
    Pharmaceutical Class Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M020
    Listing Certified Through n/a

    Package

    NDC 61296-0017-00 (61296001700)

    NDC Package Code 61296-017-00
    Billing NDC 61296001700
    Package 1 BOTTLE, PUMP in 1 BOX (61296-017-00) / 50 mL in 1 BOTTLE, PUMP
    Marketing Start Date 2022-01-07
    NDC Exclude Flag N
    Pricing Information N/A
    << 61296-0016-00 61296-0018-00 >>

    Contents