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    NDC 10056-0030-30 Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light 20; 55; 5; 8.8; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

    Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light 20; 55; 5; 8.8; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

    Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Access Business Group LLC. The primary component is ENSULIZOLE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE.

    Product Information

    NDC 10056-0030
    Product ID 10056-030_083752d6-b759-692f-e063-6294a90aa338
    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 Artistry Ideal Radiance Illuminating CC SPF50 Broad Spectrum Sunscreen - Light
    Proprietary Name Suffix n/a
    Non-Proprietary Name ENSULIZOLE,OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE
    Product Type HUMAN OTC DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 20; 55; 5; 8.8; 98
    Active Ingredient Units mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
    Substance Name ENSULIZOLE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
    Labeler Name Access Business Group LLC
    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 2024-12-31

    Package

    NDC 10056-0030-30 (10056003030)

    NDC Package Code 10056-030-30
    Billing NDC 10056003030
    Package 1 BOTTLE, PLASTIC in 1 CARTON (10056-030-30) / 30 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2015-12-11
    NDC Exclude Flag N
    Pricing Information N/A