Search by Drug Name or NDC

    NDC 50390-0001-30 Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium 20; 55; 5; 8.8; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL Details

    Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium 20; 55; 5; 8.8; 98 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL

    Artistry Ideal Radiance Illuminating CC SPF 50 Broad Spectrum Sunscreen Light/Medium is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Amway Corp. The primary component is ENSULIZOLE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE.

    Product Information

    NDC 50390-0001
    Product ID 50390-001_08370288-7313-b684-e063-6294a90ad541
    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 SPF 50 Broad Spectrum Sunscreen Light/Medium
    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 Amway Corp
    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 50390-0001-30 (50390000130)

    NDC Package Code 50390-001-30
    Billing NDC 50390000130
    Package 1 TUBE in 1 CARTON (50390-001-30) / 30 mL in 1 TUBE
    Marketing Start Date 2015-05-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 50383-0979-04 50390-0002-30 >>

    Contents