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    NDC 70186-0612-01 LIGHT WONDER YOUR LIGHT, DREAM SKIN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 1.76; 1 g/40mL; g/40mL Details

    LIGHT WONDER YOUR LIGHT, DREAM SKIN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 1.76; 1 g/40mL; g/40mL

    LIGHT WONDER YOUR LIGHT, DREAM SKIN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15 is a TOPICAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by Charlotte Tilbury Beauty Ltd.. The primary component is OCTINOXATE; TITANIUM DIOXIDE.

    Product Information

    NDC 70186-0612
    Product ID 70186-612_822be17d-994f-45a1-b89b-e42459b6422f
    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 LIGHT WONDER YOUR LIGHT, DREAM SKIN FOUNDATION SUNSCREEN BROAD SPECTRUM SPF 15
    Proprietary Name Suffix n/a
    Non-Proprietary Name Octinoxate and Titanium Dioxide
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route TOPICAL
    Active Ingredient Strength 1.76; 1
    Active Ingredient Units g/40mL; g/40mL
    Substance Name OCTINOXATE; TITANIUM DIOXIDE
    Labeler Name Charlotte Tilbury Beauty Ltd.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part352
    Listing Certified Through 2024-12-31

    Package

    NDC 70186-0612-01 (70186061201)

    NDC Package Code 70186-612-01
    Billing NDC 70186061201
    Package 1 TUBE in 1 CARTON (70186-612-01) / 40 mL in 1 TUBE
    Marketing Start Date 2019-06-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 69a3cd67-6be6-456e-9eff-4a83df1e7c4f Details

    Revised: 9/2019