Label: GZE MULTI-EFFECT WHITENING SUNSCREEN- titanium dioxide,zinc oxide cream

  • NDC Code(s): 83566-122-01
  • Packager: Guangzhou Yilong Cosmetics Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 7, 2024

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  • Active ingredients

    Cannabis Sativa Leaf Extract 15.36%

    Ascorbic Acid 10%

    Titanium Dioxide 10%

    Zinc Oxide 10%

    Niacinamide 2%

  • Purpose

    For sunscreen use.

  • Uses

    Apply liberally 15 minutes before sun exposure.

  • WARNINGS

    For external use only.

  • Stop use and ask a doctor if

    rash occurs.

  • Do not use

    Do not use on damaged or broken.

  • When using this product

    When using this product, keep out of eyes. Rinse with water to remove.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Squeeze out an appropriate amount of sunscreen and spread evenly on skin.

  • INACTIVE INGREDIENT

    NIACINAMIDE
    GLYCERIN
    WATER O-15
    PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
    TREHALOSE
    ALLANTOIN

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    GZE MULTI-EFFECT WHITENING SUNSCREEN 
    titanium dioxide,zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID10 mg  in 1 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE10 mg  in 1 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE10 mg  in 1 g
    CANNABIS SATIVA LEAF (UNII: A718Z7DA1K) (CANNABIS SATIVA LEAF - UNII:A718Z7DA1K) CANNABIS SATIVA LEAF15.36 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER O-15 (UNII: 63M8RYN44N)  
    PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)  
    TREHALOSE (UNII: B8WCK70T7I)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-122-0160 g in 1 BOTTLE; Type 0: Not a Combination Product12/20/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/20/2023
    Labeler - Guangzhou Yilong Cosmetics Co.,Ltd. (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co.,Ltd.712647107manufacture(83566-122)
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