Label: GZE AHA BODYLOTION- arbutin 0.4% glutathione 0.1% niacinamide 0.1% cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2024

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  • ACTIVE INGREDIENT

    Arbutin 0.4%
    Glutathione 0.1%
    Niacinamide 0.1%

  • INACTIVE INGREDIENT

    Water

    Cyclopentasiloxane

    Dimethicone

    Glycerin

    Diethylhexyl Carbonate

    Titanium Dioxide

    Butylene Glycol

    C12-15 Alkyl Benzoate

    Polymethylsilsesquioxane

    Citric acid

    Polyglyceryl-4Diisostearate/

    Polyhydroxystearate/Sebacate

    Ethylhexyl Methoxycinnamate

    Cetyl PEG/PPG-10/1 Dimethicone

    Imidazolidinyl Urea

    Benzophenone-3

    Cetearyl Dimethicone Crosspolymer

    Sodium Chloride

    Hydrolyzed Extensin

    Phospholipids

    Parfum

    Phenoxyethanol

    Betaine

    Collagen

  • INDICATIONS & USAGE


    Apply over your body daily
    in the morning andbefore bed.

  • DOSAGE & ADMINISTRATION


    Apply over your body daily in the morning and before bed.

  • PURPOSE

    Moisturizing

  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • DO NOT USE

  • WHEN USING

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • PRINCIPAL DISPLAY PANEL

    product image

  • INGREDIENTS AND APPEARANCE
    GZE AHA BODYLOTION 
    arbutin 0.4% glutathione 0.1% niacinamide 0.1% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74458-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN0.4 g  in 100 g
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.1 g  in 100 g
    GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZOPHENONE-3 (UNII: 95OOS7VE0Y)  
    CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)  
    EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ETHYLHEXYL METHOXYCINNAMATE (UNII: 4Y5P7MUD51)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    POLYMETHYLSILSESQUIOXANE (UNII: 59Z907ZB69)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    BETAINE (UNII: 3SCV180C9W)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)  
    IMIDAZOLIDINYL UREA (UNII: M629807ATL)  
    HUMAN TYPE I COLLAGEN (UNII: PT3TGI7OIP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74458-020-0140 g in 1 TUBE; Type 0: Not a Combination Product11/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/09/2024
    Labeler - Guangzhou Yilong Cosmetics Co., Ltd (420929116)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co., Ltd420929116manufacture(74458-020)
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