Label: GZE BRIGHTENNG EXFOLIATING GEL- allantoin 0.5% niacinamide 5% gel

  • NDC Code(s): 74458-037-01
  • Packager: Guangzhou Yilong Cosmetics Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 20, 2024

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  • ACTIVE INGREDIENT

    Allantoin

    Niacinamide

  • INACTIVE INGREDIENT

    Aqua

    Butylene Glycol

    Glycerin

    Carbomer

    Trehalose

    Hydrolyzed Collagen

    Aloe Barbadensis Leaf Extract

    Hamamelis Virginiana (Witch Hazel) Extract

    Centella Asiatica Extract

    Phenoxyethanol

    Ethylhexylglycerin

    PEG-40 Hydrogenated Castor Oil

    Fragrance

  • INDICATIONS & USAGE


    After cleansing face, take appropriateproducts
    smear on the face. Along the skin texture and gently massagein circular
    motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

  • PURPOSE

    Exfoliating.

  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • DO NOT USE

    Do not use on damaged or broken skin.

  • WHEN USING

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION


    After cleansing face, take appropriateproducts
    smear on the face. Along the skin texture and gently massagein circular
    motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

  • PRINCIPAL DISPLAY PANEL

    product image

  • INGREDIENTS AND APPEARANCE
    GZE BRIGHTENNG EXFOLIATING GEL 
    allantoin 0.5% niacinamide 5% gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74458-037
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.5 g  in 100 g
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    HUMAN TYPE I COLLAGEN (UNII: PT3TGI7OIP)  
    ALOE BARBADENSIS LEAF EXTRACT (UNII: ZY81Z83H0X)  
    HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT (UNII: T07U1161SV)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TREHALOSE (UNII: B8WCK70T7I)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    AQUA (UNII: 059QF0KO0R)  
    CARBOMER (UNII: 0A5MM307FC)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74458-037-0150 g in 1 TUBE; Type 0: Not a Combination Product11/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01611/03/2024
    Labeler - Guangzhou Yilong Cosmetics Co., Ltd (420929116)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Yilong Cosmetics Co., Ltd420929116manufacture(74458-037)
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