Label: FADING CREAM SNOW BLEACH FOR BODY cream

  • NDC Code(s): 83872-123-01
  • Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 2, 2024

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  • ACTIVE INGREDIENT

    Glycolic Acid: 3.0%
    Kojic Acid: 2.0%
    Arbutin: 2.0%
    Hydroquinone: 1.0%

  • PURPOSE

    Suitable for body whitening,making the skin more even and radiant.

  • Uses

    Used to reduce skin,pigmentation and fading

  • WARNINGS

    For external use only. Avoid contact with eyes and mucous membranes.

  • Do not use


    on damaged or broken skin.

  • When using this product

    For external use only. Avoid contact with eyes and mucous membranes.

  • Stop use and ask a doctor

    Discontinue use ifirritation occurs,

  • Keep out of reach of children.

    Keep out of reach of children.

  • Directions for use

    1.Apply the product evenly onto clean skin.
    2.Massage until fully absorbed.
    3.Use daly for several weeks for best results.

  • INACTIVE INGREDIENT

    Aqua (Water): 70.0%
    Glycerin: 5.0%
    Cetearyl Alcohol: 3.0%
    Stearic Acid: 3.0%
    Caprylic/Capric Triglyceride: 10.0%
    Phenoxyethanol: 1.0%

  • Other Information

    Store in a cool, dry place away from direct sunlight and heat.
    Keep packaging intact.

  • PRINCIPAL DISPLAY PANEL

    6

  • INGREDIENTS AND APPEARANCE
    FADING CREAM SNOW BLEACH FOR BODY 
    fading cream snow bleach for body cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-123
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID20 mg  in 1 g
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN20 mg  in 1 g
    GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S) GLYCOLIC ACID30 mg  in 1 g
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 700 mg  in 1 g
    GLYCERIN (UNII: PDC6A3C0OX) 50 mg  in 1 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 30 mg  in 1 g
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 10 mg  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-123-0150 g in 1 BOTTLE; Type 0: Not a Combination Product05/02/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/02/2024
    Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen XiaoMai Manufacturing Co., Ltd.712999147manufacture(83872-123)
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