Label: DARK SPOT CORRECTOR CREAM cream

  • NDC Code(s): 83872-122-01
  • 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

    Collagen: 5.0%
    Active Pigment Concentrate: 2.0%
    Glycerin: 5.0%

  • PURPOSE

    Used to reduce dark spots and pigmentation.

  • Uses

    Dark spots and pigmentation.

  • WARNINGS

    For external use only. Avoid contact with eyes.

  • Do not use


    on damaged or broken skin.

  • When using this product

    keep out of eyes.
    Rinse with water to remove.

  • Stop use and ask a doctor

    Discontinue use if irritation occurs.

  • Keep out of reach of children.

    Keep out of reach of children.

  • Directions for use

    1. Apply the product to clean face and neck.
    2.Gently massage until fully absorbed.
    3.Use twice daily as part of your daily skincare routine.

  • INACTIVE INGREDIENT

    Aqua (Water): 70.0%
    Cetearyl Alcohol: 3.0%
    Stearic Acid: 3.0%
    Caprylic/Capric Triglyceride: 10.0%
    Phenoxyethanol: 2.0%

  • STORAGE AND HANDLING

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

  • PRINCIPAL DISPLAY PANEL

    5

  • INGREDIENTS AND APPEARANCE
    DARK SPOT CORRECTOR CREAM 
    dark spot corrector cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 700 mg  in 1 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 30 mg  in 1 g
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 20 mg  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-122-0150 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(83872-122)
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