Label: KOJIC ACID DARK SPOT- soap soap

  • NDC Code(s): 83872-416-01
  • Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 9, 2024

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  • Active ingredients

    Kojic Acid 20%

  • Purpose

    Anti-wrinkle, moisturizes

  • Uses

    Anti-wrinkle, moisturizes, nourishes and repairs skin, keeping skin hydrated, soft and smooth.

  • Warnings

    For external use only
    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 if rash occurs
    Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

  • Do not use

    Do not use on damaged or broken skin

  • When using this product

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

  • Stop use and ask a doctor if

    Stop use and ask a doctor if rash occurs

  • Keep out of reach of children.

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

  • Ask Doctor

    When Pregnant or breast-feeding.

  • Directions

    1. After cleansing the face, take an appropriate amount of spot lightening cream.
    2. Apply evenly to the area on the face that needs to lighten spots, and massage gently until completely absorbed.
    3. Use once in the morning and evening. Continuous use will provide better results.

  • Other information

    Please store in a cool, dry place away from direct sunlight.

  • Inactive ingredients

    Alkyl Polyglucoside (APG), Glycerin, Decyl Glucoside, Ascorbic Acid (Vitamin C)Retinol, Kojic Acid. Collagen, Hyaluronic Acid, Turmeric P.E, Sodium Chloride, Aqua, SheaButter, Vitamin E, Olive Oil, Fragrance, FD&C Yellow, FD&C Red.

  • PRINCIPAL DISPLAY PANEL

    LBEALLBEAL

  • INGREDIENTS AND APPEARANCE
    KOJIC ACID DARK SPOT 
    soap soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-416
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID50 g  in 420 g
    Inactive Ingredients
    Ingredient NameStrength
    RETINOL (UNII: G2SH0XKK91)  
    FD&C RED NO. 3 (UNII: PN2ZH5LOQY)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    TURMERIC (UNII: 856YO1Z64F)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-416-01420 g in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product08/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/10/2024
    Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xiaomai Manufacturing Co., Ltd.712999147manufacture(83872-416)
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