Label: DRUGGIST KOJIC ACID DARK SPOT REMOVER capsule

  • NDC Code(s): 83872-140-01
  • Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 12, 2024

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  • ACTIVE INGREDIENT


    Curcuma Longa (Turmeric) Root Powder: 5%
    Hyaluronic Acid: 3%
    Retinol: 3%
    Collagen: 3%
    Kojic Acid: 7%

  • PURPOSE

    Moisturizing, whitening, reducing wrinkles and fine lines, reducing pigmentation, improving skin's luster and elasticity.

  • Uses

    Pigmentation

  • 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 contact Poison Control Center right away

  • Directions for use

    Latherinto wet skin and rinse off immediately.Safe for body and face use.

  • INACTIVE INGREDIENT

    Stearic Acid: 15%
    Lauric Acid: 9%
    Glycerin: 18%
    Sodium Hydroxide: 0.5%
    Sodium Laureth Sulfate: 6%
    Disodium EDTA: 0.7%
    Sucrose Laurate: 2%
    BHT: 0.6%
    Propylene Glycol Dioleate: 3.1%
    Decyl Glucoside: 7%
    Shea Butter Oleyl Esters: 4%
    PPG-25 Sorbitol: 2%
    Olive Oil: 3%
    PEG-10 Esters: 2%
    HC Yellow No.5: 0.1%
    Ascorbic Acid : 3%
    Tocopherol : 3%

  • Other Information

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

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DRUGGIST KOJIC ACID DARK SPOT REMOVER 
    druggist kojic acid dark spot remover capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-140
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID30 mg  in 1 g
    RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL30 mg  in 1 g
    KOJIC ACID (UNII: 6K23F1TT52) (KOJIC ACID - UNII:6K23F1TT52) KOJIC ACID70 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0) 60 mg  in 1 g
    GLYCERIN (UNII: PDC6A3C0OX) 180 mg  in 1 g
    PROPYLENE GLYCOL DIOLEATE (UNII: 84T0LSN7U6) 31 mg  in 1 g
    OLIVE OIL (UNII: 6UYK2W1W1E) 30 mg  in 1 g
    SUCROSE LAURATE (UNII: 05Q7CD0E49) 20 mg  in 1 g
    SODIUM HYDROXIDE (UNII: 55X04QC32I) 5 mg  in 1 g
    HC YELLOW NO. 5 (UNII: I844A312T7) 1 mg  in 1 g
    STEARIC ACID (UNII: 4ELV7Z65AP) 150 mg  in 1 g
    LAURIC ACID (UNII: 1160N9NU9U) 90 mg  in 1 g
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) 6 mg  in 1 g
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y) 70 mg  in 1 g
    ASCORBIC ACID (UNII: PQ6CK8PD0R) 30 mg  in 1 g
    TOCOPHEROL (UNII: R0ZB2556P8) 30 mg  in 1 g
    Product Characteristics
    ColororangeScoreno score
    ShapeRECTANGLESize75mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-140-01135 g in 1 BOTTLE; Type 0: Not a Combination Product05/13/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01605/13/2024
    Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen XiaoMai Manufacturing Co., Ltd.712999147manufacture(83872-140)
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