Label: DRUGGIST PRO DARK SPOT CORRWXTOR- pro dark spot corrwxtor cream

  • NDC Code(s): 83872-200-01
  • Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 5, 2024

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  • Active ingredients


    Niacinamide3%
    Arbutin7%
    Niacinamide3%
    4-Butylresorcinol

  • Purpose

    Lighten skin spots, even skin tone, and make skin brighter.

  • Uses

    Lighten skin spots, even skin tone, and make skin brighter.

  • Wamings

    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

    Stop use and ask a doctor if rash occurs

  • When using this product

    For external use only

    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.

  • 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

    Aqua,Methylpropanediol,Butylene Glycol Stearate, Caprylic/Capric /Stearic Triglyceride,Tocopherol,Saccharomyces Polypeptides, BHT,Methylparaben, Propylparaben,Sodium Hyaluronate,Sodium Polyacrylate Starch,Trideceth-6,C18-21 Alkane.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DRUGGIST PRO DARK SPOT CORRWXTOR 
    pro dark spot corrwxtor cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    4-BUTYLRESORCINOL (UNII: 2IK4UQ3ZGA) (4-BUTYLRESORCINOL - UNII:2IK4UQ3ZGA) 4-BUTYLRESORCINOL5 g  in 100 mL
    TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL3 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE3 g  in 100 mL
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN7 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    C18-C21 ALKANE (UNII: 33822S0M40)  
    WATER (UNII: 059QF0KO0R)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-200-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01603/03/2024
    Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xiaomai Manufacturing Co., Ltd.712999147manufacture(83872-200)
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