Label: DARKSPOTREMOVERILLUMINATINGFACECREAM emulsion

  • NDC Code(s): 84423-046-01
  • Packager: Guangzhou Kadiya Biotechnology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 17, 2024

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  • PURPOSE

    For skin whitening, moisturising and dark spots

  • INACTIVE INGREDIENT

    AQUA,PROPYLENE GLYCOL,GLYCERIN,MINERAL OIL,PALMITIC ACID,DIMETHICONE,POLYSORBATE 60,GLYCERYL STEARATE,STEARYL ALCOHOL,TRANEXAMIC ACID,TITANIUM DIOXIDE,CETYL ALCOHOL,PEG-50 LANOLIN,TRIETHANOLAMINE,PEG-75 LANOLIN,PHENOXYETHANOL,HYDROGENATED LECITHIN,ALLANTOIN,STEARIC ACID,LANOLIN,METHYLPARABEN,MYRISTIC ACID,PROPYLPARABEN,ALUMINA,YEAST FERMENT EXTRACT

  • WARNINGS

    1、For external use only, avoid contact with eyes when used
    2、Keep out of reach of children

  • INDICATIONS & USAGE

    Thie s mdieturizina croam onrichod fem avouieito and powertul ingredients that also removes dark spots (from acne. hvper pigmentation, etc). It contains vitamins C & E and provides a SPF of 15. This product will nourish and refine skin. linhten dark snots and smooth nores This product has been formulated for sensitive skin.

  • DOSAGE & ADMINISTRATION

    Apply to Hyperpigmented area 2-3 times daily to even out face and neck tone. Avoid contact with eyes. Results will continue to improve with daily use.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN SECTION

  • ACTIVE INGREDIENT

    ALPHA-ARBUTIN1%
    HYDROLYZED COLLAGEN EXTRACT0.5%
    TOCOPHEROL0.5%
    ASCORBIC ACID0.1%

  • PRINCIPAL DISPLAY PANEL

    Active Ingredients
    ALPHA-ARBUTIN 1%
    HYDROLYZED COLLAGEN EXTRACT 0.5%
    TOCOPHEROL 0.5%
    ASCORBIC ACID 0.1%


    Uses:
    For skin whitening, moisturising and dark spots


    The storage method:
    Store sealed in a cool place and out of sunlight

    Warning.
    1、For external use only, avoid contact with eyes when used
    2、Keep out of reach of children

    Inactive ingredients:
    AQUA,PROPYLENE GLYCOL,GLYCERIN,MINERAL OIL,PALMITIC ACID,DIMETHICONE,POLYSORBATE 60,GLYCERYL STEARATE,STEARYL ALCOHOL,TRANEXAMIC ACID,TITANIUM DIOXIDE,CETYL ALCOHOL,PEG-50 LANOLIN,TRIETHANOLAMINE,PEG-75 LANOLIN,PHENOXYETHANOL,HYDROGENATED LECITHIN,ALLANTOIN,STEARIC ACID,LANOLIN,METHYLPARABEN,MYRISTIC ACID,PROPYLPARABEN,ALUMINA,YEAST FERMENT EXTRACT

    GM LABEL

  • INGREDIENTS AND APPEARANCE
    DARKSPOTREMOVERILLUMINATINGFACECREAM 
    darkspotremoverilluminatingfacecream emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84423-046
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN0.3 g  in 30 mL
    TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL0.015 g  in 30 mL
    ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID0.03 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TRANEXAMIC ACID (UNII: 6T84R30KC1)  
    PEG-50 LANOLIN (UNII: 2U8P432R6Z)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    AQUA (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ALUMINA (UNII: LMI26O6933)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    GLYCERYL STEARATE (UNII: 230OU9XXE4)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84423-046-0130 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product12/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01612/17/2024
    Labeler - Guangzhou Kadiya Biotechnology Co., Ltd. (713172913)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Kadiya Biotechnology Co., Ltd.713172913manufacture(84423-046)