Label: 7 DAYS WHITENING FACE CREAM cream

  • NDC Code(s): 84423-006-01
  • Packager: Guangzhou Kadiya Biotechnology Co.,,Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 28, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGEDIENT

    GLUTATHIONE 0.5%
    ALPHA-ARBUTIN 1%
    ALOE BARBADENSIS1.25%

  • PURPOSE

    For Face Whitening and Hydrating

  • INACTIVE INGREDIENT

    AQUA, GLYCERIN, MINERAL OIL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL,BUTYLENE GLYCOL, PALMITIC ACID, STEARIC ACID, MYRISTIC ACID, LAURIC ACID, DIMETHICONE, NIACINAMIDE, GLYCERYL STEARATE, POLYSORBATE 60, Water, BUTYLENE GLYCOL, ANTHEMIS NOBILIS FLOWER EXTRACT, PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT, PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, TRANEXAMIC ACID, TITANIUM DIOXIDE, ALUMINA, TRIETHANOLAMINE, PEG-75 LANOLIN, PHENOXYETHANOL, ALLANTOIN, METHYLPARABEN, PROPYLPARABEN, CI 19140, SODIUM CHLORIDE, CI 15985.

  • WARNING

    1. Before use, perform a skin test on your arm and discontinue
    use if you have allergy symptoms or skin abnormalities.
    2. For external use only, avoid contact with eyes when used
    3. Keep out of reach of children

  • INSTRUCTIONS FOR USE

    Before using this Day Face Cream, Kindly remove all the impurities from your face. Apply and massage for sometimes.

  • INDICATIONS

    Before using this Day Face Cream, Kindly remove all the impurities from your face. Apply and massage for sometimes. The first result can be seen after 7 days.

  • DOSAGE

    For external use only, avoid contact with eyes when used

  • WARNING

    keep out of reach of children

  • PRINCIPAL DISPLAY PANEL

    7 DAYS WHITENING FACE CREAM

    1. Active Ingredients
    GLUTATHIONE 0.5%
    ALPHA-ARBUTIN 1%
    ALOE BARBADENSIS1.25%

    2.Purpose
    For Face Whitening and Moisturizing

    3.Inactive ingredients:
    AQUA, GLYCERIN, MINERAL OIL, HYDROXYACETOPHENONE, 1,2-HEXANEDIOL,BUTYLENE GLYCOL, PALMITIC ACID, STEARIC ACID, MYRISTIC ACID, LAURIC ACID, DIMETHICONE, NIACINAMIDE, GLYCERYL STEARATE, POLYSORBATE 60, Water, BUTYLENE GLYCOL, ANTHEMIS NOBILIS FLOWER EXTRACT, PORTULACA OLERACEA FLOWER/LEAF/STEM EXTRACT, PELARGONIUM GRAVEOLENS FLOWER/LEAF/STEM EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, TRANEXAMIC ACID, TITANIUM DIOXIDE, ALUMINA, TRIETHANOLAMINE, PEG-75 LANOLIN, PHENOXYETHANOL, ALLANTOIN, METHYLPARABEN, PROPYLPARABEN, CI 19140, SODIUM CHLORIDE, CI 15985.

    4.Warning
    1. Before use, perform a skin test on your arm and discontinue use if you have allergy symptoms or skin abnormalities.
    2. For external use only, avoid contact with eyes when used
    3. Keep out of reach of children

    LABEL

  • INGREDIENTS AND APPEARANCE
    7 DAYS WHITENING FACE CREAM 
    7 days whitening face cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84423-006
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALPHA-ARBUTIN (UNII: 72VUP07IT5) (ALPHA-ARBUTIN - UNII:72VUP07IT5) ALPHA-ARBUTIN0.5 mg  in 50 mg
    GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE0.25 mg  in 50 mg
    ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X) ALOE VERA LEAF0.625 mg  in 50 mg
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    PELARGONIUM GRAVEOLENS FLOWERING TOP (UNII: 1P36QZP48P)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TRANEXAMIC ACID (UNII: 6T84R30KC1)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PURSLANE (UNII: M6S840WXG5)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MYRISTIC ACID (UNII: 0I3V7S25AW)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84423-006-0150 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01607/01/2024
    Labeler - Guangzhou Kadiya Biotechnology Co.,,Ltd. (713172913)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Kadiya Biotechnology Co., Ltd.713172913manufacture(84423-006)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!