Label: DPC WHITENING BOOSTER MASK- niacinamide liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated August 18, 2017

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  • ACTIVE INGREDIENT

    NIACINAMIDE

  • INACTIVE INGREDIENT

    Water
    Dipropylene glycol
    Methylpropanediol
    Alcohol
    Glycerin
    Sodium Hyaluronate
    1,2-Hexanediol
    Biosaccharide Gum-1
    Boswellia Serrata Resin Extract
    Butylene Glycol
    Allantoin
    Dipotassium Glycyrrhizate
    Beta-Glucan
    Hydroxyethylcellulose
    Acrylates/c10-30 alkyl acrylate crosspolymer
    Simmondsia Chinensis (Jojoba) Seed Oil
    Citrus Limon (Lemon) Fruit Extract
    Citrus Aurantium Dulcis (Orange) Fruit Water
    Oryza Sativa (Rice) Extract
    Citrus Aurantifolia (Lime) Fruit Extract
    Citrus Paradisi (Grapefruit) Fruit Extract
    Caprylic/capric Triglyceride
    Hydrogenated Lecithin
    Phytosteryl/octyldodecyl Lauroyl Glutamate
    Ceramide NP
    Polyglyceryl-10 Laurate
    Polyglyceryl-10 Myristate
    Arginine
    Dehydroacetic acid
    Chlorphenesin
    Disodium EDTA
    Glycyrrhiza Glabra (Licorice) Root Extract
    Zingiber Officinale (Ginger) Root Extract
    Schizandra Chinensis Fruit Extract
    Coptis Japonica Root Extract
    Camellia Sinensis Leaf Extract
    Caprylyl Glycol
    Fragrance

  • PURPOSE

    Skin Protectant - Intensive Whitening

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    1. After cleansing wipe water and apply skin lotion on face.
    2. Apply the mask evenly over the face for 10-20 minutes and remove.
    3. Pad the left over residue lightly to absorb.

  • WARNINGS

    For external use only.
    Avoid contact with eyes. Not for human consumption.
    Discontinue use if irritation occurs.
    If irritation persists, consult a physician.

  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    DPC WHITENING BOOSTER MASK 
    niacinamide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71673-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    WATER (UNII: 059QF0KO0R)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71673-0003-15 in 1 PACKAGE07/01/2017
    120 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2017
    Labeler - MSCO (689039838)
    Registrant - MSCO (689039838)
    Establishment
    NameAddressID/FEIBusiness Operations
    MSCO689039838label(71673-0003)
    Establishment
    NameAddressID/FEIBusiness Operations
    CNF CO.,LTD.689852175manufacture(71673-0003)
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