Label: DPC AURA 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 17, 2017

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  • ACTIVE INGREDIENT

    NIACINAMIDE

  • INACTIVE INGREDIENT

    Water
    Glycerin
    Butylene Glycol
    Sodium Hyaluronate
    1,2-Hexanediol
    Allantoin
    Dipotassium Glycyrrhizate
    Trehalose
    Hydroxyethylcellulose
    Carbomer
    PEG-60 Hydrogenated Castor Oil
    Glyceryl Acrylate/Acrylic Acid Copolymer
    Propylene Glycol
    PVM/MA Copolymer
    Panthenol
    Diamond powder
    Simmondsia Chinensis (Jojoba) Seed Oil
    Anthemis Nobilis Flower Extract
    Jasminum Officinale (Jasmine) Flower Water
    Lilium Tigrinum Extract
    Arnica Montana Flower Extract
    Arginine
    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
    Citrus Grandis (Grapefruit) Seed Extract
    Acorus Calamus Root Extract
    Perilla Ocymoides Leaf Extract
    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 AURA BOOSTER MASK 
    niacinamide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71673-0001
    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:71673-0001-15 in 1 PACKAGE07/01/2017
    125 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(71673-0001)
    Establishment
    NameAddressID/FEIBusiness Operations
    CNF CO.,LTD.689852175manufacture(71673-0001)
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