Label: DIAPIA HA AQUA SHINING MASK- niacinamide liquid

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

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Drug Label Information

Updated October 29, 2020

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  • ACTIVE INGREDIENT

    Niacinamide

  • INACTIVE INGREDIENT

    Water, Butylene Glycol, Glycereth-26, Glycerin, Methylpropanediol, 1,2-Hexanediol, Phenoxyethanol, Carbomer, Hydroxyethyl Urea, Triethanolamine, Dipotassium Glycyrrhizate, Allantoin, PEG/PPG-17/6 Copolymer, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Saccharide Isomerate, Xanthan Gum, Tetrasodium EDTA, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Vaccinium Angustifolium (Blueberry) Fruit Extract,

    Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Fragaria Chiloensis (Strawberry) Fruit Extract, Fragrance, Sodium Citrate, Citric Acid, Polyglutamic Acid, Hydroxyethylcellulose

  • PURPOSE

    Brightening, Moisturizing, Softening, Soothing

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Cleanse and dry face thoroughly.

    Open pouch, unfold mask and apply to face.

    Leave it for 10 - 20 minutes, remove the mask and tap slightly until essence

    absorbed.

  • WARNINGS

    1.Keep out of reach of children.

    2.Store in a cool, dry place and avoid direct sunlight.

    3.If abnormal symptoms occur after use, stop use and consult with a skin specialist.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DIAPIA HA AQUA SHINING MASK 
    niacinamide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71857-0013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71857-0013-124 mL in 1 POUCH; Type 0: Not a Combination Product10/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/30/2020
    Labeler - BSG H & B Co., Ltd. (694252895)
    Registrant - BSG H & B Co., Ltd. (694252895)
    Establishment
    NameAddressID/FEIBusiness Operations
    BSG H & B Co., Ltd.694252895manufacture(71857-0013) , label(71857-0013)
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