Label: DIAPIA CICA RELIEF PORE PAD- niacinamide, adenosine liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated December 10, 2021

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  • ACTIVE INGREDIENT

    Niacinamide

    adenosine

  • INACTIVE INGREDIENT

    Water
    Butylene Glycol
    Gluconolactone
    Tromethamine
    Dipropylene Glycol
    Hydroxyacetophenone
    1,2-Hexanediol
    Polyglyceryl-10 Laurate
    Caprylyl Glycol
    Centella Asiatica Extract
    Betaine
    Allantoin
    Trehalose
    Ethylhexylglycerin
    Disodium EDTA
    Citric Acid
    Ammonium Acryloyldimethyltaurate/VP Copolymer
    Dipotassium Glycyrrhizate
    Tocopherol

  • PURPOSE

    Brightening, anti wrinkle care

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    gently wipe the entire face except around the eyes and mouth with the embossing side of the pad

    tap, using other side of the pad (smooth side) to organize the skin texture and absorb remaining contents

    make sure to close the lid after use

  • 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 CICA RELIEF PORE PAD 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71857-0020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    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:71857-0020-1135 mL in 1 JAR; Type 0: Not a Combination Product12/10/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/01/2021
    Labeler - BSG H & B Co., Ltd. (694252895)
    Registrant - BSG H & B Co., Ltd. (694252895)
    Establishment
    NameAddressID/FEIBusiness Operations
    BSG H & B Co., Ltd.694252895label(71857-0020) , manufacture(71857-0020)