Label: DIAPIA ADL EVER-CURE SERUM- 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 1, 2021

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  • ACTIVE INGREDIENT

    Niacinamide, Adenosine

  • INACTIVE INGREDIENT

    Water, Glycerin, Sodium Hyaluronate, Hydrogenated Polydecene, Centella Asiatica Extract, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Polysorbate 80, Cyclopentasiloxane, PEG/PPG-18/18 Dimethicone, Curcuma Longa (Tumeric) Root Extract, Opuntia Humifusa Extract, Morus Alba Leaf Extract, Phenoxyethanol, Allantoin, Curcuma Longa (Turmeric) Root Powder, Fragrance, Allium Hookeri Extract, Propolis Extract, Portulaca Oleracea Extract

  • PURPOSE

    Brightening & Anti-wrinkle care, Soothing, Moisturizing, Relieving itching skin

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Put the appropriate amount onto face and gently massage until fully 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 ADL EVER-CURE SERUM 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71857-0011
    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:71857-0011-150 mL in 1 BOTTLE; 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(71857-0011) , label(71857-0011)