Label: BANDHA FOR AND MASK- niacinamide, adenosine patch

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

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Drug Label Information

Updated September 23, 2020

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  • ACTIVE INGREDIENTS

    NIACINAMIDE 2.0%
    ADENOSINE 0.04%

  • INACTIVE INGREDIENTS

    Water, Dendropanax Morbiferus Leaf Extract, Propanediol, Glycerin, 1,2-Hexanediol, Butylene Glycol, betaine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Xanthan Gum, Aloe Barbadensis Leaf Extract, Astragalus Membranaceus Root Extract, Boswellia Serrata Extract, Melia Azadirachta Leaf Extract, Phyllanthus Emblica Extract, Trifolium Pratense (Clover) Flower Extract, Garcinia Cambogia Fruit Extract, Allantoin, Disodium EDTA, Fragrance, Sodium Hyaluronate

  • PURPOSE

    Brightening
    Anti-wrinkle

  • WARNINGS

    1. For external use only
    2. Avoid contact with eyes.
    3. Discontinue use if signs of irritation or rashes appear.
    4. Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    ■ Helps brighten skin tone.
    ■ Helps prevent wrinkle problem.

  • Directions

    1. After cleansing your face,
    2. Leave it on for 20 minutes.
    3. Gently remove the mask and pat the remaining essence into your face.

  • QUESTIONS

    +8227978088
    www.bandha.co.kr

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    BANDHA FOR AND MASK 
    niacinamide, adenosine patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80623-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.56 g  in 28 g
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.01 g  in 28 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propanediol (UNII: 5965N8W85T)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80623-010-0210 in 1 CARTON09/01/2020
    1NDC:80623-010-0128 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/01/2020
    Labeler - DKCOSTECH (695504288)
    Registrant - DKCOSTECH (695504288)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANSCOS Co.,Ltd.688494423manufacture(80623-010)
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