Label: BANDHA WHO AND Y ZONE SERUM- niacinamide, adenosine liquid

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

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 September 23, 2020

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS

    NIACINAMIDE 2.0%
    ADENOSINE 0.04%

  • INACTIVE INGREDIENTS

    Dendropanax Morbiferus Leaf Extract, Water, Propanediol, 1,2-Hexanediol, Butylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, C12-14 Pareth 12, Allantoin, Astragalus Membranaceus Root Extract, Boswellia Serrata Extract, Melia Azadirachta Leaf Extract, Phyllanthus Emblica Extract , Trifolium Pratense (Clover) Flower Extract, Garcinia Cambogia Fruit Extract , Fragrance, Disodium EDTA, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Xanthan Gum, Sodium Hyaluronate, Lactobionic Acid

  • PURPOSE

    Brightening
    Anti-wrinkle

  • WARNINGS

    1. Please avoid use during periods of menstruation.
    2. Pregnant women should consult a specialist before using.
    3. For external use only
    4. Avoid contact with eyes.
    5. Discontinue use if signs of irritation or rashes appear.
    6. 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. Completely dry off your body after a shower
    2. Push the pump about 2 times and take an appropriate amount to the hand.
    3. Apply gently to desired areas (vulva, bikini line, etc.).

  • QUESTIONS

    +8227978088
    www.bandha.co.kr

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    BANDHA WHO AND Y ZONE SERUM 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80623-030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE1.0 g  in 50 mL
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.02 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propanediol (UNII: 5965N8W85T)  
    1,2-Hexanediol (UNII: TR046Y3K1G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80623-030-021 in 1 CARTON09/01/2020
    1NDC:80623-030-0150 mL in 1 BOTTLE; 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(80623-030)