Label: BANDHA YOU AND FACE MOISTURE- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 80623-040-01, 80623-040-02 - Packager: DKCOSTECH
- 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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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Water, Dendropanax Morbiferus Leaf Extract, Propandeiol, Cyclomethicone, Cyclopentasil, Phenyl Trimethicone, Niacinamide, Cyclohexasiloxane,
Cetyl Ethylhexanoate, Glyceryl Stearate, Peg-150 Distearate, Dimethicone/Vinyl Dimethicone Crsspolymer, Cetyl Alcohol, Cabomer, Polysorbate 80, Polyacylate-13, Butylene Glycol, Tromethamine, Artemisia Vulgaris Extract, Ethylhexylglycerin, Oenothera Biennis(Evening Primrose)Oil,
Betaine, Stearyl Alcohol, Allantoin, Xanthan Gum, Panthenol, Perfume, Polyisobutene, 1,2-Hexanediol, Tocopheryl Acetate, Adenosine, Disodium EDTA, Myristyl Alcohol, Hydrolyzed, Sodium Hyaluronate, Polysorbane 20, Sorbitan Isostearate, Garcinia Cambogia Fruit Extract, Boswellia Serrata Extract, Trifolium Pratense(CLOVER) Extract, Melia Azadirachth Leaf Extract, Phyllanthus Emblica Extract, Astragalus Membranaceus Root Extract - PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BANDHA YOU AND FACE MOISTURE
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80623-040 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 1.0 g in 50 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propanediol (UNII: 5965N8W85T) CYCLOMETHICONE (UNII: NMQ347994Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80623-040-02 1 in 1 CARTON 09/01/2020 1 NDC:80623-040-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2020 Labeler - DKCOSTECH (695504288) Registrant - DKCOSTECH (695504288) Establishment Name Address ID/FEI Business Operations HANSCOS Co.,Ltd. 688494423 manufacture(80623-040)