Label: CELLSTIN AMPOULE BLACK- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72049-010-01, 72049-010-02 - Packager: Woojin DMC Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 29, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water,Glycerin,Dipropylene Glycol,Squalane, 1,2-Hexanediol,Sodium Hyaluronate,Macadamia Ternifolia Seed Oil, Leontopodium Alpinum Callus Culture Extract,Ethylhexylglycerin,Ascorbic Acid,Butylene Glycol,Impatiens Balsamina Flower Extract,Rosa Multiflora Fruit Extract,Lepidium Meyenii Root Extract,Eriobotrya Japonica Leaf Extract,Pachyrrhizus Erosus Root Extract,Aureobasidium Pullulans Ferment,Allantoin,Dimethicone,Dimethicone/Vinyl Dimethicone Crosspolymer, Laureth-23,Butylene Glycol,Sodium Polyacrylate,Hydrogenated Polydecene, Trideceth-6,Decylene Glycol,Caprylyl Glycol, Pentylene Glycol,Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Parfum
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CELLSTIN AMPOULE BLACK
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72049-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.2 g in 10 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.004 g in 10 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72049-010-02 4 in 1 CARTON 01/02/2018 1 NDC:72049-010-01 10 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2018 Labeler - Woojin DMC Co.,Ltd. (694444957) Registrant - Woojin DMC Co.,Ltd. (694444957) Establishment Name Address ID/FEI Business Operations Woojin DMC Co.,Ltd. 694444957 manufacture(72049-010)