Label: DO GOOD PERFECTING AQUA GE L MOISTURIZER- niacinamide, adenosine gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72058-010-01, 72058-010-02 - Packager: WOOREE Colourone Co.,Ltd
- 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 February 5, 2018
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Dipropylene Glycol, Glycerin, Butylene Glycol, Cyclopentasiloxane, Dimethicone, 1,2-Hexanediol, Panthenol, Polysorbate 60, Squalane, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Caprylyl Glycol, Sodium Polyacrylate, Tromethamine, Polyacrylamide, Chondrus Crispus Extract, Dimethicone/Vinyl Dimethicone Crosspolymer, PEG-240/HDI Copolymer Bis-Decyltetradeceth-20 Ether, Saccharum Officinarum (Sugarcane) Extract, C13-14 Isoparaffin, Glyceryl Acrylate/Acrylic Acid Copolymer, Fragrance(Parfum), Disodium EDTA, Laureth-7, Alchemilla Vulgaris Extract, Xylitylglucoside, Anhydroxylitol, Caprylic/Capric Triglyceride, Potassium Laurate, Tocopherol, Xylitol, Hydrogenated Lecithin, Ceramide NP
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DO GOOD PERFECTING AQUA GE L MOISTURIZER
niacinamide, adenosine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72058-010 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) Dipropylene Glycol (UNII: E107L85C40) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72058-010-02 1 in 1 CARTON 01/02/2018 1 NDC:72058-010-01 50 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 - WOOREE Colourone Co.,Ltd (694492496) Registrant - WOOREE Colourone Co.,Ltd (694492496) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(72058-010)