Label: DO GOOD PURE REPAIR CENTELLA ESSENCE- niacinamide, adenosine liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 72058-060-01, 72058-060-02 - 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 26, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water, Propanediol, Alcohol, Methylpropanediol, Glycerin, 1,2-Hexanediol, Coconut Acid, Honey, Chondrus Crispus Extract, Saccharum Officinarum (Sugarcane) Extract, Centella Asiatica Leaf Extract, Citrus Aurantium Dulcis (Orange) Oil, Lactobacillus Ferment, Lavandula Angustifolia (Lavender) Oil, Hydrolyzed Corn Starch, Gaultheria Procumbens (Wintergreen) Leaf Extract, Ammonium Acryloyldimethyltaurate/VP Copolymer, Diphenyl Dimethicone, Butylene Glycol, C12-14 Pareth-12, Panthenol, Triethylhexanoin, Caprylyl Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Hydrogenated Lecithin, Sodium Hyaluronate, Citric Acid, Sodium Citrate, Sucrose, Xanthan Gum, Disodium EDTA
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DO GOOD PURE REPAIR CENTELLA ESSENCE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72058-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.5 g in 25 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 25 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propanediol (UNII: 5965N8W85T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72058-060-02 1 in 1 CARTON 01/02/2018 1 NDC:72058-060-01 25 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(72058-060)