NDC | 60565-230-01, 60565-230-02 |
Set ID | a086b3bb-cc5a-4983-b2c9-b26ff795244f |
Category | HUMAN OTC DRUG LABEL |
Packager | DN Company Co.,Ltd. |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water, Glycerin, Cetyl Ethylhexanoate, Caprylic/Capric Triglyceride, Dicaprylyl Carbonate, Pentylene Glycol, Cetearyl Alcohol, Glyceryl Stearate, Dimethicone, Polysorbate 60, 1,2-Hexanediol, Caprylic/Capric/Myristic/Stearic Triglyceride, Stearic Acid, PEG-100 Stearate, DI-C12-13 Alkyl Malate, Sorbitan Sesquioleate, Caprylyl Glycol, Hydroxyethyl Acrylate/Sodium AcryloyldimethylTaurate Copolymer, Polyacrylamide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, C13-14 Isoparaffin, Fragrance (Parfum), Tromethamine, Alcohol Denat., Xanthan Gum, Disodium EDTA, Laureth-7, Hydrogenated Lecithin, Phytosphingosine, Saccharide Isomerate, BHT, Potassium Cetyl Phosphate, Helianthus Annuus (Sunflower) Seed Oil, Sodium Ascorbyl Phosphate, Centella Asiatica Extract, Citric Acid, Sodium Citrate
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EASYDEW EX REPAIR CONTROL RENEWAL MOISTURE
niacinamide, adenosine, nepidermin creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60565-230 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 Nepidermin (UNII: TZK30RF92W) (HUMAN EPIDERMAL GROWTH FACTOR - UNII:TZK30RF92W) Nepidermin 0.0001 g in 50 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:60565-230-02 1 in 1 CARTON 02/01/2018 1 NDC:60565-230-01 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 02/01/2018 Labeler - DN Company Co.,Ltd. (688369859) Registrant - DN Company Co.,Ltd. (688369859) Establishment Name Address ID/FEI Business Operations Cosmax, Inc. 689049693 manufacture(60565-230)