NDC | 71760-020-01, 71760-020-02 |
Set ID | b207b8de-8804-4280-8a51-dccf19223984 |
Category | HUMAN OTC DRUG LABEL |
Packager | ENKOREA, Inc. |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Butylene Glycol, Glycerin, Panax Ginseng Root Extract, Hydrolyzed Collagen, Beta-Glucan, Panthenol, Tourmaline, Diamond Powder, Xanthan Gum, Carbomer, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Althaea Rosea Flower Extract, Nymphaea Alba Root Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Portulaca Oleracea Extract, Hydroxyacetophenone, Polysorbate 80, 1,2-Hexanediol, Caprylyl Glycol, Potassium Sorbate, Sodium Benzoate, Triethanolamine, Disodium EDTA, Fragrance
- PURPOSE
-
WARNINGS
WARNINGS : 1. When you see reddish spot, swellings or itchiness, irritations or other side effects on your skin, during and /or after using the product, consult specialists. 2. Do not use the product for wounded areas, etc. 3. Caution in strage and handling a. It should be kept out of the reach of the children. b. It should be kept out of direct sunlight. 4. Use it avoiding around the eyes.
- KEEP OUT OF REACH OF CHILDREN
- USES
- DIRECTIONS
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RED GINSENG BRIGHTENING MASK PACK
niacinamide, adenosine patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71760-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.50 g in 25 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 25 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71760-020-02 5 in 1 CARTON 12/01/2017 1 NDC:71760-020-01 25 g in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2017 Labeler - ENKOREA, Inc. (694841643) Registrant - ENKOREA, Inc. (694841643) Establishment Name Address ID/FEI Business Operations ENKOREA, Inc. 694841643 manufacture(71760-020)