Label: GD11 ADVANCED LAB ENERGY AMPOULE- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62171-080-01, 62171-080-02 - Packager: Coson 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 August 24, 2017
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Methylpropanediol, Human Cord Blood Cell Conditioned Media, Glycerin, Propanediol, Dipropylene Glycol, Glycereth-26, Trehalose, Betaine, Pentylene Glycol, Bis-PEG-18 Methyl Ether Dimethyl Silane, PEG-40 Hydrogenated Castor Oil, Butylene Glycol, Salvia Hispanica Seed Extract, Centella Asiatica Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Houttuynia Cordata Extract, Tromethamine, Fructooligosaccharides,Saccharide Hydrolysate,Panthenol,Dextrin,Ethylhexylglycerin,Pullulan,Gardenia Florida Fruit Extract, 1,2-Hexanediol,Disodium EDTA, Gardenia Jasminoides Fruit Extract, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Salix Alba (Willow) Bark Extract, Lactobacillus/Soybean Ferment Extract, Portulaca Oleracea Extract, Cinnamomum Cassia Bark Extract, Scutellaria Baicalensis Root Extract, Sodium Hyaluronate, Fragrance
- PURPOSE
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WARNINGS
Warnings: For external use only
Caution in usage 1. In case of having problems such as red rash, swollenness, itching, you need to consult a dermatologist. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis 3. Caution for treatment and keeping. - Keep it out of infants or children's reach. - Don't keep it exposed to the direct sunlight
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GD11 ADVANCED LAB ENERGY AMPOULE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62171-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.16 g in 8 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.003 g in 8 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Methylpropanediol (UNII: N8F53B3R4R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62171-080-02 5 in 1 CARTON 07/01/2017 1 NDC:62171-080-01 8 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 07/01/2017 Labeler - Coson Co., Ltd. (689835593) Registrant - Coson Co., Ltd. (689835593) Establishment Name Address ID/FEI Business Operations COSON Co., Ltd._Osan Plant 689847210 manufacture(62171-080)