NDC | 72001-0018-1 |
Set ID | 807e9934-69bf-5e1b-e053-2991aa0a974d |
Category | HUMAN OTC DRUG LABEL |
Packager | Banobagi Co., Ltd. |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number | PART347 |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water, Methylpropanediol, Glycerin, Caprylic/Capric Triglyceride, Hydrolyzed Collagen, Centella Asiatica Extract, Bambusa Vulgaris Water, Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Thioctic Acid, Hydroxypropyl Cyclodextrin, Tremella Fuciformis (Mushroom) Extract, Pseudoalteromonas Ferment Extract, Hydrolyzed Wheat Protein, Hydrolyzed Soy Protein, Tripeptide-10 Citrulline, Tripeptide-1, Lecithin, Dimethicone, Polysorbate 60, Xanthan Gum, Tocopheryl Acetate, Sorbitan Sesquioleate, Allantoin, Panthenol, Polyacrylate-13, Polyisobutene, Polysorbate 20, Carbomer, Adenosine, Potassium Hydroxide, 1,2-Hexanediol, Hydroxyacetophenone, Disodium EDTA, Fragrance
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
1. If abnormal symptoms or side effects such as red spots, swelling, or itching are present in the cosmetics or in the direct sunlight after use, consult a specialist
2. Do not use in wounded areas
3. Precautions for storage and handling
- Keep out of reach of children
- Keep away from direct sunlight
4. Avoid the use of eye area
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BANOBAGI ANTI-OXIDANTINJECTION MASK
adenosine, glycerin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72001-0018 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 g GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 2.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72001-0018-1 250 g in 1 BOX; Type 0: Not a Combination Product 01/28/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part347 01/28/2019 Labeler - Banobagi Co., Ltd. (694436539) Registrant - Banobagi Co., Ltd. (694436539) Establishment Name Address ID/FEI Business Operations C&TECH CORPORATION 688204698 manufacture(72001-0018) Establishment Name Address ID/FEI Business Operations Banobagi Co., Ltd. 694436539 label(72001-0018)