Label: COXIR INTENSIVE EGF PEPTIDE SERUM- niacinamide, adenosine liquid
- NDC Code(s): 73590-0073-1, 73590-0073-2
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 July 14, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Water(Aqua), Butylene glycol, Glycerin, Alcohol, Propylene Glycol, 1,2-Hexanediol, PEG/PPG-18/4 Copolymer, Betaine, Phenoxyethanol, Triethanolamine, Carbomer, Allantoin, Ethylhexylglycerin, Glyceryl Acrylate/Acrylic Acid Copolymer, Parfum, PVM/MA Copolymer, Dipropylene Glycol, Thymus Vulgaris (Thyme) Extract, Camellia sinensis Callus Culture extracts, Bambusa Vulgaris Callus Culture Extract, Malva Sylvestris (Mallow) Flower Extract, Leontopodium alpinum extract, Snail Secretion Filtrate, Hydrolyzed Collagen, Sodium Benzoate, Potassium Sorbate, Citric Acid, Caprylyl Glycol, Punica Granatum Fruit Extract, Panax Ginseng Root Extract, Carthamus Tinctorius (Safflower) Flower Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Solanum Lycopersicum (Tomato) Fruit Extract, Nelumbo Nucifera Seed Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Lilium Tigrinum Extract, Chrysanthemum Indicum Flower Extract, Tropolone, Copper Tripeptide-1, Oligopeptide-1
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COXIR INTENSIVE EGF PEPTIDE SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0073 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 Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0073-2 1 in 1 CARTON 07/01/2021 1 NDC:73590-0073-1 50 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 07/01/2021 Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175) Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175) Establishment Name Address ID/FEI Business Operations NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture(73590-0073)
