Label: COXIR INTENSIVE EGF PEPTIDE TONER- niacinamide, adenosine liquid
- NDC Code(s): 73590-0074-1, 73590-0074-2
- Packager: NOKSIBCHO cosmetic 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 July 14, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Water(Aqua), Butylene glycol, Alcohol, 1,2-Hexanediol, Glycerin, Betaine, Phenoxyethanol, PPG-26-Buteth-26, Ethoxydiglycol, PEG-40 Hydrogenated Castor Oil, Panthenol, Ethylhexylglycerin, Parfum, Tocopheryl Acetate, Sodium Hyaluronate, Thymus Vulgaris (Thyme) Extract, Phaseolus Radiatus Meristem Cell Culture Extract, Panax ginseng culture extract, Hydrolyzed Collagen, Camellia sinensis Callus Culture extracts, Malva Sylvestris (Mallow) Flower Extract, Buddleja Davidii Extract, Sodium Benzoate, Snail Secretion Filtrate, Potassium Sorbate, Citric Acid, Caprylyl Glycol, Myrciaria Dubia Fruit Extract, Euterpe Oleracea Fruit Extract, 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, Copper Tripeptide-1, Tropolone, 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 TONER
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0074 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 3.0 g in 150 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.06 g in 150 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Alcohol (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0074-2 1 in 1 CARTON 07/01/2021 1 NDC:73590-0074-1 150 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(73590-0074)
