Label: COXIR INTENSIVE EGF PEPTIDE- niacinamide, adenosine emulsion
- NDC Code(s): 73590-0072-1, 73590-0072-2
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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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, Butylene Glycol Dicaprylate/Dicaprate, Helianthus Annuus (Sunflower) Seed Oil, 1,2-Hexanediol, Glyceryl Stearate,
Arachidyl Alcohol, Cyclopentasiloxane, Polysorbate 60, Phenoxyethanol, Dimethicone, Diisostearyl Malate, Behenyl Alcohol, Cyclohexasiloxane, PEG-100 Stearate, Arachidyl Glucoside, Sorbitan Stearate, Hydrogenated Lecithin, Xanthan GUM, Tocopheryl Acetate, Allantoin, Carbomer, Ethylhexylglycerin, Disodium EDTA, Arginine, Sodium Hyaluronate, Parfum, Glycerin, Glucose, Tocopherol, Thymus Vulgaris (Thyme) Extract, Phaseolus Radiatus Meristem Cell Culture Extract, Panax ginseng culture extract, Camellia sinensis Callus Culture extracts, Malva Sylvestris (Mallow) Flower Extract, Buddleja Davidii Extract, Myrciaria Dubia Fruit Extract, Euterpe Oleracea Fruit Extract, Sodium Benzoate, Potassium Sorbate, Hydrolyzed Collagen, 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
niacinamide, adenosine emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0072 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2.0 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0072-2 1 in 1 CARTON 07/01/2021 1 NDC:73590-0072-1 100 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(73590-0072)
