Label: VITA SNAIL- niacinamide, adenosine cream
- NDC Code(s): 73590-0061-1, 73590-0061-2
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 3, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Snail Secretion Filtrate, Caprylic/Capric Triglyceride, Butylene glycol, Olivoyl Hydrolyzed Wheat Protein, Cetearyl Alcohol, Glyceryl Oleate, Glyceryl Stearate, Cetearyl Alcohol, 1,2-Hexanediol, Lactose, Cellulose, Hydroxypropyl Methylcellulose Jojoba Esters, Iron Oxide Red, Tocopheryl Acetate, Ascorbyl Palmitate, Carbomer, Arginine, PEG-90M, Xanthan GUM, Butyrospermum Parkii (Shea) Butter, Sodium Polyacrylate, Hydrogenated polydecene, Trideceth-6, Centella Asiatica Extract, Dipotassium Glycyrrhizate, Squalane, Hydrolyzed Collagen, Betaine, Vaccinium Angustifolium (Blueberry) Fruit Extract, Euterpe Oleracea Fruit Extract, Ethylhexylglycerin, Citrus Nobilis (Mandarin Orange) Peel Extract, Cupressus Sempervirens Leaf/Stem Extract, Hedera Helix (Ivy) Leaf/Stem Extract, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Litsea Cubeba Fruit Oil, Ribes Nigrum (Black Currant) Leaf Extract
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITA SNAIL
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0061 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 MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Butylene glycol (UNII: 3XUS85K0RA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) Glyceryl Oleate (UNII: 4PC054V79P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0061-2 1 in 1 CARTON 03/01/2021 1 NDC:73590-0061-1 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 03/01/2021 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(73590-0061)