Label: THE HAYAN CHERRY BLOSSOM BRIGHTENING ESSENCE- niacinamide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 59078-303-01, 59078-303-02 - Packager: TONYMOLY CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated June 1, 2016
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredient: Prunus Yedoensis Flower Extract, Methylpropanediol, Cyclomethicone, Hydrogenated Ethylhexyl Olivate, PPG-14 Butyl Ether, C14-22 Alcohols, Olea Europaea (Olive) Fruit Oil, Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Pelargonium Graveolens Flower Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Eucalyptus Globulus Leaf Oil, Cymbopogon Martini Oil, Michelia Alba Flower Oil, 1,2-Hexanediol, Polyglyceryl-2 Stearate, Glyceryl Stearate, Stearyl Alcohol, Dimethicone/Vinyl Dimethicone Crosspolymer, C12-20 Alkyl Glucoside, Cetearyl Alcohol, Hydrogenated Olive Oil Unsaponifiables, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Maltodextrin, Cyanocobalamin, Sodium Citrate, Citric Acid, Tromethamine, Disodium EDTA
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Use
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
THE HAYAN CHERRY BLOSSOM BRIGHTENING ESSENCE
niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59078-303 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.1 g in 55 mL Inactive Ingredients Ingredient Name Strength Methylpropanediol (UNII: N8F53B3R4R) Cyclomethicone (UNII: NMQ347994Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59078-303-02 1 in 1 CARTON 05/01/2016 1 NDC:59078-303-01 55 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2016 Labeler - TONYMOLY CO.,LTD (688216798) Registrant - TONYMOLY CO.,LTD (688216798) Establishment Name Address ID/FEI Business Operations TONYMOLY CO.,LTD 688216798 manufacture(59078-303)