Label: STEM CELL WHITENING SERUM- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 76071-3001-1 - Packager: Medon Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 6, 2011
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
inactive ingredient: water, human bone marrow stem cell conditioned media, butylene glycol, glycerin, alcohol denat, beta-glucan, sodium hyaluronate, hamamelis virginiana leaf extract, betaine, peg-60 hydrogenated castor oil, polyglutamic acid, lecithin, carnosine, glutathione, zanthoxylum piperitum fruit extract, pulsatilla koreana extract, usnea barbata extract, 1,2-hexanediol, caprylyl glycol, fragrance, disodium edta, oligopeptide-28, sh-decapeptide-7, caffeoyl tripeptide-1, sh-pentapeptide-198, sh-octapeptide-4, acetyl hexapeptide-22, acetyl hexapeptide-8
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STEM CELL WHITENING SERUM
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76071-3001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 0.02 mL in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) BETADEX (UNII: JV039JZZ3A) HYALURONATE SODIUM (UNII: YSE9PPT4TH) HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) BETAINE (UNII: 3SCV180C9W) POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) CARNOSINE (UNII: 8HO6PVN24W) GLUTATHIONE (UNII: GAN16C9B8O) ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251) USNEA BARBATA (UNII: D6DVA9TCAP) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76071-3001-1 3 mL in 1 SYRINGE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/06/2011 Labeler - Medon Co., Ltd (557802532) Registrant - Medon Co., Ltd (557802532) Establishment Name Address ID/FEI Business Operations Medon Co., Ltd 557802532 manufacture