STEM CELL WHITENING SERUM - niacinamide liquid 
Medon Co., Ltd

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.

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Drug Facts

active ingredient: adenosine

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

to improve wrinkle

keep out of reach of the children

- cleansing the skin
- dispense an amount on the palm
- smooth gently over the face and tap softly to absorb

- do not use when you feel itching
- do not swallow
- clean the skin before use

for external use only

package label
STEM CELL WHITENING SERUM 
niacinamide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76071-3001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.02 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76071-3001-13 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/06/2011
Labeler - Medon Co., Ltd (557802532)
Registrant - Medon Co., Ltd (557802532)
Establishment
NameAddressID/FEIBusiness Operations
Medon Co., Ltd557802532manufacture

Revised: 4/2011
Document Id: 14cfdf50-cac6-4c94-83d8-ec7663ef920f
Set id: c1cb5366-e5d4-488e-947f-c30e0e2c6936
Version: 1
Effective Time: 20110406
 
Medon Co., Ltd