U-max Wrinkle Serum

Dosage form: liquid
Ingredients: ADENOSINE 0.04mL in 100mL
Labeler: VS Shinbi Co., Ltd.
NDC Code: 50795-1001

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.

Drug Facts

active ingredient: adenosine

inactive ingredient:  water, glycerin, disodium EDTA, carbomer, houttuynia cordata extract, xanthium strumarium fruit extract, angelica gigas root extract, glycyrrhiza glabra root extract, hydrolyzed soybean extract, artemisia vulgaris extract, actinidia chinensis fruit extract, musa sapientum fruit extract, aloe barbadensis leaf extract, perfurm, portulaca oleracea extract, salcornia herbacea extract, laminaria japonica extract, taraxacum officinale leaf extract, citrus paradisi seed oil, cellulose gum, betaine, peg-60 hydrogenated castor oil, triethanolamine, alcohol, methylparaben, cyclopentasioxane/dimethicone, cyclomethicone

skin protectant (anti-wrinkle)

keep out of reach of the children

- apply only for skin
- apply 2 or 3 times a day with 5~6ml
- massage with your finger over 2 min and let them dry


- keep out of eyes, ears and mouth
- if contact occurs, rinse away with plenty of cold water

- for external use only

U-MAX WRINKLE SERUM 
adenosine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50795-1001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ADENOSINE (ADENOSINE) ADENOSINE0.04 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
EDETATE DISODIUM 
HOUTTUYNIA CORDATA FLOWERING TOP 
XANTHIUM STRUMARIUM FRUIT 
SOLANUM LYCOPERSICUM 
ANGELICA GIGAS ROOT 
GLYCYRRHIZA GLABRA 
ARTEMISIA VULGARIS ROOT 
KIWI FRUIT 
BANANA 
ALOE VERA LEAF 
PURSLANE 
SALICORNIA EUROPAEA 
LAMINARIA JAPONICA 
TARAXACUM OFFICINALE 
CITRUS PARADISI SEED 
BETAINE 
POLYOXYL 60 HYDROGENATED CASTOR OIL 
ALCOHOL 
METHYLPARABEN 
CYCLOMETHICONE 
Packaging
#Item CodePackage Description
1NDC:50795-1001-150 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other06/04/2012
Labeler - VS Shinbi Co., Ltd. (557817055)
Registrant - VS Shinbi Co., Ltd. (557817055)
Establishment
NameAddressID/FEIOperations
VS Shinbi Co., Ltd.557817055manufacture

Revised: 06/2012
 
VS Shinbi Co., Ltd.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide
(web5)