THE SKIN HOUSE WRINKLE SNAIL SYSTEMCREAM- adenosine cream 
NOKSIBCHO cosmetic 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

adenosine

Snail Secretion Filtrate
Water
Butylene glycol
Dipropylene Glycol
Caprylic/Capric Triglyceride
1,2-Hexanediol
Olivoyl Hydrolyzed Wheat Protein
Glyceryl Oleate
Glyceryl Stearate
Glycerin
Orbignya Oleifera Seed Oil
Hydrogenated Polydecene
Phenoxyethanol
PEG-90M
Carbomer
Dimethicone
Cetearyl Alcohol
Arginine
Betaine
Xanthan GUM
Rosa Canina Fruit Oil
Solanum Lycopersicum (Tomato) Fruit Extract
Paeonia Lactiflora Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Leontopodium alpinum extract
Buddleja Davidii Extract
Buddleja Davidii Extract
Thymus Vulgaris (Thyme) Extract
Aloe Barbadensis Callus Culture Extract
Panax ginseng callus culture extract
Bambusa vulgaris Callus Culture extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Ethylhexylglycerin
Parfum

wrinkle care

keep out of reach of the children

apply proper amount to the skin

For external use only
When using this product

■ if the following symptoms occurs after use, stop use and consult with a skin specialist

red specks, swelling, itching

■ don’t use on the part where there is injury, eczema, or dermatitis

Keep out of reach of children

■ if swallowed, get medical help or contact a person control center immediately

label

THE SKIN HOUSE WRINKLE SNAIL SYSTEMCREAM 
adenosine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73590-0032
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73590-0032-1100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2020
2NDC:73590-0032-250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/08/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/08/2020
Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Establishment
NameAddressID/FEIBusiness Operations
NOKSIBCHO cosmetic Co., Ltd.690182175manufacture(73590-0032)

Revised: 5/2020
Document Id: a58e41a9-486a-6a1e-e053-2a95a90aff9b
Set id: a21f02ef-6251-139b-e053-2995a90aa0b3
Version: 2
Effective Time: 20200513
 
NOKSIBCHO cosmetic Co., Ltd.