THE SKIN HOUSE WRINKLE COLLAGENEMULSION- adenosine emulsion 
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

Water
Glycerin
Cetyl Ethylhexanoate
Mineral Oil
Hydrogenated Polydecene
Squalane
Sodium Hyaluronate
Butylene glycol
Cyclomethicone
1,2-Hexanediol
Methyl Glucose Sesquistearate
Arachidyl Glucoside
Lecithin
Glyceryl Stearate
Caprylic/Capric Triglyceride
Macadamia Integrifolia Seed Oil
Hydrolyzed Collagen
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
Betaine
Sorbitan Isostearate
Polysorbate 80
PEG-100 Stearate
Stearic Acid
Dimethicone
Lanolin
Water
Glycoproteins
Aloe Barbadensis Leaf Extract
Arginine
Cetearyl Alcohol
Allantoin
Dipropylene Glycol
Carbomer
Paeonia Lactiflora Bark/Sap Extract
Lilium Tigrinum Extract
Nelumbium Speciosum Flower Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Chrysanthemum Indicum Flower Extract
Cucurbita Pepo (Pumpkin) Fruit Extract
Solanum Lycopersicum (Tomato) Fruit Extract
Tocopheryl Acetate
Xanthan GUM
Disodium EDTA
Phenoxyethanol
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 COLLAGENEMULSION 
adenosine emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73590-0031
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:73590-0031-1130 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(73590-0031)

Revised: 3/2020
Document Id: a21f14df-a276-3791-e053-2a95a90a6b59
Set id: a21f1539-0022-3797-e053-2a95a90a5b92
Version: 1
Effective Time: 20200330
 
NOKSIBCHO cosmetic Co., Ltd.