Label: THE SKIN HOUSE WRINKLE SYSTEM EYECREAM- adenosine cream
- NDC Code(s): 73590-0035-1
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 Label Information
Updated March 31, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Butylene glycol
Sodium Hyaluronate
Cetyl Ethylhexanoate
Cyclomethicone
Stearic Acid
Isohexadecane
Butylene Glycol Dicaprylate/Dicaprate
Cetearyl Alcohol
Beeswax
Sorbitan Stearate
Squalane
1,2-Hexanediol
Glycerin
Arachidyl Alcohol
Behenyl Alcohol
Arachidyl Glucoside
Hydrolyzed Collagen
Polysorbate 60
Glyceryl Stearate
Dimethicone
Arginine
Tocopheryl Acetate
Limnanthes Alba (Meadowfoam) Seed Oil
Solanum Lycopersicum (Tomato) Fruit Extract
Paeonia Lactiflora Bark/Sap Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Allantoin
Panthenol
Disodium EDTA
Snail Secretion Filtrate
Panax Ginseng Root Extract
Bambusa Vulgaris Leaf/Stem Extract
Aloe Barbadensis Leaf Extract
Leontopodium alpinum extract
Thymus Vulgaris (Thyme) Extract
Buddleja Davidii Extract
Ethylhexylglycerin
Parfume - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
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
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
THE SKIN HOUSE WRINKLE SYSTEM EYECREAM
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0035 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0035-1 40 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/31/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/08/2020 Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175) Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175) Establishment Name Address ID/FEI Business Operations NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture(73590-0035)