Label: THE SKIN HOUSE WRINKLE SNAIL SYSTEMCREAM- adenosine cream
- NDC Code(s): 73590-0032-1, 73590-0032-2
- 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 May 13, 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
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 - 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 SNAIL SYSTEMCREAM
adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0032 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:73590-0032-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/08/2020 2 NDC:73590-0032-2 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/08/2020 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(73590-0032)