Label: THE SKIN HOUSE WRINKLE COLLAGENEMULSION- adenosine emulsion
- NDC Code(s): 73590-0031-1
- Packager: NOKSIBCHO cosmetic Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 30, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
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 - 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 COLLAGENEMULSION
adenosine emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0031 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:73590-0031-1 130 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(73590-0031)