OTC Medication Information: THE SKIN HOUSE Wrinkle CollagenEmulsion

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.

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
(click image for full-size original)

THE SKIN HOUSE WRINKLE COLLAGENEMULSION adenosine emulsion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0031
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ADENOSINE (ADENOSINE) ADENOSINE 0.04 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:73590-0031-1 130 mL in 1 BOTTLE None
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 Operations
NOKSIBCHO cosmetic Co., Ltd. 690182175 manufacture (73590-0031)

Revised: 03/2020 NOKSIBCHO cosmetic Co., Ltd.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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