Label: THE SKIN HOUSE HYALURONIC 6000 AMPOULE- sodium hyaluronate liquid
- NDC Code(s): 73590-0020-1
- 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 16, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Sodium Hyaluronate
Phenoxy ethanol
Glycerin
Butylene glycol
Betaine
Alcohol
1,2-Hexanediol
PPG-26-Buteth-26
PEG-40 Hydrogenated Castor Oil
Arginine
Squalane
Camellia Sinensis Leaf Extract
Hydrolyzed Collagen
Dipotassium Glycyrrhizate
Sodium Citrate
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
PVM/MA Copolymer
Carbomer
Xanthan GUM
Solanum Lycopersicum (Tomato) Fruit Extract
Paeonia Lactiflora Bark/Sap Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Myrciaria Dubia Fruit Extract
Euterpe Oleracea Fruit Extract
Ardisia Crispa Extract
Rubus Coreanus Fruit Extract
Phellinus Linteus Extract
Aloe Barbadensis Leaf Extract
Nelumbo Nucifera Leaf Extract
Citric Acid
Adenosine
Disodium EDTA
Panax ginseng culture extract
Caprylyl Glycol
Phaseolus Radiatus Seed Extract
Ethylhexylglycerin
Gardenia Florida Fruit Extract
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 HYALURONIC 6000 AMPOULE
sodium hyaluronate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73590-0020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 6 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73590-0020-1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/14/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/14/2020 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(73590-0020)