THE SKIN HOUSE HYALURONIC 6000 AMPOULE- sodium hyaluronate liquid 
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.

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Drug Facts

Sodium Hyaluronate

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

anti-wrinkle function

keep out of reach of the children

apply proper amount and gently massage

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

for external use only

label

THE SKIN HOUSE HYALURONIC 6000 AMPOULE 
sodium hyaluronate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73590-0020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM6 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73590-0020-130 mL in 1 BOTTLE; Type 0: Not a Combination Product03/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/14/2020
Labeler - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Registrant - NOKSIBCHO cosmetic Co., Ltd. (690182175)
Establishment
NameAddressID/FEIBusiness Operations
NOKSIBCHO cosmetic Co., Ltd.690182175manufacture(73590-0020)

Revised: 3/2020
Document Id: a103df89-0437-f1d9-e053-2995a90a1dca
Set id: a103df05-5067-4324-e053-2995a90accd6
Version: 1
Effective Time: 20200316
 
NOKSIBCHO cosmetic Co., Ltd.