THE SKIN HOUSE HYALURONIC 6000 AMPOULE- sodium hyaluronate liquid

THE SKIN HOUSE HYALURONIC 6000 AMPOULE by

Drug Labeling and Warnings

THE SKIN HOUSE HYALURONIC 6000 AMPOULE by is a Otc medication manufactured, distributed, or labeled by NOKSIBCHO cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium Hyaluronate

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

anti-wrinkle function

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

apply proper amount and gently massage

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

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

THE SKIN HOUSE HYALURONIC 6000 AMPOULE 
sodium hyaluronate liquid

Product 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)