FDA.reportPublic FDA data

THE SKIN HOUSE HYALURONIC 6000 AMPOULE

Manufacturer
NOKSIBCHO cosmetic Co., Ltd.
Effective date
2020-03-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:03:59

Label at a glance#

ProductTHE SKIN HOUSE HYALURONIC 6000 AMPOULE
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Hyaluronate

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

anti-wrinkle function

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply proper amount and gently massage

WARNINGS SECTION

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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73590-0020-12025-01-30C16284748780-12cef2736-a45f-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73590-0020-1THE SKIN HOUSE HYALURONIC 6000 AMPOULE30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73590-0020THE SKIN HOUSE HYALURONIC 6000 AMPOULE (SODIUM HYALURONATE) LIQUID [NOKSIBCHO COSMETIC CO., LTD.]1Legacy NDC, 1 package rows20200317_a103df05-5067-4324-e053-2995a90accd6.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73590-002073590-0020-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONATE SODIUMYSE9PPT4THACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a103df89-0437-f1d9-e053-2995a90a1dcaa103df05-5067-4324-e053-2995a90accd62020-03-16WarningsExact identifier
spl id: a103df89-0437-f1d9-e053-2995a90a1dca
spl set id: a103df05-5067-4324-e053-2995a90accd6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.