THE SKIN HOUSE EGF COLLAGEN AMPOULE

Manufacturer: NOKSIBCHO cosmetic Co., Ltd.
Effective date: 2020-03-14
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 EGF COLLAGEN AMPOULE

Active ingredientGLYCYRRHIZINATE DIPOTASSIUM

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hydrolyzed Collagen (GLYCYRRHIZINATE DIPOTASSIUM)

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
Propylene Glycol
Hydrolyzed Collagen
Dipotassium Glycyrrhizate
Sodium Citrate
Glyceryl Acrylate/Acrylic Acid Copolymer
PVM/MA Copolymer
Carbomer
Xanthan GUM
Hydrogenated Lecithin
sh-Oligopeptide-1
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

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73590-0019-1	2025-01-30	C162847	48780-1	2cef2736-b52e-d83d-e063-dadaa90ab31f	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73590-0019-1	THE SKIN HOUSE EGF COLLAGEN AMPOULE	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73590-0019	THE SKIN HOUSE EGF COLLAGEN AMPOULE (HYDROLYZED COLLAGEN (GLYCYRRHIZINATE DIPOTASSIUM)) LIQUID [NOKSIBCHO COSMETIC CO., LTD.]	1	Legacy NDC, 1 package rows	20200317_a0cc3b31-0e7a-0937-e053-2995a90adb74.zip

Products#

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

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

THE SKIN HOUSE EGF COLLAGEN AMPOULE
Hydrolyzed Collagen (GLYCYRRHIZINATE DIPOTASSIUM)
WATER
BUTYLENE GLYCOL
GLYCYRRHIZINATE DIPOTASSIUM
GLYCYRRHIZIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73590-0019	73590-0019-1

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
GLYCYRRHIZINATE DIPOTASSIUM	CA2Y0FE3FX	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a0cc3b6a-c6ab-8410-e053-2995a90ae5e9			a0cc3b31-0e7a-0937-e053-2995a90adb74	2020-03-14	Warnings	Exact identifier spl id: a0cc3b6a-c6ab-8410-e053-2995a90ae5e9 spl set id: a0cc3b31-0e7a-0937-e053-2995a90adb74

Reported adverse events (FAERS/openFDA)#

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