THE SKIN HOUSE Wrinkle System Essence

Manufacturer
NOKSIBCHO cosmetic Co., Ltd.
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:26

Label at a glance#

ProductTHE SKIN HOUSE Wrinkle System Essence
Active ingredientADENOSINE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

adenosine

INACTIVE INGREDIENT SECTION

Water
Glycerin
Butylene glycol
Cyclomethicone
Squalane
Hydrogenated Polydecene
Sodium Hyaluronate
Dimethicone
Glyceryl Acrylate/Acrylic Acid Copolymer
Propylene Glycol
Betaine
Macadamia Integrifolia Seed Oil
Methyl Glucose Sesquistearate
Arachidyl Glucoside
Lecithin
Caprylic/Capric Triglyceride
PEG-10 Dimethicone/Vinyl Dimethicone Crosspolymer
Panthenol
Hydrolyzed Collagen
Cetearyl Alcohol
PEG-100 Stearate
Glyceryl Stearate
PEG-60 Hydrogenated Castor Oil
Sorbitan Isostearate
Polysorbate 80
Butyrospermum Parkii (Shea Butter)
Stearic Acid
Carbomer
Arginine
Solanum Lycopersicum (Tomato) Fruit Extract
Paeonia Lactiflora Bark/Sap Extract
Lonicera Japonica (Honeysuckle) Flower Extract
Dipotassium Glycyrrhizate
Disodium EDTA
Snail Secretion Filtrate
Panax ginseng callus culture extract
Bambusa vulgaris Callus Culture extract
Aloe vera Callus Culture extract
Leontopodium alpinum extract
Thymus Vulgaris (Thyme) Extract
Buddleja Davidii Extract
Theobroma Cacao (Cocoa) Extract
Gardenia Florida Fruit Extract
Phenoxyethanol
Ethylhexylglycerin
CI 19140
CI 15985
Parfum

OTC - PURPOSE SECTION

wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply proper amount to the skin

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ADENOSINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73590-0034-1THE SKIN HOUSE Wrinkle System Essence50 mL in 1 BOTTLELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73590-0034THE SKIN HOUSE WRINKLE SYSTEM ESSENCE (ADENOSINE) LIQUID [NOKSIBCHO COSMETIC CO., LTD.]1Current NDC, Legacy NDC, 1 package rows20200331_a2211d4f-4411-18bf-e053-2995a90a4494.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73590-003473590-0034-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ADENOSINEK72T3FS567ACTIB

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
THE SKIN HOUSE Wrinkle System EssenceADENOSINENOKSIBCHO cosmetic Co., Ltd.a2211d4f-4411-18bf-e053-2995a90a44942020-03-31WarningsExact identifier
ndc (package): 73590-0034-1
ndc (product): 73590-0034
ndc11 (package): 73590003401
spl id: a2211d4f-4412-18bf-e053-2995a90a4494
spl set id: a2211d4f-4411-18bf-e053-2995a90a4494

Reported adverse events (FAERS/openFDA)#

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