ILLUMINATING Treatment Mask

Manufacturer
SANSUNG LIFE & SCIENCE CO., LTD.
Effective date
2015-11-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:44:12

Label at a glance#

ProductILLUMINATING Treatment Mask
Active ingredientWitch Hazel
Label structure8 sections

Dosage and administration

Directions: 1) Clean and dry face. 2) Remove mask from package and gently unfold. 3) Place mask directly on skin, contouring it to fit the curves around the eyes, nose and mouth. 4) Leave on for 10-20 minutes. 5) Remove mask and gently pat the face with fingertips until the remaining serum is fully absorbed. *Suggested use is 2-3 times a week.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Hamamelis Virginiana (Witch Hazel) Water 0.1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Methylpropanediol, Glycerin, Butylene Glycol, Dipropylene Glycol, Niacinamide, Chamomilla Recutita (Matricaria) Flower Extract, Acer saccharum (Sugar Maple) Extract, Portulaca Oleracea Extract, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Betaine, Caprylyl Glycol, Ethylhexylglycerin, Xanthan Gum, Polysorbate 60, Sorbitan Isostearate, (-)-alpha-bisabolol, Fragrance, Sodium Hyaluronate, Artemisia Capillaris Flower Extract, Ecklonia Cava Extract, Houttuynia Cordata Extract, Ledum Palustre Extract, Saururus Chinensis Extract, Achillea Millefolium Extract, Arnica Montana Flower Extract, Artemisia Absinthium Extract, Gentiana Lutea Root Extract, Palmitoyl Tripeptide-5, Phenylethyl Resorcinol.

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warning: For external use only. Avoid contact with eyes. Not for human consumption. Discontinue use if irritation occurs. If irritation persists, consult a physician. Use immediately after opening. Store in cool and dry place. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Directions

INDICATIONS & USAGE SECTION

Directions: 1) Clean and dry face. 2) Remove mask from package and gently unfold. 3) Place mask directly on skin, contouring it to fit the curves around the eyes, nose and mouth. 4) Leave on for 10-20 minutes. 5) Remove mask and gently pat the face with fingertips until the remaining serum is fully absorbed. *Suggested use is 2-3 times a week.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: 1) Clean and dry face. 2) Remove mask from package and gently unfold. 3) Place mask directly on skin, contouring it to fit the curves around the eyes, nose and mouth. 4) Leave on for 10-20 minutes. 5) Remove mask and gently pat the face with fingertips until the remaining serum is fully absorbed. *Suggested use is 2-3 times a week.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cello packImage of cello pack

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69424-060-012020-01-31C16284748780-19d75b9d1-02c7-f424-e053-dadaa90a57ce37d02617-86c1-4e2d-8e08-8cebae6e54dd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69424-060-01ILLUMINATING Treatment Mask25 mL in 1 CELLO PACKPATCH252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69424-060ILLUMINATING TREATMENT MASK (WITCH HAZEL) PATCH [SANSUNG LIFE & SCIENCE CO., LTD.]2Legacy NDC, 1 package rows20151125_37d02617-86c1-4e2d-8e08-8cebae6e54dd.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Witch HazelACTIVE INGREDIENT101I4J0U342
WITCH HAZELACTIVE MOIETY101I4J0U342
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69424-06069424-060-01

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
Witch Hazel101I4J0U34ACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
1e0aecba-90fc-4cb9-9250-df0de301cfb437d02617-86c1-4e2d-8e08-8cebae6e54dd2015-11-25WarningsExact identifier
spl id: 1e0aecba-90fc-4cb9-9250-df0de301cfb4
spl set id: 37d02617-86c1-4e2d-8e08-8cebae6e54dd

Reported adverse events (FAERS/openFDA)#

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