Leaders Mediu 2 Step Double Effect Brightening Mask

Manufacturer: SANSUNG LIFE & SCIENCE CO., LTD.
Effective date: 2015-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:42:14

Label at a glance#

ProductLeaders Mediu 2 Step Double Effect Brightening Mask

Active ingredientWitch Hazel

Label structure8 sections

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, Butylene Glycol, Glycerin, Niacinamide , Acer saccharum (Sugar Maple) extract, Portulaca Oleracea Extract, 1,2-Hexanediol, Chamomilla Recutita (Matricaria) Flower Extract, Arnica Montana Flower Extract, Artemisia Absinthium Extract, Betaine, Hydroxyethyl acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acetyl Tetrapeptide-11, Achillea Millefolium Extract, Gentiana Lutea Root Extract, Lactobacillus, Leuconostoc Ferment Filtrate, Cocos Nucifera (Coconut) Fruit Extract, Caprylyl Glycol, Ethylhexylglycerin, Saururus Chinensis Extract, Xanthan Gum, Ledum Palustre Extract, Ecklonia Cava Extract, Artemisia Capillaris Flower Extract, Houttuynia Cordata Extract, Malva Sylvestris (Mallow) Extract, Mentha Piperita (Peppermint) Leaf Extract, Primula Veris Extract, Alchemilla Vulgaris Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Achillea Millefolium Extract, Fragrance.

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

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indication and usage: 1. After cleansing and applying toner, attached the upper mask to fit your face shape. 2. Align the center part of the lower mask with the center of your chin and pull the mask up slowly towards your ears. Attached around the ears. 3. Leave on for about 20 minutes and remove both the upper and lower masks. Gently pat your face with fingertips to help the remaining essence to completely absorb into your skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: 2-3 times a week.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cello pack

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69424-180-01	2020-01-31	C162847	48780-1	9d75b9d0-4549-f424-e053-dadaa90a57ce	5535f40a-4e6b-40a1-8e11-ee665945b9b7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69424-180-01	Leaders Mediu 2 Step Double Effect Brightening Mask	28 g in 1 CELLO PACK	PATCH	28		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69424-180	LEADERS MEDIU 2 STEP DOUBLE EFFECT BRIGHTENING MASK (WITCH HAZEL) PATCH [SANSUNG LIFE & SCIENCE CO., LTD.]	1	Legacy NDC, 1 package rows	20150409_5535f40a-4e6b-40a1-8e11-ee665945b9b7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Witch Hazel	ACTIVE INGREDIENT	101I4J0U34	1
WITCH HAZEL	ACTIVE MOIETY	101I4J0U34	1
Butylene Glycol	INACTIVE INGREDIENT	3XUS85K0RA	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

Leaders Mediu 2 Step Double Effect Brightening Mask
Witch Hazel
Water
Butylene Glycol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69424-180	69424-180-01

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
Name	UNII	Kind
Witch Hazel	101I4J0U34	ACTIB
Water	059QF0KO0R	IACT
Butylene Glycol	3XUS85K0RA	IACT

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 ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
Butylene Glycol	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TRANSDERMAL	8.12 mg		Exact identifier — unii candidate 2 equally ranked IID candidates
Butylene Glycol	BUTYLENE GLYCOL	3XUS85K0RA	SYSTEM / TOPICAL		1400 mg	Exact 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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
59b149ed-9858-4d2f-94f2-b7b505724311			5535f40a-4e6b-40a1-8e11-ee665945b9b7	2015-04-09	Warnings	Exact identifier spl id: 59b149ed-9858-4d2f-94f2-b7b505724311 spl set id: 5535f40a-4e6b-40a1-8e11-ee665945b9b7

Reported adverse events (FAERS/openFDA)#

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