FDA.reportPublic FDA data

MEDITERRANEAN OLIVE BRIGHTENING MASK

Manufacturer
SANSUNG LIFE & SCIENCE CO., LTD.
Effective date
2015-05-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:42:37

Label at a glance#

ProductMEDITERRANEAN OLIVE 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, 1,2-Hexanediol, Chamomilla Recutita (Matricaria) Flower Extract, Cocos Nucifera (Coconut) Fruit Extract, Betaine, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Portulaca Oleracea Extract, Acer Saccharum (Sugar Maple) Extract, Ethylhexylglycerin, Caprylyl Glycol, Arnica Montana Flower Extract, Xanthan Gum, Olea Europaea (Olive) Fruit Oil, Fragrance, Artemisia Capillaris Flower Extract, Houttuynia Cordata Extract, Ecklonia Cava Extract, Artemisia Absinthium Extract, Saururus Chinensis Extract, Achillea Millefolium Extract, Ledum Palustre Extract, Morus Alba Bark Extract, Veronica Officinalis Extract, Melissa Officinalis Leaf Extract, Malva Sylvestris (Mallow) Extract, Alchemilla Vulgaris Extract, Alcohol, Primula Veris Extract, Mentha Piperita (Peppermint) Leaf Extract, Gentiana Lutea Root Extract, Hydrogenated Lecithin, Panthenol, Niacinamide, Tocopheryl Acetate, Retinyl Palmitate, Biotin, Ascorbic Acid, Folic Acid, Dipotassium Glycyrrhizate, Ceramide 3, Glyceryl Linolenate, Glyceryl Linoleate, Glyceryl Arachidonate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 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: Step 1. Take out mask from pouch and remove protective film from either side of the mask. Step 2. Apply to cleansed face and smooth to fit facial contours. Step 3. Leave mask on face for 20~25 minutes. Step 4. Discard mask and lightly pat face to help absorb serum into skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: 2-3 times a week. Each mask is for one time use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cello packImage of cello pack

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codem.site.naver.com/097fsmediterranean olive brightening mask cello pack.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69424-250-012020-01-31C16284748780-19d75b9d0-71bf-f424-e053-dadaa90a57cec06f1799-da64-4f98-803b-5d3af089964f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69424-250-01MEDITERRANEAN OLIVE BRIGHTENING MASK30 mL in 1 CELLO PACKPATCH301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69424-250MEDITERRANEAN OLIVE BRIGHTENING MASK (WITCH HAZEL) PATCH [SANSUNG LIFE & SCIENCE CO., LTD.]1Legacy NDC, 1 package rows20150529_c06f1799-da64-4f98-803b-5d3af089964f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Witch HazelACTIVE INGREDIENT101I4J0U341
WITCH HAZELACTIVE MOIETY101I4J0U341
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
69424-25069424-250-01

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 / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 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
0cbbab80-94c8-49cb-914e-bb889e978d54c06f1799-da64-4f98-803b-5d3af089964f2015-05-29WarningsExact identifier
spl id: 0cbbab80-94c8-49cb-914e-bb889e978d54
spl set id: c06f1799-da64-4f98-803b-5d3af089964f

Reported adverse events (FAERS/openFDA)#

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