SNAIL BEE HIGH CONTENT MASK PACK

Manufacturer
BENTON KOREA | Ezekiel Cosmetics Co.
Effective date
2016-03-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:27:47

Label at a glance#

ProductSNAIL BEE HIGH CONTENT MASK PACK
Active ingredientGlycerin
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Glycerin 4.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Camellia Sinensis Leaf Water, Snail Secretion Filtrate, Butylene Glycol, Arbutin, Sodium Hyaluronate, Zanthoxylum Piperitum Fruit Extract,Pulsatilla Koreana Extract,Usnea Barbata (Lichen) Extract, Diospyros Kaki Leaf Exrtact,Salix Alba (Willow) Bark Extract ,Plantago Asiatica Exrtact,Laminaria Digitata Exrtact,Ulmus Campestris (Elm) Extract, Althaea Rosea Root Extract,Aloe Barbadenis Leaf Extract, Betaine, Bacillus Ferment,Azelaic Acid, Xanthan Gum, Human Oligo Peptode-1, Beta-Glucan, Panthenol, Allantoin, Adenosine, Bee Venom

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. In case of having following symptoms after using this, you’re advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: Prepare your skin with skin toner after washing your face. Open the packaging and place the mask gently over the face: make sure it adheres to the face. After 20-30 minutes remove the mask, then pat the leftover ingredients gently into the skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Take an adequate amount of this product.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69998-030-012022-04-11C16284748780-19d75b9d0-a486-f424-e053-dadaa90a57ce2485b6ea-4b09-4daa-b9ab-05d37cf2e7f7
69998-030-012020-01-31C16284748780-19d75b9d0-a486-f424-e053-dadaa90a57ce2485b6ea-4b09-4daa-b9ab-05d37cf2e7f7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX1
GLYCERINACTIVE MOIETYPDC6A3C0OX1
ArbutinINACTIVE INGREDIENTC5INA23HXF1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1

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
69998-03069998-030-01

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
GlycerinPDC6A3C0OXACTIB
Butylene Glycol3XUS85K0RAIACT
ArbutinC5INA23HXFIACT

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
b2597eca-5c5d-4bd9-9fcf-f153b9a879e02485b6ea-4b09-4daa-b9ab-05d37cf2e7f72022-04-11WarningsExact identifier
spl set id: 2485b6ea-4b09-4daa-b9ab-05d37cf2e7f7

Reported adverse events (FAERS/openFDA)#

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