Snail Essential EX Origin BB 21 Light Beige

Manufacturer
The Saem International Co., Ltd. | Kolmar Korea Co., Ltd.
Effective date
2018-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:54:20

Label at a glance#

ProductSnail Essential EX Origin BB 21 Light Beige
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: TITANIUM DIOXIDE 12.92%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ZINC OXIDE 0.98%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Cyclopentasiloxane, Butylene Glycol, Dipropylene Glycol, Talc, Caprylic/Capric Triglyceride, Pentaerythrityl Tetraisostearate, Cetyl PEG/PPG-10/1 Dimethicone, Arbutin, Phenyl Trimethicone, Disteardimonium Hectorite, Magnesium Sulfate, Iron Oxides(CI 77492), Dimethicone, Polyglyceryl-4 Isostearate, Triethoxycaprylylsilane, Phenoxyethanol, Fragrance, Iron Oxides(CI 77491), Palmitic Acid, Polyglyceryl-6 Polyricinoleate, Iron Oxides(CI 77499), Ethylhexylglycerin, Portulaca Oleracea Extract, Tocopheryl Acetate, Hydroxyethylcellulose, Aminopropyl Dimethicone, Methicone, Polymethylsilsesquioxane, Adenosine, Alumina, Snail Secretion Filtrate, Silica, Ethyl Hexanediol, 1,2-Hexanediol, Ceramide NP, Glycyrrhiza Glabra (Licorice) Root Extract, Hippophae Rhamnoides Fruit Extract, Sodium Hyaluronate, Soluble Collagen, Aloe Barbadensis Leaf Juice, Paeonia Lactiflora Root Extract, Xanthan Gum, Cnidium Officinale Root Extract, Pueraria Thunbergiana Root Extract, Hyaluronic Acid

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

For external use only

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.

4. Keep out of reach of babies and children.

DESCRIPTION

DESCRIPTION SECTION

Uses:

Helps prevent sunburn.

Directions:

Use after your skincare routine. Apply an appropriate amount evenly on the face along skin's texture and gently tap for better coverage.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70341-63070341-630-01, 70341-630-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
0016d471-762c-4e92-bd21-0000d2f1199638e296c3-2db8-4a46-9e6f-cde4398bd0bc2019-12-30WarningsExact identifier
spl set id: 38e296c3-2db8-4a46-9e6f-cde4398bd0bc

Reported adverse events (FAERS/openFDA)#

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