W Lab BLOSSOM WHITE CUSHION 21 Blossom Light

Manufacturer
WOW VENTURES | Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory
Effective date
2016-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:22:01

Label at a glance#

ProductW Lab BLOSSOM WHITE CUSHION 21 Blossom Light
Active ingredientTitanium Dioxide, Octinoxate, Octisalate, Octocrylene, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Titanium Dioxide 11.0%, Ethylhexyl Methoxycinnamate 7.0%, Ethylhexyl Salicylate 4.8%, Octocrylene 2.0%, Zinc Oxide 2.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Rosa Damascena Flower Water, Butylene Glycol, Cyclopentasiloxane, Cyclohexasiloxane, Glycerin, C12-15 Alkyl benzoate, PEG-30 Dipolyhydroxystearate, Niacinamide, Trimethylsiloxysilicate, PEG-10 Dimethicone, Sodium Chloride, Quaternium-18 Bentonite, Iron Oxides (CI 77492), Dimethicone, Iron Oxides (CI 77491), Ozokerite, Copernicia Cerifera (Carnauba) Wax, Triethoxycaprylylsilane, Chlorphenesin, Iron Oxides (CI 77499), Aluminum Hydroxide (CI 77002), Phenoxyethanol, Perfume, Water, Adenosine, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Trehalose, Melaleuca Alternifolia (Tea Tree) Leaf Water, Rubus Idaeus (Raspberry) Fruit Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Bambusa Vulgaris Water, Lilium Candidum Bulb Extract, Xylitylglucoside, Propanediol, Rosmarinus Officinalis (Rosemary) Leaf Water, Propylene Glycol, Melissa Officinalis Flower/Leaf/Stem Water, Anhydroxylitol, Alcohol, Xylitol, Origanum Majorana Leaf Extract, Leontopodium Alpinum Extract, 1,2-Hexanediol, Lavandula Angustifolia (Lavender) Flower, Phyllanthus Emblica Fruit Extract, Angelica Archangelica Root Extract, Centella Asiatica Extract, Salicornia Herbacea Extract, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Vulgaris Extract, Arnica Montana Flower Extract, Portulaca Oleracea Extract, Chamomilla Recutita (Matricaria) Flower Extract, Vitex Agnus Castus Extract, Plankton Extract, Camellia Japonica Flower Extract, Viola Tricolor Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Potassium Sorbate, Sodium Hyaluronate, Citric Acid, Sodium Benzoate, Euterpe Oleracea Fruit Extract, Arginine Ferulate, Calendula Officinalis Flower Extract, Hydrolyzed Hyaluronic Acid

PURPOSE

OTC - PURPOSE SECTION

Purpose: Make Up Base(Coverage), Brightening, Skin Protectant , Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: 1. Stop using the product if there is any of the following abnormal symptoms appeared after use and consult with your dermatologist as continued use can worsen the symptoms. A) if there are red spots, swelling, itchiness, or irritation B) if the above symptoms appear around the skin to which the product has been applied, after being exposed to direct sunlight. 2. Do not apply the product to any parts of the skin with wound, eczema, or dermatitis. 3. Precautions on storage and handling. A) Make sure to close the cap after use. B) Keep out of the reach of children and babies. C) Do not keep the product in a hot or cold place or a place getting direct sunlight.

DESCRIPTION

DESCRIPTION SECTION

Indications & usage: Take an adequate amount and apply it to to your face by tapping with a puff gently and evenly.

Dosage & Administration: Apply it to your face by tapping with a puff gently and evenly.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809483660334GTIN-13: 8809483660334
EAN-13: 8809483660334
GTIN storage (14 digits): 08809483660334
w lab blossom white cushion 21 blossom light carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69894-470-022024-12-05C16284748780-19d75b9d0-e554-f424-e053-dadaa90a57ceb45c9be2-fee9-4d75-aef2-da2a67fbb857
69894-470-022020-01-31C16284748780-19d75b9d0-e554-f424-e053-dadaa90a57ceb45c9be2-fee9-4d75-aef2-da2a67fbb857

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69894-47069894-470-01, 69894-470-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
28822809-2757-babe-e063-6394a90aa863b45c9be2-fee9-4d75-aef2-da2a67fbb8572024-12-05WarningsExact identifier
spl set id: b45c9be2-fee9-4d75-aef2-da2a67fbb857

Reported adverse events (FAERS/openFDA)#

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