Cover Perfection Concealer Foundation 02

Manufacturer
The Saem International Co., Ltd. | Cosmecca Korea Co., Ltd.
Effective date
2018-07-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:53:40

Label at a glance#

ProductCover Perfection Concealer Foundation 02
Active ingredientTitanium Dioxide, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 14.82%, Zinc Oxide 6.30%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Cyclopentasiloxane, Phenyl Trimethicone, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Trimethylsiloxysilicate, PEG-10 Dimethicone, Niacinamide, Butylene Glycol Dicaprylate/Dicaprate, Glycerin, Talc, CI 77492, Dimethicone/Vinyl Dimethicone Crosspolymer, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Sodium Chloride, Disteardimonium Hectorite, Aluminum Hydroxide, Dimethicone, Stearic Acid, Beeswax, Silica, 1,2-Hexanediol, Triethoxycaprylylsilane, Portulaca Oleracea Extract, CI 77491, Panthenol, Hydroxyacetophenone, Triethyl Citrate, Polymethylsilsesquioxane, Polyhydroxystearic Acid, Butyl Avocadate, Adansonia Digitata Seed Extract, CI 77499, Phyllostachis Bambusoides Juice, Fragrance, Disodium EDTA, Adenosine, Ethylhexyl Palmitate, Lecithin, Isopropyl Palmitate, Isostearic Acid, Lavandula Angustifolia (Lavender) Flower Extract, Castanea Crenata (Chestnut) Shell Extract, Polyglyceryl-3 Polyricinoleate, Uncaria Gambir Extract, Sanguisorba Officinalis Root Extract, Nelumbo Nucifera Flower Extract, Pelargonium Graveolens Extract, Cinnamomum Zeylanicum Bark Extract, Caprylic/Capric Triglyceride, Alcohol, Phenoxyethanol, Pistacia Lentiscus (Mastic) Gum, Aloe Barbadensis Leaf Extract, Biosaccharide Gum-1, Camellia Sinensis Leaf Extract, Ethylhexylglycerin, Amber Extract, Caprylyl Glycol, Propyl Gallate

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:

Using the slanted tip of the applicator, dot or sweep the product onto skin and gently blend in with fingers using a pressing motion. For extra touch-up, use the pointy tip to apply over blemishes and pat with fingers to blend well.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70341-69570341-695-01, 70341-695-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
7e86b14b-4650-4057-bab7-84484321bc31a34d9a43-a3f6-4ac1-90cc-154a8a05c5022019-12-27WarningsExact identifier
spl set id: a34d9a43-a3f6-4ac1-90cc-154a8a05c502

Reported adverse events (FAERS/openFDA)#

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