FDA.reportPublic FDA data

IT RADIANT CC IN MELTING FOUNDATION

Manufacturer
F&CO Co., Ltd.
Effective date
2014-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:35:32

Label at a glance#

ProductIT RADIANT CC IN MELTING FOUNDATION BE15
Active ingredientTITANIUM DIOXIDE, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 12.93%, Ethylhexyl Methoxycinnamate 5.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water, Cyclopentasiloxane, Phenyl Trimethicone, Glycerin, Cyclohexasiloxane, Ceresin, Butylene Glycol, PEG-10 Dimethicone, Polyethylene, Niacinamide, Dicaprylyl Carbonate, Butylene Glycol Dicaprylate/Dicaprate, Pentaerythrityl Tetraethylhexanoate, Iron Oxides (CI 77492), PEG-32, Trimethiylsiloxyphenyl Dimethicone, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Pentylene Glycol, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Sorbitan Isostearate, Phenoxyethanol, Magnesium Sulfate, Iron Oxides (CI 77491), Dimethicone, Methyl Methacrylate Crosspolymer, Glyceryl Behenate, Polyglyceryl-6 Octastearate, Stearic Acid, Dimethicone Crosspolymer, Alumina, Triethoxycaprylylsilane, Fragrance(Parfum), Iron Oixdes (CI 77499), Ethylhexylglycerin, Adenosine, Disodium EDTA, Imperata Cylindrica Root Extract, Bisabolol, Helianthus Annuus (Sunflower) Seed Oil, Hibiscus Sabdariffa Flower Extract, PEG-8, Cassia Angustifolia Seed Polysaccharide, Centella Asiatica Extract, Carbomer, Methylparaben, Potassium Sorbate, Butylparaben, Ethylparaben, Propylparaben, Isobutylparaben

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

CAUTION

WARNINGS SECTION

CAUTION:
If redness or irritation occurs, discontinue use and consult a dermatologist. Do not use on broken skin. For external use only. Replace the cap after use. Keep out of reach of children Do not expose to heat or direct sunlight. Do not store at high temperatures. Avoid contact with eyes.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

How to Use

INDICATIONS & USAGE SECTION

How to Use: Use the enclosed sponge spread even and gently tap.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration:
Best blended with 28% water-based & 15% powder formula, this hydrating concealing cream foundation offers all-day moist, radiant finish that richly moisturizes and protects skin with anti-aging benefits.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Phenyl TrimethiconeINACTIVE INGREDIENTDR0K5NOJ4R1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-02069106-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
Water059QF0KO0RIACT
Phenyl TrimethiconeDR0K5NOJ4RIACT

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
7cee0024-ea4d-4793-b789-e4331f8f664baf2f2e7d-ef3a-412e-9d12-3bceb1fcc2392014-08-12WarningsExact identifier
spl id: 7cee0024-ea4d-4793-b789-e4331f8f664b
spl set id: af2f2e7d-ef3a-412e-9d12-3bceb1fcc239

Reported adverse events (FAERS/openFDA)#

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