FDA.reportPublic FDA data

IT RADIANT CC CUSHION

Manufacturer
F&CO Co., Ltd.
Effective date
2014-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:35:30

Label at a glance#

ProductIT RADIANT CC CUSHION BE20
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 7.16%, Ethylhexyl Methoxycinnamate 7.0%, Ethylhexyl Salicylate 3.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water, Butylene Glycol, Cyclopentasiloxane, Glycerin, Dimethicone, Cyclohexasiloxane, Pentylene Glycol, Niacinamide, Butylene Glycol Dicaprylate/Dicaprate, Dicaprylyl Carbonate, Phenyl Tirmethicone, PEG-10 Dimethicone, Triceteareth-4 Phosphate, Iron Oxides (CI 77492), Glycol Stearate, Phenoxyethanol, Glyceryl Stearate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Potassium Cetyl Phosphate, Polysorbate 60, PEG-2 Stearate, PEG-100 Stearate, Silica, Mica (CI 77019), Iron Oxides (CI 77491), Aluminum Hydroxide, Carbomer, Triethoxycaprylylsilane, Sodium Acrylate/Sodium Acryloyldimethicone Taurate Copolymer, Tromethamine, Fragrance(Parfum), Ethylhexylglycerin, Isohexadecane, Iron Oxides (CI 77499), Adenosine, Polysorbate 80, Disodium EDTA, Tremella Fuciformis (Mushroom) Extract, Saccharide Isomerate, Imperata Cylindrica Root Extract, Nelumbo Nucifera Flower Extract, Prunus Serrulata Flower Extract, Nymphaea Alba Flower Extract, Rosa Hybrid Flower Extract, Iris Versicolor Extract, Lilium Candidum Bulb Extract, Leontopodium Alpinum Flower/Leaf Extract, Rose Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Freesia Refracta Extract, Narcissus Pseudo-Narcissus (Daffodil) Flower Extract, PEG-8, Ethyl Hexanediol, Maltodextrin, Xanthan Gum, Orthosiphon Stamineus Leaf Extract, Sodium Citrate, Citric Acid, Potassium Sorbate, Phospholipids, Whey Protein, Lactose, Sodium Dehydroacetate

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 enclosed sponge to apply the product for light touch-ups or the entire face evenly.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration:
This moisture recharging CC Cushion is formulated with 55% water base helps complete a flawless, luminous complexion and ensures color builds into fine, even layers with a refreshing finish.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-06069106-060-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

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
22037846-fd28-448b-93f2-ab4deeb4ffe54c431701-ff8a-459a-b8d2-98539443c5c42014-08-13WarningsExact identifier
spl id: 22037846-fd28-448b-93f2-ab4deeb4ffe5
spl set id: 4c431701-ff8a-459a-b8d2-98539443c5c4

Reported adverse events (FAERS/openFDA)#

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