It Radiant CC Color Base Mint

Manufacturer
F&CO Co., Ltd. | Cosmax, Inc
Effective date
2017-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:10:24

Label at a glance#

ProductIt Radiant CC Color Base Mint
Active ingredientTitanium Dioxide, Zinc Oxide, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Titanium Dioxide 4.13%, Zinc Oxide 4.90%, Ethylhexyl Methoxycinnamate 5.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Water, Cyclopentasiloxane, Cyclohexasiloxane, Diphenylsiloxy Phenyl Trimethicone, Butylene Glycol Dicaprylate/Dicaprate, Dipropylene Glycol, Glycerin, PEG-10 Dimethicone, Niacinamide, Pentylene Glycol, Undecane, Tridecane, Caprylyl Methicone, Disteardimonium Hectorite, Tribehenin, Magnesium Sulfate, Phenoxyethanol, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Aluminum Hydroxide, Cetearyl Dimethicone/Vinyl Dimethicone Crosspolymer, Chromium Oxide Greens (CI 77288), Stearic Acid, Dimethicone, Synthetic Fluorphlogopite, Ethylhexylglycerin, Triethoxycaprylylsilane, Adenosine, Fragrance(Parfum), Disodium EDTA, Mica (CI 77019), Trehalose, Methyl Methacrylate Crosspolymer, Butylene Glycol, Tocopherol, Silica, Helianthus Annuus (Sunflower) Seed Oil, Sodium Hyaluronate, Centella Asiatica Extract, Citrus Aurantifolia (Lime) Fruit Extract, Portulaca Oleracea Extract, Mentha Rotundifolia Leaf Extract

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Sunscreen

WARNINGS

WARNINGS SECTION

WARNINGS: 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.

INDICATION AND USAGE

DESCRIPTION SECTION

INDICATION AND USAGE: Evenly spread moderate amount on skin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-45069106-450-01, 69106-450-02

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
23a46460-3f00-44f7-99ce-e8401c242eea23a9d528-2ea0-4fc3-947c-4d60a4e8a9852017-11-08WarningsExact identifier
spl id: 23a46460-3f00-44f7-99ce-e8401c242eea
spl set id: 23a9d528-2ea0-4fc3-947c-4d60a4e8a985

Reported adverse events (FAERS/openFDA)#

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