It Radiant CC Cover Light Beige

Manufacturer
F&CO Co., Ltd. | Cosmax, Inc
Effective date
2017-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:10:25

Label at a glance#

ProductIt Radiant CC Cover Light Beige
Active ingredientTitanium Dioxide, Zinc Oxide, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: Titanium Dioxide 7.76%, Zinc Oxide 4.90%, Ethylhexyl Methoxycinnamate 5.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Water, Phenyl Trimethicone, Caprylyl Methicone, Butylene Glycol, Cyclopentasiloxane, Glycerin, Methyl Trimethicone, Cyclomethicone, PEG-10 Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Niacinamide, 1,2-Hexanediol, Tridecyl Trimellitate, Butylene Glycol Dicaprylate/Dicaprate, Maltitol, Polypropylsilsesquioxane, VP/Hexadecene Copolymer, Cyclohexasiloxane, Magnesium Sulfate, Disteardimonium Hectorite, Dipentaerythrityl Hexa C5-9 Acid Esters, Glyceryl Tribehenate/Isostearate/Eicosandioate, Sorbitan Isostearate, Tribehenin, Aluminum Hydroxide, Iron Oxides (CI 77492), Dimethicone, Stearic Acid, Triethoxycaprylylsilane, Iron Oxides (CI 77491), Chamomilla Recutita (Matricaria) Flower Extract, Centella Asiatica Extract, Dimethicone Crosspolymer, Ethylhexylglycerin, Glyceryl Caprylate, Fragrance(Parfum), Adenosine, Synthetic Fluorphlogopite, Iron Oxides (CI 77499), Disodium EDTA, Mica (CI 77019), Argania Spinosa Kernel Oil, Oenothera Biennis (Evening Primrose) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Caprylic/Capric Triglyceride, Sodium Hyaluronate, Hydrogenated Lecithin, Aspalathus Linearis Extract, Centaurea Cyanus Flower Water, Lilium Candidum Flower Water, Paeonia Albiflora Root Extract, Phenoxyethanol, Ceramide NP, Hibiscus Sabdariffa Flower Extract, Tilia Europaea Flower Extract, Portulaca Oleracea Extract, Lavandula Angustifolia (Lavender) Flower Extract, Lavandula Angustifolia (Lavender) Oil

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: After skin care, evenly spread moderate amount on skin. * Softly spreads on skin where hand touches. Doesn’t become thick or turns yellow although severely coated on skin. Everyone can easily use the product.

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
69106-47069106-470-01, 69106-470-02

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
cc270b3d-b51a-43cd-8983-c7513e719f754f6f559b-efd3-4f94-ba9b-ff6a339e57082017-11-08WarningsExact identifier
spl id: cc270b3d-b51a-43cd-8983-c7513e719f75
spl set id: 4f6f559b-efd3-4f94-ba9b-ff6a339e5708

Reported adverse events (FAERS/openFDA)#

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