3CE Tinted moisture cushion CC 001

Manufacturer
Nanda Co., Ltd | Cosmax, Inc.
Effective date
2016-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:38

Label at a glance#

Product3CE Tinted moisture cushion CC 001
Active ingredientTitanium Dioxide, Octinoxate, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Titanium Dioxide 8.9%, Ethylhexyl Methoxycinnamate 6.7%, Ethylhexyl Salicylate 4.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Cyclopentasiloxane, Cyclohexasiloxane, Dimethicone, Butylene Glycol, Butylene Glycol Dicaprylate/Dicaprate, PEG-8 Dimethicone, Glycerin, Niacinamide, Pentylene Glycol, Trimethylsiloxysilicate, Methyl Methacrylate Crosspolymer, Neopentyl Glycol Diheptanoate, Dimethicone/Vinyl DimethiconeCrosspolymer, Diphenylsiloxy Phenyl Trimethicone, Cetyl PEG/PPG-10/1 Dimethicone, PEG-8, Iron Oxides (CI 77492), Magnesium Sulfate, DisteardimoniumHectorite, Vinyl Dimethicone/MethiconeSilsesquioxaneCrosspolymer, SorbitanIsostearate, Phenoxyethanol, Mica (CI 77019), Stearic Acid, Alumina, Fragrance(Parfum), Iron Oxides (CI 77491), DimethiconeCrosspolymer, Triethoxycaprylylsilane, Ethylhexylglycerin, Iron Oxides (CI 77499), Adenosine, Disodium EDTA, Hydrogenated Castor Oil Isostearate, Hydrolyzed Hyaluronic Acid, AnastaticaHierochuntica Extract, Alcohol, GentianaLutea Root Extract, AchilleaMillefolium Extract, Artemisia Absinthium Extract, Arnica Montana Flower Extract, Lactobacillus Ferment, Potassium Sorbate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

CAUTION

WARNINGS SECTION

CAUTION: 1. Discontinue use and consult a doctor when - your skin irritates, swells, itches, shows spots on areas applied - your skin reacts similarly with above when exposed to sunlight 2. Avoid applying on wounded, irritated, troubled areas 3. After the use - keep the cap closed - keep it out of children's reach - keep it away from expose to sunlight, high and low temperatures

DESCRIPTION

DESCRIPTION SECTION

INSTRUCTIONS: Layering Cushion CC covers face moisture as if it has done treatment. 3CE Tinted Moisture Cushion CC creates a moisture layer with a hydrating complex for dewy radiance.

Directions: Take a small amount with the Ruby Cell Puff and spread evenly over face. Please make sure to close the lid after use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60764-129-022020-01-31C16284748780-19d75b9d1-118e-f424-e053-dadaa90a57ce670674cb-c00e-491d-af0e-7f86abd40252

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60764-129-013CE Tinted moisture cushion CC 00112 g in 1 CONTAINERPOWDER121
60764-129-023CE Tinted moisture cushion CC 0012 in 1 CARTONPOWDER21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60764-1293CE TINTED MOISTURE CUSHION CC 001 (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) POWDER [NANDA CO., LTD]1Legacy NDC, 2 package rows20161017_670674cb-c00e-491d-af0e-7f86abd40252.zip

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
60764-12960764-129-01, 60764-129-02

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
445175f7-b886-473d-b5b4-1b3ff3fddb75670674cb-c00e-491d-af0e-7f86abd402522016-10-17WarningsExact identifier
spl id: 445175f7-b886-473d-b5b4-1b3ff3fddb75
spl set id: 670674cb-c00e-491d-af0e-7f86abd40252

Reported adverse events (FAERS/openFDA)#

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