FDA.reportPublic FDA data

3CE DUO COLOR FACE BLUSH RETRO DRIVE

Manufacturer
Nanda Co., Ltd | Cosmax, Inc.
Effective date
2016-10-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:47:20

Label at a glance#

Product3CE DUO COLOR FACE BLUSH RETRO DRIVE
Active ingredientTitanium Dioxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Titanium Dioxide 2.4%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Mica (CI 77019), Talc, Octyldodecyl Stearoyl Stearate, Phenyl Trimethicone, Magnesium Myristate, Nylon-12, Magnesium Stearate, Red 6 (CI 15850), Yellow 5 Lake (CI 19140), Polyethylene, Silica, Iron Oxides (CI 77492), Propanediol, Triethoxycaprylylsilane, Dimethicone, PTFE, Ethylhexyl Methoxycinnamate, Iron Oxides (CI 77491), Sodium Dehydroacetate, Caprylic/Capric Triglyceride, Methicone

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: Achieve a beautiful flush on your skin with this pigmented blush.

Directions: With a brush, dab on the center of both cheeks then follow with spreading out by dabbing around the face line

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60764-061-022020-01-31C16284748780-19d75b9d0-357d-f424-e053-dadaa90a57cea1356f98-d62a-4197-b82c-4b435e195093

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60764-061-013CE DUO COLOR FACE BLUSH RETRO DRIVE5 g in 1 CONTAINERPOWDER51
60764-061-023CE DUO COLOR FACE BLUSH RETRO DRIVE1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60764-0613CE DUO COLOR FACE BLUSH RETRO DRIVE (TITANIUM DIOXIDE) POWDER [NANDA CO., LTD]1Legacy NDC, 2 package rows20161004_a1356f98-d62a-4197-b82c-4b435e195093.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60764-06160764-061-01, 60764-061-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Titanium Dioxide15FIX9V2JPACTIB
MicaV8A1AW0880IACT
Talc7SEV7J4R1UIACT

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
b8c9cea5-61eb-4f54-a014-5af0882c65c5a1356f98-d62a-4197-b82c-4b435e1950932016-10-04WarningsExact identifier
spl id: b8c9cea5-61eb-4f54-a014-5af0882c65c5
spl set id: a1356f98-d62a-4197-b82c-4b435e195093

Reported adverse events (FAERS/openFDA)#

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