FACE IT AURA COLOR CONTROL

Manufacturer
THEFACESHOP CO., LTD. | THEFACESHOP NORTH AMERICA, INC.
Effective date
2014-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:41:50

Label at a glance#

ProductFACE IT AURA COLOR CONTROL 32800660
Active ingredientZINC OXIDE, OCTINOXATE, TITANIUM DIOXIDE
Label structure10 sections

Indications and uses

Helps prevent sunburn

Dosage and administration

Apply generously and evenly 15 minutes before sun exposure. Children under 6 months of age: Ask a doctor Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging. Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE............ 4.0%
TITANIUM DIOXIDE 11.5%
ZINC OXIDE............... 1.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen
Sunscreen

Uses

OTC - PURPOSE SECTION

Helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison
Control Center right away.

Directions

OTC - WHEN USING SECTION

Apply generously and evenly 15 minutes before sun exposure.
Children under 6 months of age: Ask a doctor
Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early
skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.
Reapply at least every 2 hours.

Use a water-resistant sunscreen if swimming or sweating.

Other Information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun.
May stain or damage some fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

WATER•DIPHENYLSILOXY PHENYL TRIMETHICONE•CYCLOPENTASILOXANE•GLYCERIN•CYCLOHEXASILOXANE•
BUTYLENE GLYCOL•BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE•NIACINAMIDE•CETYL PEG/PPG-10/1 DIMETHICONE•
MALTITOL•SORBITAN ISOSTEARATE•OCTYLDODECANOL•CAPRYLYL METHICONE•TRIMETHYLSILOXYSILICATE•
TRIBEHENIN•PENTYLENE GLYCOL•PEG-10 DIMETHICONE•HEXYL LAURATE•DISTEARDIMONIUM HECTORITE•MAGNESIUM
SULFATE•DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER•METHYL METHACRYLATE CROSSPOLYMER•DIPHENYL
DIMETHICONE•VP/HEXADECENE COPOLYMER•PHENOXYETHANOL•TRIETHOXYCAPRYLYLSILANE•CERESIN•
ALUMINUM HYDROXIDE•STEARIC ACID•ETHYLHEXYLGLYCERIN•ADENOSINE•DIMETHICONE•
DISODIUM EDTA•SODIUM PCA•SODIUM HYALURONATE•UREA•TREHALOSE•POLYQUATERNIUM-51•CITRUS RETICULATA
(TANGERINE) PEEL EXTRACT•ACHYRANTHES FAURIEI ROOT EXTRACT•ACTINIDIA POLYGAMA FRUIT EXTRACT•
IMPERATA CYLINDRICA ROOT EXTRACT•POLYPERFLUOROMETHYLISOPROPYL ETHER•OXYGEN•
PEG-8•CARBOMER•METHYLPARABEN•POTASSIUM SORBATE•BUTYLPARABEN•ETHYLPARABEN•
PROPYLPARABEN•ISOBUTYLPARABEN•FRAGRANCE (PARFUM)•IRON OXIDES (CI 77491, CI 77492,
CI 77499)•MICA (CI 77019)

Questions

OTC - QUESTIONS SECTION

Questions or comments? Call 1 (866) 638-8417

Distributed by:

SPL UNCLASSIFIED SECTION

Distributed by:

THEFACESHOP NORTH AMERICA, INC. / Santa Fe Springs, CA 90670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COLOR CONTROL CC CREAM
AURA COLOR CONTROL
SUNSCREEN CREAM (REFILL)
SPF30
02 NATURAL BEIGE

FACE IT CC CREAM is a color-controlling cream that brightens your complexion
and keeps your morning makeup intact without any darkening.

FACE it

Image-label-32800660-revImage-label-32800660-rev

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-660-172020-01-31C16284748780-19d75b9d0-8773-f424-e053-dadaa90a57ce080ff250-52b7-0992-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-660-17FACE IT AURA COLOR CONTROL328006601 in 1 CARTONCREAM11
51523-660-17FACE IT AURA COLOR CONTROL3280066020 g in 1 CONTAINERCREAM201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-660FACE IT AURA COLOR CONTROL 32800660 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150226_080ff250-52b7-0992-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51523-66051523-660-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
080ff250-52b8-0992-e054-00144ff88e88080ff250-52b7-0992-e054-00144ff88e882014-11-20WarningsExact identifier
spl id: 080ff250-52b8-0992-e054-00144ff88e88
spl set id: 080ff250-52b7-0992-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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