FACET IT PURE 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 22:41:49

Label at a glance#

ProductFACET IT PURE COLOR CONTROL 32800851
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure10 sections

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. Dispense an adeq...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE 4.0%
TITANIUM DIOXIDE 10.2%,
ZINC OXIDE 1.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

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.
Dispense an adequate amount at the last stage of
your skincare and apply evenly on the face.

To keep your face looking fresh, use with Face it Aura CC
Cream.

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•CYCLOPENTASILOXANE•CYCLOHEXASILOXANE•PHENYL
TRIMETHICONE•GLYCERIN•BUTYLENE GLYCOL DICAPRYLATE/
DICAPRATE•DIMETHICONE•BUTYLENE GLYCOL•PEG-8•
NIACINAMIDE•CETYL PEG/PPG-10/1 DIMETHICONE•PENTYLENE
GLYCOL•SODIUM CHLORIDE•DICAPRYLYL CARBONATE•
SORBITAN ISOSTEARATE•DISTEARDIMONIUM HECTORITE•
C30-45 ALKYLDIMETHYLSILYL POLYPROPYLSILSESQUIOXANE•
PHENOXYETHANOL•DIMETHICONE CROSSPOLYMER•
TRIETHOXYCAPRYLYLSILANE•ALUMINUM HYDROXIDE•STEARIC
ACID•ETHYLHEXYLGLYCERIN•ADENOSINE•DISODIUM EDTA•
VITIS VINIFERA (GRAPE) FRUIT EXTRACT•OENOTHERA BIENNIS
(EVENING PRIMROSE) OIL•ONSEN-SUI•SODIUM PCA•UREA•
POLYPERFLUOROMETHYLISOPROPYL ETHER•LONICERA
JAPONICA (HONEYSUCKLE) FLOWER EXTRACT•IMPERATA
CYLINDRICA ROOT EXTRACT•TREHALOSE•POLYQUATERNIUM-51•
CITRUS RETICULATA (TANGERINE) PEEL EXTRACT•
ACHYRANTHES FAURIEI ROOT EXTRACT•SODIUM
HYALURONATE•TRIACETIN•CAPRYLYL GLYCOL•1,2-HEXANEDIOL•
CARBOMER•METHYLPARABEN•POTASSIUM SORBATE•OXYGEN•
BUTYLPARABEN•ETHYLPARABEN•PROPYLPARABEN•
ISOBUTYLPARABEN•FRAGRANCE(PARFUM)•
MICA (CI 77019)•IRON OXIDES (CI 77491,
CI 77492, CI 77499)

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.

OTC - QUESTIONS SECTION

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

Distributed by:

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COLOR CONTROL

CC

CREAM

PURE CC

SUNSCREEN CREAM SPF30

02 NATURAL BEIGE

Image-label-32800851-revImage-label-32800851-rev

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-851-292020-01-31C16284748780-19d75b9d0-8767-f424-e053-dadaa90a57ce0813c3dd-9a24-174b-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-851-29FACET IT PURE COLOR CONTROL3280085140 mL in 1 TUBECREAM401
51523-851-29FACET IT PURE COLOR CONTROL328008511 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-851FACET IT PURE COLOR CONTROL 32800851 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150225_0813c3dd-9a24-174b-e054-00144ff8d46c.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
51523-85151523-851-29

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
0813c3dd-9a25-174b-e054-00144ff8d46c0813c3dd-9a24-174b-e054-00144ff8d46c2014-11-20WarningsExact identifier
spl id: 0813c3dd-9a25-174b-e054-00144ff8d46c
spl set id: 0813c3dd-9a24-174b-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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