FACE IT

Manufacturer: THEFACESHOP NORTH AMERICA, INC. | THEFACESHOP CO., LTD.
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#

ProductFACE IT 32800285

Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE

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 Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating.

Contacts and useful links#

PhoneLabel contact1 (866) 638-8417

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE.......... .5.5%

TITANIUM DIOXIDE .5.7%

ZINC OXIDE ............. 3.0%

Purpose

OTC - PURPOSE SECTION

Sunscreen
Sunscreen
Sunscreen

Uses

OTC - WHEN USING 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.

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.

Directions

OTC - WHEN USING SECTION

Apply generously and evenly 15 minutes before sun exposure.

Children under 6 months of age: Ask a doctor

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•CYCLOPENTASILOXANE•MICA•

TRIETHOXYCAPRYLYLSILANE•DIPROPYLENE

GLYCOL•PROPYLENE GLYCOL•PHENYL

TRIMETHICONE•DIMETHICONE CROSSPOLYMER•

LAURYL PEG-8 DIMETHICONE•SILICA•METHICONE•

DIMETHICONE•DIMETHICONE/VINYL DIMETHICONE

CROSSPOLYMER•DISTEARDIMONIUM HECTORITE•

POLYGLYCERYL-6 POLYRICINOLEATE•MANNAN•

SODIUM CHLORIDE•LECITHIN•PROPYLENE

CARBONATE•CITRUS PARADISI(GRAPEFRUIT)

FRUIT EXTRACT•METHYLPARABEN•DISODIUM

EDTA•AMETHYST POWDER•RUBY POWDER•

QUARTZ•NEPHRITE POWDER•SAPPHIRE POWDER•

TOURMALINE•BUTYLENE GLYCOL•CENTELLA

ASIATICA EXTRACT•CAMELLIA SINENSIS LEAF

EXTRACT•HEDERA HELIX (IVY) LEAF/STEM

EXTRACT•ANTHEMIS NOBILIS FLOWER EXTRACT•

FRAGRANCE•IRON OXIDES

(CI 77491, CI 77492, CI 77499)

OTC - QUESTIONS SECTION

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

SPL UNCLASSIFIED SECTION

Distributed by:

THEFACESHOP NORTH AMERICA, INC.

Santa Fe Springs, CA 90670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SHIMMERING BB CREAM

SUNSCREEN CREAM SPF20

This BB cream contains "Crystal Modeling Powder" which offers a

radian, luminous complexion and "Jewel Repair Complex" which is

a skin repair complex that keeps skin healthy.

Image-label-32800285-rev

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51523-285-03	2020-01-31	C162847	48780-1	9d75b9d0-5ad3-f424-e053-dadaa90a57ce	07d4e9a6-8731-5c4f-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51523-285-03	FACE IT32800285	40 mL in 1 TUBE	CREAM	40		1
51523-285-03	FACE IT32800285	1 in 1 CARTON	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51523-285	FACE IT 32800285 (OCTINOXATE, TITANIUM OXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP NORTH AMERICA, INC.]	1	Legacy NDC, 2 package rows	20150225_07d4e9a6-8731-5c4f-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
TITANIUM DIOXIDE	ACTIVE INGREDIENT	15FIX9V2JP	1
ZINC OXIDE	ACTIVE INGREDIENT	SOI2LOH54Z	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
TITANIUM DIOXIDE	ACTIVE MOIETY	15FIX9V2JP	1
ZINC OXIDE	ACTIVE MOIETY	SOI2LOH54Z	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

FACE IT 32800285
octinoxate, titanium oxide and zinc oxide cream
OCTINOXATE
WATER
TITANIUM DIOXIDE
ZINC OXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51523-285	51523-285-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
WATER	059QF0KO0R	IACT
TITANIUM DIOXIDE	15FIX9V2JP	ACTIB
ZINC OXIDE	SOI2LOH54Z	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
07d4e9a6-8732-5c4f-e054-00144ff88e88			07d4e9a6-8731-5c4f-e054-00144ff88e88	2014-11-20	Warnings	Exact identifier spl id: 07d4e9a6-8732-5c4f-e054-00144ff88e88 spl set id: 07d4e9a6-8731-5c4f-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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