FACE IT POWER PERFECTION

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 22:41:34

Label at a glance#

ProductFACE IT POWER PERFECTION 32800311
Active ingredientOCTINOXATE, ZINC OXIDE, TITANIUM DIOXIDE
Label structure9 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. After basic skin...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE • • • • • • • • • • • 5.0%
TITANIUM DIOXIDE • • • • • • • • 10.0%
ZINC OXIDE • • • • • • • • • • • 2.9%

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.
After basic skincare, dispense an adequate amount
and apply evenly to the skin. Then, pat lightly with the
palms for full absorption.

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

CYCLOPENTASILOXANE•PHENYL TRIMETHICONE•
CYCLOHEXASILOXANE•BUTYLENE GLYCOL•
ISODODECANE•CETYLEG/PPG-10/1 DIMETHICONE•
NIACINAMIDE•METHYLPROPANEDIOL•BUTYLENE
GLYCOL•DICAPRYLATE/DICAPRATE•POLYGLYCERYL-4
ISOSTEARATE•SODIUM CHLORIDE•METHYL
METHACRYLATE CROSSPOLYMER•HYDROGENATED
POLYISOBUTENE•DISTEARDIMONIUM HECTORITE•
SORBITAN ISOSTEARATE•OZOKERITE•DIMETHICONE•
HEXYL LAURATE•DIMETHICONE/VINYL DIMETHICONE
CROSSPOLYMER•HYDROGENATED POLY(C6-14 OLEFIN)•
CAPRYLIC/CAPRIC GLYCERIDES•ETHYLHEXYLGLYCERIN•
ALUMINUM HYDROXIDE•BEESWAX•STEARIC ACID•
FRAGRANCE(PARFUM)•TRIETHOXYCAPRYLYLSILANE•
PROPYLENE CARBONATE•DISODIUM EDTA•PRUNUS
AMYGDALUS DULCIS (SWEET ALMOND) OIL•RASPBERRY
SEED OIL/TOCOPHERYL SUCCINATE AMINOPROPANEDIOL
ESTERS•ADENOSINE•PORTULACA OLERACEA EXTRACT•
XANTHAN GUM•SODIUM HYALURONATE•PLUKENETIA
VOLUBILIS SEED OIL•ALUMINA•RETINOL•LINOLEIC ACID•
CERAMIDE 3•TOCOPHEROL•ASCORBIC ACID•HYDROLYZED
EXTENSIN•GLYCERIN•SCHINUS TEREBINTHIFOLIUS SEED
EXTRACT•PHENOXYETHANOL•GYNOSTEMMA
PENTAPHYLLUM LEAF/STEM EXTRACT•CALCIUM
ALUMINUM BOROSILICATE•BETA-GLUCAN•
METHYLPARABEN•BUTYLPARABEN•ETHYLPARABEN•
ISOBUTYLPARABEN•PROPYLPARABEN•
IRON OXIDES (CI 77491, CI 77492, CI 77499)

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

FACE IT POWER PERFECTION BB CREAM 01 LIGHT BEIGE

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51523-311-042020-01-31C16284748780-19d75b9d0-b21e-f424-e053-dadaa90a57ceFACE IT POWER PERFECTION 32800311

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-311-04FACE IT POWER PERFECTION3280031140 g in 1 TUBECREAM401
51523-311-04FACE IT POWER PERFECTION328003111 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-311FACE IT POWER PERFECTION 32800311 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150202_07d5e76a-da75-04b4-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
ALUMINUM OXIDEINACTIVE INGREDIENTLMI26O69331

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
51523-31151523-311-04

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

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALUMINUM OXIDEALUMINUM OXIDELMI26O6933SPONGE / TOPICALNAExact identifier — unii candidate
2 equally ranked IID candidates
ALUMINUM OXIDEALUMINUM OXIDELMI26O6933TABLET / ORALNAExact identifier — unii candidate
2 equally ranked IID candidates

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
07d5e76a-da76-04b4-e054-00144ff88e8807d5e76a-da75-04b4-e054-00144ff88e882014-11-20WarningsExact identifier
spl id: 07d5e76a-da76-04b4-e054-00144ff88e88
spl set id: 07d5e76a-da75-04b4-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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