FACE IT AQUA TINTED

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 22:41:45

Label at a glance#

ProductFACE IT AQUA TINTED 32800421

Active ingredientOCTINOXATE

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. Apply after skin...

Contacts and useful links#

PhoneLabel contact1 (866) 638-8417

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE • • • • • • • • • 5.0%

Purpose

OTC - PURPOSE SECTION

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.

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.

Apply after skincare products. Blend evenly with

fingertips and gently pat into skin.

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•TITANIUM DIOXIDE•CYCLOMENTHICONE•

BUTYLENE GLYCOL•HEXYL LAURATE•GLYCERIN•

SD ALCOHOL 40-B•BIOSACCHARIDE GUM-1•

PORTULACA OLERACEA EXTRACT•

HYDROXYETHYL ACRYLATE/SODIUM

ACRYLOYLDIMETHYL TAURATE COPOLYMER•

C9-15 FLUOROALCOHOL PHOSPHATE•SQUALANE•

PHENOXYETHANOL•TALC•METHYLPARABEN•

ALUMINUM HYDROXIDE, ETHYLPARABEN•

POLYSORBATE 60•BUTYLPFENYL

METHYLPROPIONAL•HYDROXYISOHEXYL

3-CYCLOHEXENE CARBOXALDEHYDE•LINALOOL•

BUTYLPFENYL METHYLPROPIONAL•

CITRONELLOL•LIMONENE•SEA WATER•

PONCIRUS TRIFOLIATA FRUIT EXTRACT•

TRIETHOXYCAPRYLYLSILANE•

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

AQUA TINTED

BB SUNSCREEN CREAM SPF20

02 NATURAL BEIGE

With a 70 % MOISTURE CONTENT, including

DEEP SEA WATER, a light application provides

a sense of coolness and freshness the moment it touches the skin.

Image-label-32800421-rev

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51523-421-11	2020-01-31	C162847	48780-1	9d75b9d0-2c9b-f424-e053-dadaa90a57ce	FACE IT AQUA TINTED 32800421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51523-421-11	FACE IT AQUA TINTED32800421	1 in 1 CARTON	CREAM	1		1
51523-421-11	FACE IT AQUA TINTED32800421	40 mL in 1 TUBE	CREAM	40		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51523-421	FACE IT AQUA TINTED 32800421 (OCTINOXATE) CREAM [THEFACESHOP CO., LTD.]	1	Legacy NDC, 2 package rows	20150223_08105130-2d59-72c2-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

FACE IT AQUA TINTED 32800421
octinoxate
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51523-421	51523-421-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
WATER	059QF0KO0R	IACT

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
08105130-2d5a-72c2-e054-00144ff8d46c			08105130-2d59-72c2-e054-00144ff8d46c	2014-11-20	Warnings	Exact identifier spl id: 08105130-2d5a-72c2-e054-00144ff8d46c spl set id: 08105130-2d59-72c2-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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