shu uemura UV under base mousse

Manufacturer: Cosmelor Ltd
Effective date: 2010-03-03
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 01:54:19

Label at a glance#

Productshu uemura UV under base mousse SPF 30 sunscreen

Active ingredientOctinoxate, Octisalate, Octocrylene, Titanium Dioxide

Label structure4 sections

Indications and uses

USES: Helps prevent sunburn. Higher SPF gives more sunburn protection. DIRECTIONS: For sunscreen benefits, apply evenly before sun exposure. Use as a makeup base before foundation or alone for even skin tone. Shake well before use. Dispense product into palm of hand with nozzle facing upwards. Please store at room temperature.

Dosage and administration

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS

OCTINOXATE 7.12%

OCTISALATE 4.7%

OCTOCRYLENE 2.85%

TITANIUM DIOXIDE 4.75%

USES: DIRECTIONS:

INDICATIONS & USAGE SECTION

USES: Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS: For sunscreen benefits, apply evenly before sun exposure. Use as a makeup base before foundation or alone for even skin tone. Shake well before use. Dispense product into palm of hand with nozzle facing upwards. Please store at room temperature.

WARNINGS:

WARNINGS SECTION

WARNINGS: FOR EXTERNAL USE ONLY, NOT TO BE SWALLOWED. AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. DISCONTINUE USE IF SIGNS OF IRRITATION OR RASH APPEAR. IF IRRITATION OR RASH PERSISTS, CONSULT A DOCTOR. KEEP OUT OF REACH OF CHILDREN. FLAMMABLE. AVOID FIRE, FLAME, HEAT AND SMOKING DURING APPLICATION. CONTENTS UNDER PRESSURE. DO NOT PUNCTURE OR INCINERATE. DO NOT STORE AT TEMPERATURES ABOVE 120 F. USE ONLY AS DIRECTED.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of carton labelEnter section text here

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68570-744-01	2025-01-04	C162847	48780-1	956f9ecf-dbff-621f-e053-dbdaa90a74ad	Drug Facts
68570-744-01	2019-10-21	C162847	48780-1	956f9ecf-dbff-621f-e053-dbdaa90a74ad	Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Octinoxate	ACTIVE INGREDIENT	4Y5P7MUD51	2
Octisalate	ACTIVE INGREDIENT	4X49Y0596W	2
Octocrylene	ACTIVE INGREDIENT	5A68WGF6WM	2
Titanium Dioxide	ACTIVE INGREDIENT	15FIX9V2JP	2
Octinoxate	ACTIVE MOIETY	4Y5P7MUD51	2
Octisalate	ACTIVE MOIETY	4X49Y0596W	2
Octocrylene	ACTIVE MOIETY	5A68WGF6WM	2
Titanium Dioxide	ACTIVE MOIETY	15FIX9V2JP	2

Products#

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

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

shu uemura UV under base mousse SPF 30 sunscreen
Octinoxate Octisalate Octocrylene Titanium Dioxide
Octinoxate
Octisalate
Octocrylene
Titanium Dioxide

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68570-744	68570-744-01

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
Octisalate	4X49Y0596W	ACTIB
Octocrylene	5A68WGF6WM	ACTIB
Titanium Dioxide	15FIX9V2JP	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
0d9b508d-64d6-4c69-ac52-2829586e588f			eedac138-d1f2-4a66-9748-0b1453caf6a1	2025-01-02	Warnings	Exact identifier spl set id: eedac138-d1f2-4a66-9748-0b1453caf6a1

Reported adverse events (FAERS/openFDA)#

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