shu uemura face architect

Manufacturer
Cosmelor Ltd
Effective date
2010-06-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 01:53:01

Label at a glance#

Productshu uemura face architect glow enhancing foundation SPF 26
Active ingredientOctinoxate, Zinc Oxide
Label structure4 sections

Indications and uses

USES: Helps prevent sunburn. Higher SPF give more sunburn protection. DIRECTIONS: For sunscreen benefits, apply evenly before sun exposure.

Dosage and administration

USES: Helps prevent sunburn. Higher SPF give more sunburn protection. DIRECTIONS: For sunscreen benefits, apply evenly before sun exposure.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE 5.74%, ZINC OXIDE 3.41%

USES: DIRECTIONS:

INDICATIONS & USAGE SECTION

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

DIRECTIONS: For sunscreen benefits, apply evenly before sun exposure.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of carton label
image of carton label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68570-812-012025-01-04C16284748780-1956f9ecf-cefd-621f-e053-dbdaa90a74adDrug Facts
68570-812-012019-10-21C16284748780-1956f9ecf-cefd-621f-e053-dbdaa90a74adDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OctinoxateACTIVE INGREDIENT4Y5P7MUD514
Zinc OxideACTIVE INGREDIENTSOI2LOH54Z4
OctinoxateACTIVE MOIETY4Y5P7MUD514
Zinc OxideACTIVE MOIETYSOI2LOH54Z4

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68570-81268570-812-01

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
NameUNIIKind
Octinoxate4Y5P7MUD51ACTIB
Zinc OxideSOI2LOH54ZACTIB

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
a0a105e6-cbeb-43dc-8107-e6deb0be1c41425714c0-e125-4f83-ac81-2f75d5c35c342025-01-02WarningsExact identifier
spl set id: 425714c0-e125-4f83-ac81-2f75d5c35c34

Reported adverse events (FAERS/openFDA)#

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