FDA.reportPublic FDA data

GZE MULTI-EFFECT WHITENING SUNSCREEN

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:25:06

Label at a glance#

ProductGZE MULTI-EFFECT WHITENING SUNSCREEN
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide

Zinc Oxide

Niacinamide

INACTIVE INGREDIENT SECTION

Aqua

Cannabis Sativa Leaf Extract

Ascorbic Acid

Propylene Glycol

Glycerin

Trehalose

Allantoin

Sodium Hyaluronate

OTC - PURPOSE SECTION

Whiten and protect against the sun

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sun exposure.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabelStop use and ask a doctor if rash occurs.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-026-01GZE MULTI-EFFECT WHITENING SUNSCREEN60 g in 1 BOTTLE, PLASTICCREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-026GZE MULTI-EFFECT WHITENING SUNSCREEN (TITANIUM DIOXIDE 10% ZINC OXIDE 10%) CREAM [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241016_246da753-502b-b018-e063-6394a90a0f92.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-02674458-026-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CANNABIS SATIVA LEAFA718Z7DA1KIACT
NIACINAMIDE25X51I8RD4IACT
GLYCERINPDC6A3C0OXIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
ALLANTOIN344S277G0ZIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
TREHALOSEB8WCK70T7IIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
246da753-502c-b018-e063-6394a90a0f92246da753-502b-b018-e063-6394a90a0f922024-10-14WarningsExact identifier
spl id: 246da753-502c-b018-e063-6394a90a0f92
spl set id: 246da753-502b-b018-e063-6394a90a0f92

Reported adverse events (FAERS/openFDA)#

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