FDA.reportPublic FDA data

GZE Tinted Sunscreen

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:26:59

Label at a glance#

ProductGZE Tinted Sunscreen
Active ingredientZINC OXIDE
Label structure11 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Water

Resveratrol

Epicatechin

Ascorbic Acid Polypeptide

Adenosine

Trihydroxystearin

Pomegranate Fruit Peel Extract Octenylsuccinate

Haematococcus Pluvialis Extract

Hydrolyzed Corn Starch

Polysorbate 80

Hexanediol

Sodium Arganate

Methyl Hexyl Cyclopentanone Carboxylate

Bismuth Iron Oxide

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide

OTC - PURPOSE SECTION

Sunscreen.

INDICATIONS & USAGE SECTION

Apply full body sunscreen ahead of time, avoiding the eye area, for the first fifteen minutes of exposure to the sun.

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

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 full body sunscreen ahead of time, avoiding the eye area, for the first fifteen minutes of exposure to the sun.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-009-01GZE Tinted Sunscreen40 mL in 1 TUBELOTION401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-009GZE TINTED SUNSCREEN (ZINC OXIDE 15%) LOTION [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241019_24bdcbc6-8644-a3ab-e063-6394a90a831e.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-00974458-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASCORBIC ACIDPQ6CK8PD0RIACT
HEXANEDIOLZIA319275IIACT
WATER059QF0KO0RIACT
RESVERATROLQ369O8926LIACT
EPICATECHIN34PHS7TU43IACT
HAEMATOCOCCUS PLUVIALIS31T0FF0472IACT
STARCH, CORNO8232NY3SJIACT
ZINC OXIDESOI2LOH54ZACTIB
ADENOSINEK72T3FS567IACT
TRIHYDROXYSTEARIN06YD7896S3IACT
POLYSORBATE 806OZP39ZG8HIACT
POMEGRANATE56687D1Z4DIACT
METHYL HEXYL CYCLOPENTANONE CARBOXYLATE2JE1P6GLJFIACT

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
24bdd656-3818-a4ac-e063-6394a90aa91524bdcbc6-8644-a3ab-e063-6394a90a831e2024-10-18WarningsExact identifier
spl id: 24bdd656-3818-a4ac-e063-6394a90aa915
spl set id: 24bdcbc6-8644-a3ab-e063-6394a90a831e

Reported adverse events (FAERS/openFDA)#

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