FDA.reportPublic FDA data

GZE Watery Sun Gel

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:49:06

Label at a glance#

ProductGZE Watery Sun Gel
Active ingredientHYALURONIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hyaluronic Acid 0.2%

OTC - PURPOSE SECTION

Moisturizing

INDICATIONS & USAGE SECTION


Gently apply to face, neck,
& arms as the last step of your skincare routine.

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


Gently apply to face, neck and arms as the last step of your skincare routine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-200GZE WATERY SUN GEL (HYALURONIC ACID 0.2%) GEL [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20241121_273f11f7-891d-5ece-e063-6394a90a80af.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-20074458-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYACTIB
WATER059QF0KO0RIACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
SODIUM HYALURONATEYSE9PPT4THIACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
TOCOPHEROLR0ZB2556P8IACT
GLYCERINPDC6A3C0OXIACT

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
3b391f4f-bd26-715a-e063-6294a90a95e4273f11f7-891d-5ece-e063-6394a90a80af2025-07-31WarningsExact identifier
spl set id: 273f11f7-891d-5ece-e063-6394a90a80af

Reported adverse events (FAERS/openFDA)#

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