FDA.reportPublic FDA data

GZE Watery Sun Gel

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd.
Effective date
2024-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:12:32

Label at a glance#

ProductGZE Watery Sun Gel
Active ingredientCENTELLA ASIATICA
Label structure10 sections

Indications and uses

Gently apply to face, neck, & arms as the last step of your skincareroutine

Label contents#

Full prescribing information#

Active ingredients

INACTIVE INGREDIENT SECTION

WATER
TOCOPHEROL
CENTELLAASIATICA WHOLE
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER

Purpose

OTC - PURPOSE SECTION

Moisturising.

Uses

INTENDED USE OF THE DEVICE

Gently apply to face, neck, & arms as the last step of your skincareroutine

WARNINGS

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

CETYLALCOHOL
SODIUM PALMITOYL PROLINE
XANTHAN GUM
PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
ETHYLHEXYLGLYCERIN
ECTOINE
DIMETHYLSILANOL HYALURONATE
CENTELLAASIATICA WHOLE
TOCOPHEROL
ADENOSINE
WATER
PROPANEDIOL
1.3-BETA-GLUCAN SYNTHASE COMPONENT FKS1

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
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83566-200-01GZE Watery Sun Gel50 g in 1 TUBEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-200GZE WATERY SUN GEL (CENTELLA ASIATICA) GEL [GUANGDONG AIMU BIOLOGICAL TECHNOLOGY CO., LTD.]11 package rows20240516_18771133-54aa-2fae-e063-6294a90a0e8d.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-20083566-200-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
CETYL ALCOHOL936JST6JCNIACT
PROPANEDIOL5965N8W85TIACT
1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS14FRY3LJG0VIACT
WATER059QF0KO0RIACT
ADENOSINEK72T3FS567IACT
CENTELLA ASIATICA7M867G6T1UACTIB
HYALURONIC ACIDS270N0TRQYIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM PALMITOYL PROLINE64L053FRFOIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
TOCOPHEROLR0ZB2556P8IACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
DIMETHYLSILANOL HYALURONATEZ853O1D4TEIACT
ECTOINE7GXZ3858RYIACT

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
18771133-54ab-2fae-e063-6294a90a0e8d18771133-54aa-2fae-e063-6294a90a0e8d2024-05-14WarningsExact identifier
spl id: 18771133-54ab-2fae-e063-6294a90a0e8d
spl set id: 18771133-54aa-2fae-e063-6294a90a0e8d

Reported adverse events (FAERS/openFDA)#

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