FDA.reportPublic FDA data

GZE Brightenng Exfoliating Gel

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:38:49

Label at a glance#

ProductGZE Brightenng Exfoliating Gel
Active ingredientALLANTOIN, NIACINAMIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin

Niacinamide

INACTIVE INGREDIENT SECTION

Aqua

Butylene Glycol

Glycerin

Carbomer

Trehalose

Hydrolyzed Collagen

Aloe Barbadensis Leaf Extract

Hamamelis Virginiana (Witch Hazel) Extract

Centella Asiatica Extract

Phenoxyethanol

Ethylhexylglycerin

PEG-40 Hydrogenated Castor Oil

Fragrance

INDICATIONS & USAGE SECTION


After cleansing face, take appropriateproducts
smear on the face. Along the skin texture and gently massagein circular
motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

OTC - PURPOSE SECTION

Exfoliating.

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

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

DOSAGE & ADMINISTRATION SECTION


After cleansing face, take appropriateproducts
smear on the face. Along the skin texture and gently massagein circular
motions for 1-2 minutes, until thedead skin off the dirt.The rinse with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-037-01GZE Brightenng Exfoliating Gel50 g in 1 TUBEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-037GZE BRIGHTENNG EXFOLIATING GEL (ALLANTOIN 0.5% NIACINAMIDE 5%) GEL [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241124_2763d6e8-e2be-a406-e063-6394a90a6617.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
74458-03774458-037-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
HUMAN TYPE I COLLAGENPT3TGI7OIPIACT
NIACINAMIDE25X51I8RD4ACTIB
ALOE BARBADENSIS LEAF EXTRACTZY81Z83H0XIACT
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACTT07U1161SVIACT
GLYCERINPDC6A3C0OXIACT
TREHALOSEB8WCK70T7IIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PEG-40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
AQUA059QF0KO0RIACT
CARBOMER0A5MM307FCIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT

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
2763d6e8-e2bf-a406-e063-6394a90a66172763d6e8-e2be-a406-e063-6394a90a66172024-11-20WarningsExact identifier
spl id: 2763d6e8-e2bf-a406-e063-6394a90a6617
spl set id: 2763d6e8-e2be-a406-e063-6394a90a6617

Reported adverse events (FAERS/openFDA)#

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