FDA.reportPublic FDA data

GZE Scar Gel

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:29:00

Label at a glance#

ProductGZE Scar Gel
Active ingredientALLANTOIN
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%

INACTIVE INGREDIENT SECTION

Water (purified)

PEG 200

Alcohol

Xanthan Gum

Lecithin

Methylparaben

Sorbic Acid

Panthenol

Sodium Hyaluronate

Fragrance

INDICATIONS & USAGE SECTION

Apply evenly and gently rub into the scar once a day for 8 weeks on new sars, and once a day for 3-6 months on existing scars.Apply Scar Gel as soon as your wound has closed.

OTC - PURPOSE SECTION

Skin care for scar.

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 - 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 evenly and gently rub into the scar once a day for 8 weeks on new sars, and once a day for 3-6 months on existing scars.Apply Scar Gel as soon as your wound has closed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1442087allantoin 0.5 % Topical GelPSN1
1442087allantoin 0.005 MG/MG Topical GelSCD1
1442087allantoin 0.5 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-027-01GZE Scar Gel30 g in 1 TUBEGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-027GZE SCAR GEL (ALLANTOIN 0.5%) GEL [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241025_25346f77-6917-e665-e063-6294a90aa88d.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-02774458-027-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
LECITHIN, SOYBEAN1DI56QDM62IACT
SODIUM HYALURONATEYSE9PPT4THIACT
ALCOHOL3K9958V90MIACT
PANTHENOLWV9CM0O67ZIACT
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT
ALLIUM CEPA (ONION) BULB EXTRACT492225Q21HIACT
SORBIC ACIDX045WJ989BIACT
POLYETHYLENE GLYCOL 200R95B8J264JIACT
XANTHAN GUMTTV12P4NEEIACT
METHYLPARABENA2I8C7HI9TIACT
FRAGRANCE 135765EM498GW35IACT

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
25346f77-6918-e665-e063-6294a90aa88d25346f77-6917-e665-e063-6294a90aa88d2024-10-24WarningsExact identifier
spl id: 25346f77-6918-e665-e063-6294a90aa88d
spl set id: 25346f77-6917-e665-e063-6294a90aa88d

Reported adverse events (FAERS/openFDA)#

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