GZE Aloe Vera Gel

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:57:05

Label at a glance#

ProductGZE Aloe Vera Gel
Active ingredientCITRIC ACID, 1-STEARYL ESTER, CENTELLA ASIATICA
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Centella asiatica

Citric Acid

INACTIVE INGREDIENT SECTION

Organic Aloe Vera

Potassium Sorbate

Ascorbic Acid

And Xanthan

OTC - PURPOSE SECTION

Skin care.

INDICATIONS & USAGE SECTION

Apply a thin layer of Aloe Vera Gel to affected area as needed.

WARNINGS SECTION

1. 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 a thin layer of Aloe Vera Gel to affected area as needed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-022GZE ALOE VERA GEL (CENTELLA ASIATICA,CITRIC ACID) GEL [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20240808_1eec0b65-4fe7-bb35-e063-6294a90abb45.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
83566-02283566-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
39f5db1b-75ba-b27f-e063-6294a90af5c71eec0b65-4fe7-bb35-e063-6294a90abb452025-07-15WarningsExact identifier
spl set id: 1eec0b65-4fe7-bb35-e063-6294a90abb45

Reported adverse events (FAERS/openFDA)#

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