FDA.reportPublic FDA data

GZE SELF TAN ERASER

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:53:13

Label at a glance#

ProductGZE SELF TAN ERASER
Active ingredientETHYLHEXYLGLYCERIN
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethylhexylglycerin.

INACTIVE INGREDIENT SECTION

Aqua , Glycerin, Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Kaolin

OTC - PURPOSE SECTION

Tanning Remover.

INDICATIONS & USAGE SECTION

Pump a generous amount of SELF TAN ERASER foam onto dry skin. Massage the foam in circular motions for a few minutes, focusing on areas with excess self-tanner. Leave the foam on for at least 5 minutes to allow it to works. Rinse off the foam with warm water

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

Pump a generous amount of SELF TAN ERASER foam onto dry skin. Massage the foam in circular motions for a few minutes, focusing on areas with excess self-tanner. Leave the foam on for at least 5 minutes to allow it to works. Rinse off the foam with warm water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-329GZE SELF TAN ERASER (ETHYLHEXYLGLYCERIN 0.5%) LIQUID [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20241009_23df7340-4214-e19c-e063-6294a90a7f8d.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
74458-32974458-329-01

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
SODIUM BICARBONATE8MDF5V39QOIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ETHYLHEXYLGLYCERIN147D247K3PACTIB
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
ALOE VERA LEAFZY81Z83H0XIACT
KAOLIN24H4NWX5COIACT

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
3b398424-a705-e06e-e063-6294a90a02d823df7340-4214-e19c-e063-6294a90a7f8d2025-07-31WarningsExact identifier
spl set id: 23df7340-4214-e19c-e063-6294a90a7f8d

Reported adverse events (FAERS/openFDA)#

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