GZE Glutathione BrighteningSoap

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:31:04

Label at a glance#

ProductGZE Glutathione BrighteningSoap
Active ingredientGLUTATHIONE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Glutathione

INACTIVE INGREDIENT SECTION

Sodium Palmitate

Sodium Stearate

Glycerin

Titanium Dioxide

Fragrance

OTC - PURPOSE SECTION

Brightens skin tone.

INDICATIONS & USAGE SECTION

Wet your hands and the soap bar with water. Iather the soap in your hands until it creates a rich foam. Gently massage the foam onto your damp skin, focusing on areas you want to lighten. Leave the soap on your skin for a few minutes before rinsing off with 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

Wet your hands and the soap bar with water. Iather the soap in your hands until it creates a rich foam. Gently massage the foam onto your damp skin, focusing on areas you want to lighten. Leave the soap on your skin for a few minutes before rinsing off with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-331-01GZE Glutathione BrighteningSoap100 g in 1 BAGSOAP1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-331GZE GLUTATHIONE BRIGHTENINGSOAP (GLUTATHIONE 2%) SOAP [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241030_2594dbf4-f07d-4bae-e063-6294a90ad414.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-33174458-331-01

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
2594dbf4-f07e-4bae-e063-6294a90ad4142594dbf4-f07d-4bae-e063-6294a90ad4142024-10-28WarningsExact identifier
spl id: 2594dbf4-f07e-4bae-e063-6294a90ad414
spl set id: 2594dbf4-f07d-4bae-e063-6294a90ad414

Reported adverse events (FAERS/openFDA)#

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