GZE UNDERARM SCRUB

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-11-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:35:25

Label at a glance#

ProductGZE UNDERARM SCRUB
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol

INACTIVE INGREDIENT SECTION

Aqua

Mineral Oil

Aloe Barbadensis Leaf Extract

Juglans Regia (Walnut)Shell Powder

Polysorbate 60

Carbomer

Sodium Chloride

CI 19140

CI 42090

OTC - PURPOSE SECTION

Exfoliation.

INDICATIONS & USAGE SECTION

Wet your body and scoop out the scrub and apply to your underarms, rubbing in circular motions for 2-3 minutes and rinse off with water.

OTC - PURPOSE 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.

WARNINGS 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 body and scoop out the scrub and apply to your underarms, rubbing in circular motions for 2-3 minutes and rinse off with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-226-01GZE UNDERARM SCRUB100 g in 1 JARGRANULE1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-226GZE UNDERARM SCRUB (MENTHOL 1.45%) GRANULE [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241109_265e85e8-927d-3bc1-e063-6294a90a6636.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-22674458-226-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
265e85e8-927e-3bc1-e063-6294a90a6636265e85e8-927d-3bc1-e063-6294a90a66362024-11-07WarningsExact identifier
spl id: 265e85e8-927e-3bc1-e063-6294a90a6636
spl set id: 265e85e8-927d-3bc1-e063-6294a90a6636

Reported adverse events (FAERS/openFDA)#

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