GZE HONEY MILK HAND WAX

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:36:27

Label at a glance#

ProductGZE HONEY MILK HAND WAX
Active ingredientHONEY EXTRACT, BEESWAX
Label structure11 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

Water

Polyvinyl Alcohol

Parfum

Sodium Polyacrylate

Ethylhexyl Stearate

Diazolidinyl Urea

Trideceth-6

1,2-Butanediol

Glycerin

CI 19140

OTC - ACTIVE INGREDIENT SECTION

Beewax

Honey Extract

OTC - PURPOSE SECTION

Exfoliation.

INDICATIONS & USAGE SECTION

Apply hand wax and spread a uniform layer of about 1 mm thick with a spoon.Wait 15-20 minutes, then remove the hardened film from your hands.

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

Apply hand wax and spread a uniform layer of about 1 mm thick with a spoon.Wait 15-20 minutes, then remove the hardened film from your hands.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74458-058-01GZE HONEY MILK HAND WAX120 g in 1 JARPASTE1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-058GZE HONEY MILK HAND WAX (BEESWAX 5% HONEY EXTRACT 5%) PASTE [GUANGZHOU YILONG COSMETICS CO., LTD]11 package rows20241110_2673485f-2c4e-e882-e063-6394a90a5d4e.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-05874458-058-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
2673485f-2c4f-e882-e063-6394a90a5d4e2673485f-2c4e-e882-e063-6394a90a5d4e2024-11-08WarningsExact identifier
spl id: 2673485f-2c4f-e882-e063-6394a90a5d4e
spl set id: 2673485f-2c4e-e882-e063-6394a90a5d4e

Reported adverse events (FAERS/openFDA)#

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