FDA.reportPublic FDA data

GZE black hair DyeShampoo

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-06-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:00:35

Label at a glance#

ProductGZE black hair DyeShampoo
Active ingredientRESORCINOL, STEARAMIDOETHYL ETHANOLAMINE MONOPHOSPHATE, THUJA OCCIDENTALIS LEAF, MANCHURIAN WALNUT SHELL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

RESORCINOL
MANCHURIAN WALNUT SHELL
THUJA OCCIDENTALIS LEAF
STEARAMIDOETHYL ETHANOLAMINE MONOPHOSPHATE

INACTIVE INGREDIENT SECTION

ASCORBIC ACID
ACRYLATES CROSSPOLYMER-6
CETEARETH-25
WATER
GLYCERYL STEARATE SE
ETIDRONIC ACID

OTC - PURPOSE SECTION

Hair Dye.

INDICATIONS & USAGE SECTION

Skin test before using; Keep hair dry, wear the gloves; Apply on wet hair and avoid touching your for ehead, wash with water after 20 minutes.

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

Skin test before using; Keep hair dry, wear the gloves; Apply on wet hair and avoid touching your forehead, wash with water after 20 minutes.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-068GZE BLACK HAIR DYESHAMPOO (RESORCINOL) CREAM [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20240618_1b117713-db3a-7f2a-e063-6394a90a5bc8.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-06883566-068-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ASCORBIC ACIDPQ6CK8PD0RIACT
RESORCINOLYUL4LO94HKACTIB
STEARAMIDOETHYL ETHANOLAMINE MONOPHOSPHATEA3JOC2G06KACTIB
ACRYLATES CROSSPOLYMER-64GXD0Q3OS3IACT
CETEARETH-258FA93U5T67IACT
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
WATER059QF0KO0RIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
MANCHURIAN WALNUT SHELL98BYA5WZQQACTIB
ETIDRONIC ACIDM2F465ROXUIACT

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
39f49d38-35fc-b55c-e063-6294a90a54001b117713-db3a-7f2a-e063-6394a90a5bc82025-07-15WarningsExact identifier
spl set id: 1b117713-db3a-7f2a-e063-6394a90a5bc8

Reported adverse events (FAERS/openFDA)#

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