FDA.reportPublic FDA data

GZE HAIR POMADE

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd. | Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:30

Label at a glance#

ProductGZE HAIR POMADE
Active ingredientBIOTIN
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Biotin 2.71%

INACTIVE INGREDIENT SECTION

Aqua

Petrolatum

Cetyl Alcohol

Hydroxyethylcellulose

Serenoa Serrulata Fruit Extract

OTC - PURPOSE SECTION

Hair styling.

INDICATIONS & USAGE SECTION

Emulsify pomade in hands, apply pomade to hair, style as desired.

WARNINGS SECTION

1. 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

1. 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

Emulsify pomade in hands, apply pomade to hair, style as desired.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-249GZE HAIR POMADE (BIOTIN) PASTE [GUANGZHOU YILONG COSMETICS CO.,LTD.]1Unmatched20240820_20065d97-a202-2af8-e063-6294a90ab8dd.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-24983566-249-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
BIOTIN6SO6U10H04ACTIB
PETROLATUM4T6H12BN9UIACT
WATER059QF0KO0RIACT
SAW PALMETTOJ7WWH9M8QSIACT
CETYL ALCOHOL936JST6JCNIACT

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
39f64c5d-d89d-beed-e063-6394a90aecc620065d97-a202-2af8-e063-6294a90ab8dd2025-07-15WarningsExact identifier
spl set id: 20065d97-a202-2af8-e063-6294a90ab8dd

Reported adverse events (FAERS/openFDA)#

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