GZE BRAID FOAM CONTROL

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:56:29

Label at a glance#

ProductGZE BRAID FOAM CONTROL
Active ingredientHYDROGENATED CASTOR OIL, GRAPE SEED OIL, JOJOBA OIL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

PEG-40 Hydrogenated Castor Oil 5%

Vitis Vinifera (Grape) Seed Oil 3%

Simmondsia Chinensis (Jojoba) Seed Oil 2%

INACTIVE INGREDIENT SECTION

Water

Cocamidopropyl Betaine

Methyl Benzoate

Propylene Glycol

Fragrance

Diazolidinyl Urea

OTC - PURPOSE SECTION

Long-lasting hairstyles.

Moisturizes and maintains shine.

INDICATIONS & USAGE SECTION

Apply braid foam to your finished braided hairstyle.Gently incorporate the foam into your braids while gliding and patting it in carefully.

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 braid foam to your finished braided hairstyle.Gently incorporate the foam into your braids while gliding and patting it in carefully.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-075GZE BRAID FOAM CONTROL (PEG-40 HYDROGENATED CASTOR OIL) LIQUID [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20240820_2001a450-c608-2c27-e063-6394a90a9ab4.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-07583566-075-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
39f60b5e-08f6-bedb-e063-6394a90a53ec2001a450-c608-2c27-e063-6394a90a9ab42025-07-15WarningsExact identifier
spl set id: 2001a450-c608-2c27-e063-6394a90a9ab4

Reported adverse events (FAERS/openFDA)#

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