Antibacterial Bar - Guangzhou Zeshi Daily Chemical Co.,Ltd.

Manufacturer
Guangzhou Zeshi Daily Chemical Co.,Ltd.
Effective date
2026-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-03 03:01:06

Label at a glance#

ProductAntibacterial Bar
Active ingredientBENZETHONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride

WARNINGS SECTION

keep out of reach of chilsren

OTC - PURPOSE SECTION

Antibacterial

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

INACTIVE INGREDIENT SECTION

Sodium Palmate,Sodium Palm Kernelate,Sodium Cocoate,Calcium Carbonate,Water,Glycerin,Sodium Chloride,Tetrasodium EDTA,Etidronate Tetrasodium,Fragrance

DOSAGE & ADMINISTRATION SECTION

Wet skin with water. Apply bar soap and lather. Rinse thoroughly.

For external use only. Avoid contact with eyes.

INDICATIONS & USAGE SECTION

Wet skin with water. Apply bar soap and lather. Rinse thoroughly.

For external use only. Avoid contact with eyes.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3344

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
87981-20387981-203-11

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
Antibacterial BarANTIBACTERIAL BARGuangzhou Zeshi Daily Chemical Co.,Ltd.5a6f7c00-1dde-26b6-e063-6294a90a19e72026-09-01WarningsExact identifier
ndc (package): 87981-203-11
ndc (product): 87981-203
ndc11 (package): 87981020311
spl id: 5a6f7c00-1ddf-26b6-e063-6294a90a19e7
spl set id: 5a6f7c00-1dde-26b6-e063-6294a90a19e7

Reported adverse events (FAERS/openFDA)#

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