ANTIBACTERIAL BANDAGES

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: ANTIBACTERIAL BANDAGES
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Guangdong Comfort Medical Products Co., Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: da241df2-6153-05e4-e053-2a95a90a0984
SPL ID: 310bdb8a-916f-6b80-e063-6394a90a4634
Version: 4
Effective date: 2025-03-26
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:42

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		ANTIBACTERIAL BANDAGES	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Guangdong Comfort Medical Products Co., Ltd.	openfda.manufacturer_name
ndc	package	71584-0111-4	openfda.package_ndc
ndc	package	71584-0111-7	openfda.package_ndc
ndc	package	71584-0111-6	openfda.package_ndc
ndc	package	71584-0111-2	openfda.package_ndc
ndc	package	71584-0111-3	openfda.package_ndc
ndc	package	71584-0111-8	openfda.package_ndc
ndc	package	71584-0111-1	openfda.package_ndc
ndc	package	71584-0111-5	openfda.package_ndc
ndc	product	71584-0111	openfda.product_ndc
ndc11	package	71584011105	derived:openfda.package_ndc
ndc11	package	71584011106	derived:openfda.package_ndc
ndc11	package	71584011107	derived:openfda.package_ndc
ndc11	package	71584011103	derived:openfda.package_ndc
ndc11	package	71584011108	derived:openfda.package_ndc
ndc11	package	71584011104	derived:openfda.package_ndc
ndc11	package	71584011101	derived:openfda.package_ndc
ndc11	package	71584011102	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		310bdb8a-916f-6b80-e063-6394a90a4634	id
spl set id		da241df2-6153-05e4-e053-2a95a90a0984	set_id
unii		F5UM2KM3W7	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS For external use only. Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a physician. In case of deep or puncture wounds, animal bites, or serious burn, consult a physician. Keep out of reach of children. if swallowed get medical help or contact Poison control Center right away.

Reported adverse events (FAERS/openFDA)#

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