Antibacterial Foam

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 Foam
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: SC Johnson Professional USA Inc.
Product type: HUMAN OTC DRUG
SPL set ID: df36ccda-b9cb-41ba-8d4d-56ec447e63df
SPL ID: 70390f59-9b71-4614-be06-57ae24e8ec5c
Version: 11
Effective date: 2025-12-23
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:36:03

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Antibacterial Foam	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		SC Johnson Professional USA Inc.	openfda.manufacturer_name
ndc	package	11084-021-55	openfda.package_ndc
ndc	package	11084-021-42	openfda.package_ndc
ndc	package	11084-021-05	openfda.package_ndc
ndc	product	11084-021	openfda.product_ndc
ndc11	package	11084002155	derived:openfda.package_ndc
ndc11	package	11084002105	derived:openfda.package_ndc
ndc11	package	11084002142	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		70390f59-9b71-4614-be06-57ae24e8ec5c	id
spl set id		df36ccda-b9cb-41ba-8d4d-56ec447e63df	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 When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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