Refresh AntiBac 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: Refresh AntiBac FOAM
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: SC Johnson Professional USA Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 884d1c8c-5643-423e-8ed4-d2ef38f8af73
SPL ID: 1efa3243-2522-4796-9891-a61fc315ea00
Version: 12
Effective date: 2026-08-13
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:15:25

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Refresh AntiBac FOAM	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		SC Johnson Professional USA Inc.	openfda.manufacturer_name
ndc	package	11084-010-05	openfda.package_ndc
ndc	package	11084-010-01	openfda.package_ndc
ndc	package	11084-010-40	openfda.package_ndc
ndc	package	11084-010-66	openfda.package_ndc
ndc	package	11084-010-96	openfda.package_ndc
ndc	package	11084-010-12	openfda.package_ndc
ndc	package	11084-010-55	openfda.package_ndc
ndc	package	11084-010-20	openfda.package_ndc
ndc	package	11084-010-27	openfda.package_ndc
ndc	product	11084-010	openfda.product_ndc
ndc11	package	11084001040	derived:openfda.package_ndc
ndc11	package	11084001005	derived:openfda.package_ndc
ndc11	package	11084001066	derived:openfda.package_ndc
ndc11	package	11084001055	derived:openfda.package_ndc
ndc11	package	11084001001	derived:openfda.package_ndc
ndc11	package	11084001027	derived:openfda.package_ndc
ndc11	package	11084001096	derived:openfda.package_ndc
ndc11	package	11084001020	derived:openfda.package_ndc
ndc11	package	11084001012	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		1efa3243-2522-4796-9891-a61fc315ea00	id
spl set id		884d1c8c-5643-423e-8ed4-d2ef38f8af73	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.