FoamFresh E-2 Sanitizer Cleanser

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: FoamFresh E-2 Sanitizer Cleanser
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Woodbine Products Company
Product type: HUMAN OTC DRUG
SPL set ID: c49f49ad-06fc-4759-9ac9-1f1e29d8c2cf
SPL ID: 27c452b3-328a-15ac-e063-6394a90ab589
Version: 5
Effective date: 2024-11-25
Source export date: 2026-10-12
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:25:18

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		FoamFresh E-2 Sanitizer Cleanser	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Woodbine Products Company	openfda.manufacturer_name
ndc	package	11429-1002-7	openfda.package_ndc
ndc	package	11429-1002-3	openfda.package_ndc
ndc	package	11429-1002-8	openfda.package_ndc
ndc	package	11429-1002-6	openfda.package_ndc
ndc	package	11429-1002-0	openfda.package_ndc
ndc	package	11429-1002-9	openfda.package_ndc
ndc	product	11429-1002	openfda.product_ndc
ndc11	package	11429100209	derived:openfda.package_ndc
ndc11	package	11429100207	derived:openfda.package_ndc
ndc11	package	11429100200	derived:openfda.package_ndc
ndc11	package	11429100208	derived:openfda.package_ndc
ndc11	package	11429100203	derived:openfda.package_ndc
ndc11	package	11429100206	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		27c452b3-328a-15ac-e063-6394a90ab589	id
spl set id		c49f49ad-06fc-4759-9ac9-1f1e29d8c2cf	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 or redness develops, or if condition persists for more than 72 hours. 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.