ALPET QE2 SANITIZING 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: ALPET QE2 SANITIZING FOAM
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Best Sanitizers, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 0aa71f9d-f660-4a32-b54a-1968aea9d0ee
SPL ID: 288e37ae-012f-23f8-e063-6394a90a586b
Version: 2
Effective date: 2024-12-05
Source export date: 2026-10-30
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:49:06

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		ALPET QE2 SANITIZING FOAM	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Best Sanitizers, Inc.	openfda.manufacturer_name
ndc	package	59900-214-10	openfda.package_ndc
ndc	package	59900-214-03	openfda.package_ndc
ndc	package	59900-214-01	openfda.package_ndc
ndc	package	59900-214-02	openfda.package_ndc
ndc	package	59900-214-05	openfda.package_ndc
ndc	package	59900-214-08	openfda.package_ndc
ndc	product	59900-214	openfda.product_ndc
ndc11	package	59900021408	derived:openfda.package_ndc
ndc11	package	59900021410	derived:openfda.package_ndc
ndc11	package	59900021405	derived:openfda.package_ndc
ndc11	package	59900021403	derived:openfda.package_ndc
ndc11	package	59900021402	derived:openfda.package_ndc
ndc11	package	59900021401	derived:openfda.package_ndc
rxcui		1053188	openfda.rxcui
spl id		288e37ae-012f-23f8-e063-6394a90a586b	id
spl set id		0aa71f9d-f660-4a32-b54a-1968aea9d0ee	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 do not use in or near eyes Stop use and ask a doctor if irritation or redness develop. Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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