Antimicrobial Foaming Hand

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: Antimicrobial Foaming Hand
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Health Technology Professional Products, Inc
Product type: HUMAN OTC DRUG
SPL set ID: dbca0970-88ca-04a4-e053-2995a90a68f2
SPL ID: 2fbac9d4-5f01-0ce7-e063-6394a90a3573
Version: 3
Effective date: 2025-03-07
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:21

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		Antimicrobial Foaming Hand	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Health Technology Professional Products, Inc	openfda.manufacturer_name
ndc	package	81775-100-03	openfda.package_ndc
ndc	package	81775-100-01	openfda.package_ndc
ndc	package	81775-100-02	openfda.package_ndc
ndc	product	81775-100	openfda.product_ndc
ndc11	package	81775010002	derived:openfda.package_ndc
ndc11	package	81775010003	derived:openfda.package_ndc
ndc11	package	81775010001	derived:openfda.package_ndc
rxcui		1046593	openfda.rxcui
spl id		2fbac9d4-5f01-0ce7-e063-6394a90a3573	id
spl set id		dbca0970-88ca-04a4-e053-2995a90a68f2	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 contact flush eyes with water. Do not ingest, Stop use and ask a doctor if irritation or redness develop and condition persists. Keep Out Of Reach Of Children If swallowed get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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