Germfree24 Hand Sanitizer

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: Germfree24 Hand Sanitizer
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: fb43545b-6ddc-49fb-86dd-17cd1a925a78
SPL ID: 85ae296d-418e-4fc0-9dfd-198111245281
Version: 3
Effective date: 2026-07-22
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:25

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Germfree24 Hand Sanitizer	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-016-04	openfda.package_ndc
ndc	package	71884-016-06	openfda.package_ndc
ndc	package	71884-016-03	openfda.package_ndc
ndc	package	71884-016-05	openfda.package_ndc
ndc	package	71884-016-02	openfda.package_ndc
ndc	package	71884-016-01	openfda.package_ndc
ndc	product	71884-016	openfda.product_ndc
ndc11	package	71884001604	derived:openfda.package_ndc
ndc11	package	71884001606	derived:openfda.package_ndc
ndc11	package	71884001605	derived:openfda.package_ndc
ndc11	package	71884001602	derived:openfda.package_ndc
ndc11	package	71884001601	derived:openfda.package_ndc
ndc11	package	71884001603	derived:openfda.package_ndc
rxcui		1039012	openfda.rxcui
spl id		85ae296d-418e-4fc0-9dfd-198111245281	id
spl set id		fb43545b-6ddc-49fb-86dd-17cd1a925a78	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: Do not freeze. For external use only. Do not use in ears, eyes or mouth. • When using this product, avoid contact with eyes. In case of contact, flush eyes with water. • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. • Keep out of reach of children. • Children should be supervised when using this product.

Reported adverse events (FAERS/openFDA)#

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