Germ Free 24 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: Germ Free 24 Hand Sanitizer
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Enviro Specialty Chemicals Inc
Product type: HUMAN OTC DRUG
SPL set ID: fa0cb8a1-d58a-4c7a-928e-2b071d9dd3ee
SPL ID: a0f2af94-0b98-4703-b048-382ca294dbdb
Version: 7
Effective date: 2026-07-21
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:28:19

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		Germ Free 24 Hand Sanitizer	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Enviro Specialty Chemicals Inc	openfda.manufacturer_name
ndc	package	71884-006-01	openfda.package_ndc
ndc	package	71884-006-07	openfda.package_ndc
ndc	package	71884-006-09	openfda.package_ndc
ndc	package	71884-006-08	openfda.package_ndc
ndc	package	71884-006-10	openfda.package_ndc
ndc	package	71884-006-11	openfda.package_ndc
ndc	product	71884-006	openfda.product_ndc
ndc11	package	71884000609	derived:openfda.package_ndc
ndc11	package	71884000611	derived:openfda.package_ndc
ndc11	package	71884000601	derived:openfda.package_ndc
ndc11	package	71884000607	derived:openfda.package_ndc
ndc11	package	71884000610	derived:openfda.package_ndc
ndc11	package	71884000608	derived:openfda.package_ndc
rxcui		1020365	openfda.rxcui
spl id		a0f2af94-0b98-4703-b048-382ca294dbdb	id
spl set id		fa0cb8a1-d58a-4c7a-928e-2b071d9dd3ee	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 the 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.