Purifi 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: Purifi Hand Sanitizer
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Purifi LLC
Product type: HUMAN OTC DRUG
SPL set ID: 9267069d-4cf5-4e48-a446-7dbebea16bf5
SPL ID: 103dc041-e75d-b464-e063-6394a90ab4d8
Version: 4
Effective date: 2024-01-31
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:56:29

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Purifi Hand Sanitizer	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Purifi LLC	openfda.manufacturer_name
ndc	package	80659-301-03	openfda.package_ndc
ndc	package	80659-301-04	openfda.package_ndc
ndc	package	80659-301-02	openfda.package_ndc
ndc	package	80659-301-01	openfda.package_ndc
ndc	package	80659-301-05	openfda.package_ndc
ndc	product	80659-301	openfda.product_ndc
ndc11	package	80659030101	derived:openfda.package_ndc
ndc11	package	80659030103	derived:openfda.package_ndc
ndc11	package	80659030104	derived:openfda.package_ndc
ndc11	package	80659030105	derived:openfda.package_ndc
ndc11	package	80659030102	derived:openfda.package_ndc
rxcui		1049254	openfda.rxcui
spl id		103dc041-e75d-b464-e063-6394a90ab4d8	id
spl set id		9267069d-4cf5-4e48-a446-7dbebea16bf5	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 the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or redness appears and lasts 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.