Sani Luxe Foaming Hand Sanitizer Alcohol Free

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: Sani Luxe Foaming Hand Sanitizer Alcohol Free
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Celeste Industries Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 7549428e-b10f-45b9-b414-0c6e8b41c398
SPL ID: 1cbe491e-af31-8dd8-e063-6394a90ae2f5
Version: 10
Effective date: 2024-07-08
Source export date: 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:31:05

Harmonized routes table
Harmonized routes
CUTANEOUS

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 2 · 41 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Sani Luxe Foaming Hand Sanitizer Alcohol Free	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Celeste Industries Corporation	openfda.manufacturer_name
ndc	package	71489-006-11	openfda.package_ndc
ndc	package	71489-006-08	openfda.package_ndc
ndc	package	71489-006-02	openfda.package_ndc
ndc	package	71489-006-06	openfda.package_ndc
ndc	package	71489-006-09	openfda.package_ndc
ndc	package	71489-006-16	openfda.package_ndc
ndc	package	71489-006-10	openfda.package_ndc
ndc	package	71489-006-04	openfda.package_ndc
ndc	package	71489-006-05	openfda.package_ndc
ndc	package	71489-006-01	openfda.package_ndc
ndc	package	71489-006-12	openfda.package_ndc
ndc	package	71489-006-03	openfda.package_ndc
ndc	package	71489-006-13	openfda.package_ndc
ndc	package	71489-006-07	openfda.package_ndc
ndc	package	71489-006-14	openfda.package_ndc
ndc	package	71489-006-15	openfda.package_ndc
ndc	product	71489-006	openfda.product_ndc
ndc11	package	71489000606	derived:openfda.package_ndc
ndc11	package	71489000601	derived:openfda.package_ndc
ndc11	package	71489000612	derived:openfda.package_ndc
ndc11	package	71489000605	derived:openfda.package_ndc
ndc11	package	71489000611	derived:openfda.package_ndc
ndc11	package	71489000602	derived:openfda.package_ndc
ndc11	package	71489000616	derived:openfda.package_ndc
ndc11	package	71489000603	derived:openfda.package_ndc
ndc11	package	71489000609	derived:openfda.package_ndc
ndc11	package	71489000607	derived:openfda.package_ndc
ndc11	package	71489000608	derived:openfda.package_ndc
ndc11	package	71489000604	derived:openfda.package_ndc
ndc11	package	71489000610	derived:openfda.package_ndc
ndc11	package	71489000615	derived:openfda.package_ndc
ndc11	package	71489000614	derived:openfda.package_ndc
ndc11	package	71489000613	derived:openfda.package_ndc
rxcui		1038799	openfda.rxcui
spl id		1cbe491e-af31-8dd8-e063-6394a90ae2f5	id
spl set id		7549428e-b10f-45b9-b414-0c6e8b41c398	set_id

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. Keep out of reach of children. When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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