Sani Luxe Hand Sanitizer with Alcohol

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 Hand Sanitizer with Alcohol
Generic name: ALCOHOL
Manufacturer: Celeste Industries Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 1a259dcf-4d82-4a42-be1f-0e557e0940bd
SPL ID: 1cc045e7-0007-22bc-e063-6394a90a11fa
Version: 13
Effective date: 2024-07-08
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 05:17:55

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 Hand Sanitizer with Alcohol	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Celeste Industries Corporation	openfda.manufacturer_name
ndc	package	71489-007-13	openfda.package_ndc
ndc	package	71489-007-01	openfda.package_ndc
ndc	package	71489-007-06	openfda.package_ndc
ndc	package	71489-007-16	openfda.package_ndc
ndc	package	71489-007-14	openfda.package_ndc
ndc	package	71489-007-08	openfda.package_ndc
ndc	package	71489-007-03	openfda.package_ndc
ndc	package	71489-007-15	openfda.package_ndc
ndc	package	71489-007-10	openfda.package_ndc
ndc	package	71489-007-11	openfda.package_ndc
ndc	package	71489-007-02	openfda.package_ndc
ndc	package	71489-007-05	openfda.package_ndc
ndc	package	71489-007-12	openfda.package_ndc
ndc	package	71489-007-07	openfda.package_ndc
ndc	package	71489-007-09	openfda.package_ndc
ndc	package	71489-007-04	openfda.package_ndc
ndc	product	71489-007	openfda.product_ndc
ndc11	package	71489000701	derived:openfda.package_ndc
ndc11	package	71489000710	derived:openfda.package_ndc
ndc11	package	71489000716	derived:openfda.package_ndc
ndc11	package	71489000715	derived:openfda.package_ndc
ndc11	package	71489000714	derived:openfda.package_ndc
ndc11	package	71489000702	derived:openfda.package_ndc
ndc11	package	71489000707	derived:openfda.package_ndc
ndc11	package	71489000708	derived:openfda.package_ndc
ndc11	package	71489000711	derived:openfda.package_ndc
ndc11	package	71489000704	derived:openfda.package_ndc
ndc11	package	71489000703	derived:openfda.package_ndc
ndc11	package	71489000713	derived:openfda.package_ndc
ndc11	package	71489000709	derived:openfda.package_ndc
ndc11	package	71489000712	derived:openfda.package_ndc
ndc11	package	71489000706	derived:openfda.package_ndc
ndc11	package	71489000705	derived:openfda.package_ndc
rxcui		1860080	openfda.rxcui
spl id		1cc045e7-0007-22bc-e063-6394a90a11fa	id
spl set id		1a259dcf-4d82-4a42-be1f-0e557e0940bd	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. Flammable. Keep away from open flame and sources of heat. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water. If swallowed, get medical help or contact a Poison Control Center right away. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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