Sanell 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: Sanell Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: OraLabs
Product type: HUMAN OTC DRUG
SPL set ID: 0a6cc2a8-f568-45ae-8d82-a70103c774c7
SPL ID: 33dd4273-5402-5be0-e063-6394a90a41c1
Version: 3
Effective date: 2025-04-28
Source export date: 2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:53:43

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Sanell Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		OraLabs	openfda.manufacturer_name
ndc	package	63645-174-02	openfda.package_ndc
ndc	product	63645-174	openfda.product_ndc
ndc11	package	63645017402	derived:openfda.package_ndc
rxcui		1798385	openfda.rxcui
spl id		33dd4273-5402-5be0-e063-6394a90a41c1	id
spl set id		0a6cc2a8-f568-45ae-8d82-a70103c774c7	set_id
unii		3K9958V90M	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: Hands. Flammable. Keep away from fire or flame. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor: if irritation and redness develop and persists for more than 72 hours.

Reported adverse events (FAERS/openFDA)#

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