Premium Hand Sanitizer with Aloe

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: Premium Hand Sanitizer with Aloe
Generic name: ETHANOL
Manufacturer: MCKESSON MEDICAL-SURGICAL INC.
Product type: HUMAN OTC DRUG
SPL set ID: 13d42582-df02-41d5-bada-1d67c6131015
SPL ID: 3ca30e4b-f024-f83c-e063-6394a90a2f95
Version: 9
Effective date: 2025-08-18
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:44:48

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Premium Hand Sanitizer with Aloe	openfda.brand_name
generic name		ETHANOL	openfda.generic_name
manufacturer name		MCKESSON MEDICAL-SURGICAL INC.	openfda.manufacturer_name
ndc	package	68599-5202-6	openfda.package_ndc
ndc	package	68599-5202-5	openfda.package_ndc
ndc	package	68599-5202-2	openfda.package_ndc
ndc	package	68599-5202-3	openfda.package_ndc
ndc	package	68599-5202-1	openfda.package_ndc
ndc	package	68599-5202-4	openfda.package_ndc
ndc	package	68599-5202-7	openfda.package_ndc
ndc	product	68599-5202	openfda.product_ndc
ndc11	package	68599520206	derived:openfda.package_ndc
ndc11	package	68599520202	derived:openfda.package_ndc
ndc11	package	68599520201	derived:openfda.package_ndc
ndc11	package	68599520207	derived:openfda.package_ndc
ndc11	package	68599520205	derived:openfda.package_ndc
ndc11	package	68599520204	derived:openfda.package_ndc
ndc11	package	68599520203	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		3ca30e4b-f024-f83c-e063-6394a90a2f95	id
spl set id		13d42582-df02-41d5-bada-1d67c6131015	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. Flammable, keep away from fire or flame. When using this product avoid contact with eyes. In case of eye contact, flush with water for 15 minutes. Discontinue use and see a doctor if irritation occurs. Avoid contact with broken skin.

Reported adverse events (FAERS/openFDA)#

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