Altra Foaming Hand Sanitizer with Aloe and Vitamin E

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: Altra Foaming Hand Sanitizer with Aloe and Vitamin E
Generic name: ALCOHOL
Manufacturer: Buckeye International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a28ff21e-a507-8257-e053-2a95a90afd4e
SPL ID: 31315ef1-88b5-53b8-e063-6394a90acb1d
Version: 3
Effective date: 2025-03-25
Source export date: 2026-10-12
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:26:31

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		505G(a)(3)	openfda.application_number
brand name		Altra Foaming Hand Sanitizer with Aloe and Vitamin E	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Buckeye International, Inc.	openfda.manufacturer_name
ndc	package	30805-012-09	openfda.package_ndc
ndc	package	30805-012-04	openfda.package_ndc
ndc	package	30805-012-13	openfda.package_ndc
ndc	package	30805-012-07	openfda.package_ndc
ndc	package	30805-012-05	openfda.package_ndc
ndc	product	30805-012	openfda.product_ndc
ndc11	package	30805001213	derived:openfda.package_ndc
ndc11	package	30805001209	derived:openfda.package_ndc
ndc11	package	30805001205	derived:openfda.package_ndc
ndc11	package	30805001204	derived:openfda.package_ndc
ndc11	package	30805001207	derived:openfda.package_ndc
rxcui		616763	openfda.rxcui
spl id		31315ef1-88b5-53b8-e063-6394a90acb1d	id
spl set id		a28ff21e-a507-8257-e053-2a95a90afd4e	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 Flammable, Keep away from fire or flame. For external use only. When using this product do not use in or near eyes. If in eyes, flush thoroughly with water. If irritation or rash appears and persists , stop use and see a physician. Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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