ALPET E3 HAND SANITIZER FOAM

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: ALPET E3 HAND SANITIZER FOAM
Generic name: ALCOHOL
Manufacturer: Best Sanitizers, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 53573e1a-a3f8-4598-8248-ec4a62392d00
SPL ID: 288cba7a-1f65-6d80-e063-6394a90aca47
Version: 3
Effective date: 2024-12-05
Source export date: 2026-10-30
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/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:45:20

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		ALPET E3 HAND SANITIZER FOAM	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Best Sanitizers, Inc.	openfda.manufacturer_name
ndc	package	59900-125-05	openfda.package_ndc
ndc	package	59900-125-02	openfda.package_ndc
ndc	package	59900-125-08	openfda.package_ndc
ndc	package	59900-125-03	openfda.package_ndc
ndc	product	59900-125	openfda.product_ndc
ndc11	package	59900012508	derived:openfda.package_ndc
ndc11	package	59900012502	derived:openfda.package_ndc
ndc11	package	59900012505	derived:openfda.package_ndc
ndc11	package	59900012503	derived:openfda.package_ndc
rxcui		616763	openfda.rxcui
spl id		288cba7a-1f65-6d80-e063-6394a90aca47	id
spl set id		53573e1a-a3f8-4598-8248-ec4a62392d00	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 do not use in or near eyes use in a well-ventilated area Stop use and consult a doctor if irritation or redness develop. Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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