ALPET E3 PLUS 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: ALPET E3 PLUS HAND SANITIZER
Generic name: ALCOHOL
Manufacturer: Best Sanitizers, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d6d64945-4cd4-4926-9ef9-898cea89e811
SPL ID: 288c7d8c-bea8-22b0-e063-6394a90aa6b5
Version: 2
Effective date: 2024-12-05
Source export date: 2026-10-30
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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:39:14

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		ALPET E3 PLUS HAND SANITIZER	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Best Sanitizers, Inc.	openfda.manufacturer_name
ndc	package	59900-123-05	openfda.package_ndc
ndc	package	59900-123-04	openfda.package_ndc
ndc	package	59900-123-02	openfda.package_ndc
ndc	package	59900-123-09	openfda.package_ndc
ndc	package	59900-123-03	openfda.package_ndc
ndc	product	59900-123	openfda.product_ndc
ndc11	package	59900012305	derived:openfda.package_ndc
ndc11	package	59900012304	derived:openfda.package_ndc
ndc11	package	59900012309	derived:openfda.package_ndc
ndc11	package	59900012303	derived:openfda.package_ndc
ndc11	package	59900012302	derived:openfda.package_ndc
rxcui		1041882	openfda.rxcui
spl id		288c7d8c-bea8-22b0-e063-6394a90aa6b5	id
spl set id		d6d64945-4cd4-4926-9ef9-898cea89e811	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.