ANTIBACTERIAL 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: ANTIBACTERIAL HAND SANITIZER
Generic name: ETHYL ALCOHOL
Manufacturer: ASC Marketing Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: b42ebe64-0cad-2d26-e053-2a95a90af3dd
SPL ID: 3239bc65-ad79-c7d7-e063-6394a90a26a2
Version: 2
Effective date: 2025-04-07
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:15

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		ANTIBACTERIAL HAND SANITIZER	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		ASC Marketing Ltd.	openfda.manufacturer_name
ndc	package	73145-009-01	openfda.package_ndc
ndc	product	73145-009	openfda.product_ndc
ndc11	package	73145000901	derived:openfda.package_ndc
spl id		3239bc65-ad79-c7d7-e063-6394a90a26a2	id
spl set id		b42ebe64-0cad-2d26-e053-2a95a90af3dd	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 and flame. For external use only. Do not use in eyes. In case of contact，rinse eyes thoroughly with water. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours consult a doctor.

Reported adverse events (FAERS/openFDA)#

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