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: Broder Bros Co.
Product type: HUMAN OTC DRUG
SPL set ID: b8183dae-4cdc-c369-e053-2995a90a75c4
SPL ID: 43d13e36-df5e-eee2-e063-6394a90a60cf
Version: 5
Effective date: 2025-11-17
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 06:38:47

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Antibacterial Hand Sanitizer	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		Broder Bros Co.	openfda.manufacturer_name
ndc	package	71513-105-03	openfda.package_ndc
ndc	package	71513-105-01	openfda.package_ndc
ndc	package	71513-105-05	openfda.package_ndc
ndc	package	71513-105-50	openfda.package_ndc
ndc	package	71513-105-04	openfda.package_ndc
ndc	package	71513-105-06	openfda.package_ndc
ndc	product	71513-105	openfda.product_ndc
ndc11	package	71513010506	derived:openfda.package_ndc
ndc11	package	71513010550	derived:openfda.package_ndc
ndc11	package	71513010504	derived:openfda.package_ndc
ndc11	package	71513010505	derived:openfda.package_ndc
ndc11	package	71513010501	derived:openfda.package_ndc
ndc11	package	71513010503	derived:openfda.package_ndc
rxcui		581660	openfda.rxcui
spl id		43d13e36-df5e-eee2-e063-6394a90a60cf	id
spl set id		b8183dae-4cdc-c369-e053-2995a90a75c4	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 heat and flame. For external use only When using this product Keep out of eyes In case of contact with eyes, flush thoroughly with water Avoid contact with broken skin Do not inhale or ingest Stop use and ask a doctor if irritation and redness develops and persists for more than 72 hours Keep out of reach of children if swallowed, get medical help promptly and contact Poison Control

Reported adverse events (FAERS/openFDA)#

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