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: Zhejiang Ayan Biotech Co.,Ltd.
Product type: HUMAN OTC DRUG
SPL set ID: 27dd30e7-3e2c-4409-9cf1-66db27611c1b
SPL ID: 0986c648-5f24-7c4c-e063-6394a90abd3d
Version: 5
Effective date: 2023-11-06
Source export date: 2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:32:20

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 · 27 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		Zhejiang Ayan Biotech Co.,Ltd.	openfda.manufacturer_name
ndc	package	70412-119-25	openfda.package_ndc
ndc	package	70412-119-30	openfda.package_ndc
ndc	package	70412-119-05	openfda.package_ndc
ndc	package	70412-119-12	openfda.package_ndc
ndc	package	70412-119-20	openfda.package_ndc
ndc	package	70412-119-08	openfda.package_ndc
ndc	package	70412-119-03	openfda.package_ndc
ndc	package	70412-119-16	openfda.package_ndc
ndc	package	70412-119-10	openfda.package_ndc
ndc	product	70412-119	openfda.product_ndc
ndc11	package	70412011908	derived:openfda.package_ndc
ndc11	package	70412011903	derived:openfda.package_ndc
ndc11	package	70412011905	derived:openfda.package_ndc
ndc11	package	70412011930	derived:openfda.package_ndc
ndc11	package	70412011925	derived:openfda.package_ndc
ndc11	package	70412011912	derived:openfda.package_ndc
ndc11	package	70412011920	derived:openfda.package_ndc
ndc11	package	70412011910	derived:openfda.package_ndc
ndc11	package	70412011916	derived:openfda.package_ndc
rxcui		1020364	openfda.rxcui
spl id		0986c648-5f24-7c4c-e063-6394a90abd3d	id
spl set id		27dd30e7-3e2c-4409-9cf1-66db27611c1b	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. Do not apply around eyes, Do not use in ears & mouth. When using this product, avoid contact with eyes. In case of contact flush eyes with water. Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. Keep out of reach of children. Children must be supervised in use of this product.

Reported adverse events (FAERS/openFDA)#

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