Extra Stength Hand Sanitizer Zytec Germ Buster

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: Extra Stength Hand Sanitizer Zytec Germ Buster
Generic name: ALCOHOL 80%W/W
Manufacturer: Empack Spraytech Inc.
Product type: HUMAN OTC DRUG
SPL set ID: da854195-3a50-4fae-a5ea-183bf524c973
SPL ID: 20af5ae7-2a91-ff8d-e063-6394a90ad503
Version: 6
Effective date: 2024-12-12
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:44

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		M003	openfda.application_number
brand name		Extra Stength Hand Sanitizer Zytec Germ Buster	openfda.brand_name
generic name		ALCOHOL 80%W/W	openfda.generic_name
manufacturer name		Empack Spraytech Inc.	openfda.manufacturer_name
ndc	package	50021-008-07	openfda.package_ndc
ndc	package	50021-008-03	openfda.package_ndc
ndc	package	50021-008-06	openfda.package_ndc
ndc	package	50021-008-04	openfda.package_ndc
ndc	package	50021-008-01	openfda.package_ndc
ndc	package	50021-008-09	openfda.package_ndc
ndc	package	50021-008-02	openfda.package_ndc
ndc	package	50021-008-05	openfda.package_ndc
ndc	package	50021-008-08	openfda.package_ndc
ndc	product	50021-008	openfda.product_ndc
ndc11	package	50021000801	derived:openfda.package_ndc
ndc11	package	50021000806	derived:openfda.package_ndc
ndc11	package	50021000808	derived:openfda.package_ndc
ndc11	package	50021000805	derived:openfda.package_ndc
ndc11	package	50021000809	derived:openfda.package_ndc
ndc11	package	50021000803	derived:openfda.package_ndc
ndc11	package	50021000804	derived:openfda.package_ndc
ndc11	package	50021000807	derived:openfda.package_ndc
ndc11	package	50021000802	derived:openfda.package_ndc
rxcui		1241663	openfda.rxcui
spl id		20af5ae7-2a91-ff8d-e063-6394a90ad503	id
spl set id		da854195-3a50-4fae-a5ea-183bf524c973	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 use in children less than 2 months age on open skin wounds Stop use and ask a doctor if rash occurs. When using this product keep out of eyes, ears, and mouth. in case of contact with eyes, rinse with water Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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