eZFoam Foaming Alcohol 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: eZFoam Foaming Alcohol Hand Sanitizer
Generic name: FOAMING HAND SANITIZER
Manufacturer: Kutol Products Company
Product type: HUMAN OTC DRUG
SPL set ID: 1f56b4c5-d703-4193-83a8-3be815c8acda
SPL ID: 298e167d-7005-98da-e063-6294a90a07ba
Version: 6
Effective date: 2024-12-18
Source export date: 2026-10-27
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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:01:38

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		eZFoam Foaming Alcohol Hand Sanitizer	openfda.brand_name
generic name		FOAMING HAND SANITIZER	openfda.generic_name
manufacturer name		Kutol Products Company	openfda.manufacturer_name
ndc	package	50865-688-03	openfda.package_ndc
ndc	package	50865-688-17	openfda.package_ndc
ndc	package	50865-688-91	openfda.package_ndc
ndc	package	50865-688-09	openfda.package_ndc
ndc	package	50865-688-78	openfda.package_ndc
ndc	package	50865-688-24	openfda.package_ndc
ndc	package	50865-688-50	openfda.package_ndc
ndc	package	50865-688-41	openfda.package_ndc
ndc	product	50865-688	openfda.product_ndc
ndc11	package	50865068850	derived:openfda.package_ndc
ndc11	package	50865068809	derived:openfda.package_ndc
ndc11	package	50865068891	derived:openfda.package_ndc
ndc11	package	50865068841	derived:openfda.package_ndc
ndc11	package	50865068817	derived:openfda.package_ndc
ndc11	package	50865068824	derived:openfda.package_ndc
ndc11	package	50865068803	derived:openfda.package_ndc
ndc11	package	50865068878	derived:openfda.package_ndc
rxcui		616763	openfda.rxcui
spl id		298e167d-7005-98da-e063-6294a90a07ba	id
spl set id		1f56b4c5-d703-4193-83a8-3be815c8acda	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

For external use only. FLAMMABLE. Keep away from heat or flames. Avoid contact with eyes. If eye contact occurs, flush with water. Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, contact a physician or poison control center.

Reported adverse events (FAERS/openFDA)#

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