E2 SANITIZING HAND

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: E2 SANITIZING HAND
Generic name: E2 SANITIZING HAND
Manufacturer: KUTOL PRODUCTS COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 70357eaf-8cd8-4c5e-b7a8-ae2fbba0ca2e
SPL ID: 298f1da8-676b-6cb9-e063-6294a90a78ab
Version: 9
Effective date: 2024-12-18
Source export date: 2026-10-30
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/2026-10-30/a900515c00f4d0d29f88cc94ee68daf127f036296f87a6b4a8a3f964cd0433c0/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:49:06

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		E2 SANITIZING HAND	openfda.brand_name
generic name		E2 SANITIZING HAND	openfda.generic_name
manufacturer name		KUTOL PRODUCTS COMPANY	openfda.manufacturer_name
ndc	package	50865-017-65	openfda.package_ndc
ndc	package	50865-017-03	openfda.package_ndc
ndc	package	50865-017-09	openfda.package_ndc
ndc	package	50865-017-41	openfda.package_ndc
ndc	package	50865-017-07	openfda.package_ndc
ndc	package	50865-017-67	openfda.package_ndc
ndc	product	50865-017	openfda.product_ndc
ndc11	package	50865001741	derived:openfda.package_ndc
ndc11	package	50865001765	derived:openfda.package_ndc
ndc11	package	50865001709	derived:openfda.package_ndc
ndc11	package	50865001767	derived:openfda.package_ndc
ndc11	package	50865001703	derived:openfda.package_ndc
ndc11	package	50865001707	derived:openfda.package_ndc
spl id		298f1da8-676b-6cb9-e063-6294a90a78ab	id
spl set id		70357eaf-8cd8-4c5e-b7a8-ae2fbba0ca2e	set_id
unii		F5UM2KM3W7	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. Avoid contact with eyes. If contact occurs, flush with water. Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours. 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.