Foaming 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: Foaming Sanitizing Hand
Generic name: ALCOHOL
Manufacturer: Kutol Products Company
Product type: HUMAN OTC DRUG
SPL set ID: b2e22e51-88f5-4391-8705-3855c1645d80
SPL ID: 50375794-9187-674e-e063-6394a90a6dff
Version: 9
Effective date: 2026-04-24
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:13:38

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Foaming Sanitizing Hand	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Kutol Products Company	openfda.manufacturer_name
ndc	package	50865-710-41	openfda.package_ndc
ndc	package	50865-710-55	openfda.package_ndc
ndc	package	50865-710-92	openfda.package_ndc
ndc	package	50865-710-17	openfda.package_ndc
ndc	package	50865-710-91	openfda.package_ndc
ndc	package	50865-710-44	openfda.package_ndc
ndc	product	50865-710	openfda.product_ndc
ndc11	package	50865071044	derived:openfda.package_ndc
ndc11	package	50865071017	derived:openfda.package_ndc
ndc11	package	50865071091	derived:openfda.package_ndc
ndc11	package	50865071055	derived:openfda.package_ndc
ndc11	package	50865071092	derived:openfda.package_ndc
ndc11	package	50865071041	derived:openfda.package_ndc
spl id		50375794-9187-674e-e063-6394a90a6dff	id
spl set id		b2e22e51-88f5-4391-8705-3855c1645d80	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 heat or flames. Avoid contact with eyes. If eye contact occurs, flush eyes with water. Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

Reported adverse events (FAERS/openFDA)#

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