Uline 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: Uline Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Uline
Product type: HUMAN OTC DRUG
SPL set ID: a7aa3bde-d36e-f9d4-e053-2a95a90a6e6a
SPL ID: 5862330f-ec5f-1937-e063-6294a90a6c68
Version: 5
Effective date: 2026-08-06
Source export date: 2026-11-06
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/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 08:03:17

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Uline Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Uline	openfda.manufacturer_name
ndc	package	69790-801-04	openfda.package_ndc
ndc	product	69790-801	openfda.product_ndc
ndc11	package	69790080104	derived:openfda.package_ndc
rxcui		581662	openfda.rxcui
spl id		5862330f-ec5f-1937-e063-6294a90a6c68	id
spl set id		a7aa3bde-d36e-f9d4-e053-2a95a90a6e6a	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 Warnings • For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician. • 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.