Kleenex Ultra Moisturizing 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: Kleenex Ultra Moisturizing Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Kimberly-Clark Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 75e884bf-8e0d-41e7-adbb-4400ee3d1e07
SPL ID: 92ebe19a-e5cd-40cb-89ec-60d675a726d3
Version: 8
Effective date: 2026-05-08
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 05:55:31

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		Kleenex Ultra Moisturizing Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Kimberly-Clark Corporation	openfda.manufacturer_name
ndc	package	55118-530-91	openfda.package_ndc
ndc	package	55118-530-10	openfda.package_ndc
ndc	package	55118-530-65	openfda.package_ndc
ndc	package	55118-530-88	openfda.package_ndc
ndc	package	55118-530-11	openfda.package_ndc
ndc	package	55118-530-99	openfda.package_ndc
ndc	package	55118-530-12	openfda.package_ndc
ndc	package	55118-530-63	openfda.package_ndc
ndc	package	55118-530-92	openfda.package_ndc
ndc	product	55118-530	openfda.product_ndc
ndc11	package	55118053065	derived:openfda.package_ndc
ndc11	package	55118053010	derived:openfda.package_ndc
ndc11	package	55118053011	derived:openfda.package_ndc
ndc11	package	55118053099	derived:openfda.package_ndc
ndc11	package	55118053091	derived:openfda.package_ndc
ndc11	package	55118053063	derived:openfda.package_ndc
ndc11	package	55118053088	derived:openfda.package_ndc
ndc11	package	55118053012	derived:openfda.package_ndc
ndc11	package	55118053092	derived:openfda.package_ndc
rxcui		616805	openfda.rxcui
spl id		92ebe19a-e5cd-40cb-89ec-60d675a726d3	id
spl set id		75e884bf-8e0d-41e7-adbb-4400ee3d1e07	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 flame. Do not use on children less than 2 months of age or on open skin wounds When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if Irritation or rash occurs. 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.