Kleenex Reveal Moisturizing Foam 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 Reveal Moisturizing Foam Hand Sanitizer
Generic name: ALCOHOL
Manufacturer: Kimberly-Clark
Product type: HUMAN OTC DRUG
SPL set ID: 4a491f90-268e-470d-a74c-473f1efe7c8b
SPL ID: 7518fc00-ed91-408b-80e2-8d9fc55ed77a
Version: 8
Effective date: 2026-05-06
Source export date: 2026-10-12
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:28:29

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		Kleenex Reveal Moisturizing Foam Hand Sanitizer	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Kimberly-Clark	openfda.manufacturer_name
ndc	package	55118-531-10	openfda.package_ndc
ndc	package	55118-531-18	openfda.package_ndc
ndc	package	55118-531-64	openfda.package_ndc
ndc	package	55118-531-11	openfda.package_ndc
ndc	package	55118-531-12	openfda.package_ndc
ndc	package	55118-531-67	openfda.package_ndc
ndc	product	55118-531	openfda.product_ndc
ndc11	package	55118053164	derived:openfda.package_ndc
ndc11	package	55118053112	derived:openfda.package_ndc
ndc11	package	55118053111	derived:openfda.package_ndc
ndc11	package	55118053167	derived:openfda.package_ndc
ndc11	package	55118053110	derived:openfda.package_ndc
ndc11	package	55118053118	derived:openfda.package_ndc
rxcui		616805	openfda.rxcui
spl id		7518fc00-ed91-408b-80e2-8d9fc55ed77a	id
spl set id		4a491f90-268e-470d-a74c-473f1efe7c8b	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.