Listerine Ultraclean Antiseptic Cool Mint

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: Listerine Ultraclean Antiseptic Cool Mint
Generic name: EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: dd3729c2-fd05-4db0-a542-487bb0f9001f
SPL ID: 22797442-320d-5c9c-e063-6394a90a20c8
Version: 10
Effective date: 2024-11-11
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:10

Harmonized routes table
Harmonized routes
ORAL

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		Listerine Ultraclean Antiseptic Cool Mint	openfda.brand_name
generic name		EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0539-5	openfda.package_ndc
ndc	package	69968-0539-3	openfda.package_ndc
ndc	package	69968-0539-4	openfda.package_ndc
ndc	package	69968-0539-1	openfda.package_ndc
ndc	package	69968-0539-2	openfda.package_ndc
ndc	product	69968-0539	openfda.product_ndc
ndc11	package	69968053903	derived:openfda.package_ndc
ndc11	package	69968053901	derived:openfda.package_ndc
ndc11	package	69968053904	derived:openfda.package_ndc
ndc11	package	69968053902	derived:openfda.package_ndc
ndc11	package	69968053905	derived:openfda.package_ndc
rxcui		2043303	openfda.rxcui
rxcui		1043619	openfda.rxcui
spl id		22797442-320d-5c9c-e063-6394a90a20c8	id
spl set id		dd3729c2-fd05-4db0-a542-487bb0f9001f	set_id
unii		3J50XA376E	openfda.unii
unii		L7T10EIP3A	openfda.unii
unii		RV6J6604TK	openfda.unii
unii		LAV5U5022Y	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 Do not use in children under 12 years of age Ask a dentist if symptoms persist , new symptoms appear, or conditions worsen after regular use Keep out of reach of children . If more than used for rinsing is accidentally 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.