Listerine FreshBurst Antiseptic

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 FreshBurst Antiseptic
Generic name: EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: 62b5c3ee-01cc-4c4e-9f28-e7dafa7372d8
SPL ID: 22634de5-9318-1b56-e063-6394a90a6245
Version: 9
Effective date: 2024-11-11
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:55:41

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 FreshBurst Antiseptic	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	69968-0239-1	openfda.package_ndc
ndc	package	69968-0239-3	openfda.package_ndc
ndc	package	69968-0239-8	openfda.package_ndc
ndc	package	69968-0239-5	openfda.package_ndc
ndc	package	69968-0239-2	openfda.package_ndc
ndc	product	69968-0239	openfda.product_ndc
ndc11	package	69968023905	derived:openfda.package_ndc
ndc11	package	69968023908	derived:openfda.package_ndc
ndc11	package	69968023903	derived:openfda.package_ndc
ndc11	package	69968023902	derived:openfda.package_ndc
ndc11	package	69968023901	derived:openfda.package_ndc
rxcui		1043623	openfda.rxcui
rxcui		1043619	openfda.rxcui
spl id		22634de5-9318-1b56-e063-6394a90a6245	id
spl set id		62b5c3ee-01cc-4c4e-9f28-e7dafa7372d8	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 Ask a dentist if symptoms persist , new symptoms appear, or conditions worsen after regular use Keep out of reach of children. 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.