Listerine Ultraclean Antiseptic Cool Mint

Dosage form: mouthwash
Ingredients: Eucalyptol 0.92mg in 1mL, Menthol, unspecified form 0.42mg in 1mL, Methyl salicylate 0.6mg in 1mL, Thymol 0.64mg in 1mL
Labeler: Johnson & Johnson Consumer Inc.
NDC code: 69968-0539

Medically reviewed by Drugs.com. Last updated on Apr 26, 2024.

Listerine Ultraclean Antiseptic
Cool Mint

Drug Facts

Active ingredients

Eucalyptol 0.092%
Menthol 0.042%
Methyl salicylate 0.060%
Thymol 0.064%

Purposes

Antiplaque/antigingivitis

Uses

helps prevent and reduce:

plaque
gingivitis

Warnings

Do not use in children under 12 years of age

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.

Directions

rinse full strength for 30 seconds with 20 ml (2/3 fluid ounce or 4 teaspoonfuls) morning and night
do not swallow

Other information

store at room temperature
cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

water, alcohol (21.6%), sorbitol, flavor, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, sodium saccharin, green 3

Questions?

call toll-free 888-222-0182 or 215-273-8755 (collect)

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

ANTISEPTIC
LISTERINE®
ULTRACLEAN

FOR UP TO A 3X
LONGER LASTING
CLEAN FEELING*

*vs. brushing alone

COOL MINT®

500 mL (1.05 Pt)

LISTERINE ULTRACLEAN ANTISEPTIC COOL MINT
eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0539
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Eucalyptol (Eucalyptol)	Eucalyptol	0.92 mg in 1 mL
Menthol, unspecified form (Menthol, unspecified form)	Menthol, unspecified form	0.42 mg in 1 mL
Methyl salicylate (Salicylic acid)	Methyl salicylate	0.6 mg in 1 mL
Thymol (Thymol)	Thymol	0.64 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Alcohol
Sorbitol
Poloxamer 407
Benzoic Acid
Zinc Chloride
Sodium Benzoate
Sucralose
Saccharin Sodium
FD&C GREEN NO. 3

Packaging
#	Item Code	Package Description
1	NDC:69968-0539-2	250 mL in 1 BOTTLE, PLASTIC
2	NDC:69968-0539-5	500 mL in 1 BOTTLE, PLASTIC
3	NDC:69968-0539-1	1000 mL in 1 BOTTLE, PLASTIC
4	NDC:69968-0539-3	1500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part356	06/01/2012

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 05/2020

Document Id: a66bee81-3573-4d0c-9dbb-06305048b511

Set id: dd3729c2-fd05-4db0-a542-487bb0f9001f

Version: 2

Effective Time: 20200506

Johnson & Johnson Consumer Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer