Listerine Cool Mint Antiseptic

Dosage form: liquid
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: 69968-0550

Medically reviewed by Drugs.com. Last updated on Apr 10, 2025.

Listerine Cool Mint Antiseptic

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, Poloxamer 407, Benzoic Acid, Sodium Saccharin, Sodium Benzoate, Flavor, Green 3

Questions or Comments?

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

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

PRINCIPAL DISPLAY PANEL - 1.5 L Bottle Label

ANTISEPTIC
LISTERINE®
COOL MINT®

FOR A FRESHER &
CLEANER MOUTH THAN
BRUSHING ALONE

ADA
Accepted
American
Dental
Association ®

30040704

1.5L (1 Qt 1 Pt 2.7 fl oz)

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0550
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
Saccharin Sodium
Sodium Benzoate
Fd&C Green No. 3

Packaging
#	Item Code	Package Description
1	NDC:69968-0550-9	95 mL in 1 BOTTLE
2	NDC:69968-0550-2	250 mL in 1 BOTTLE
3	NDC:69968-0550-5	500 mL in 1 BOTTLE
4	NDC:69968-0550-1	946.353 mL in 1 BOTTLE
5	NDC:69968-0550-4	1419.529 mL in 1 BOTTLE
6	NDC:69968-0550-3	3700 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part356	12/03/2018

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 04/2020

Document Id: 4a82bdab-1ad8-4a80-bcf5-d1e5d6776fcc

Set id: 9e97e4f8-80c2-44e0-862c-0dfca392a436

Version: 3

Effective Time: 20200420

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

Listerine Cool Mint Antiseptic

Further information

See also:

Qulipta

Aimovig

Dupixent

Gemtesa

Ubrelvy

Nurtec ODT

Xeomin

Tazarotene topical

Topiramate

Dysport