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Listerine Cool Mint Antiseptic

Medically reviewed by Drugs.com. Last updated on April 20, 2020.

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

Further information

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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0550
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Eucalyptol (Eucalyptol) Eucalyptol0.92 mg  in 1 mL
Menthol, Unspecified Form (Menthol, Unspecified Form) Menthol, Unspecified Form0.42 mg  in 1 mL
Methyl Salicylate (Salicylic Acid) Methyl Salicylate0.6 mg  in 1 mL
Thymol (Thymol) Thymol0.64 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water 
Alcohol 
Sorbitol 
Poloxamer 407 
Benzoic Acid 
Saccharin Sodium 
Sodium Benzoate 
Fd&C Green No. 3 
Packaging
#Item CodePackage Description
1NDC:69968-0550-995 mL in 1 BOTTLE
2NDC:69968-0550-2250 mL in 1 BOTTLE
3NDC:69968-0550-5500 mL in 1 BOTTLE
4NDC:69968-0550-1946.353 mL in 1 BOTTLE
5NDC:69968-0550-41419.529 mL in 1 BOTTLE
6NDC:69968-0550-33700 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35612/03/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Document Id: 4a82bdab-1ad8-4a80-bcf5-d1e5d6776fcc
Set id: 9e97e4f8-80c2-44e0-862c-0dfca392a436
Version: 3
Effective Time: 20200420
 
Johnson & Johnson Consumer Inc.

Medical Disclaimer