Skip to main content

Listerine Gum Therapy Antiseptic

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: 69968-0604

Medically reviewed by Drugs.com. Last updated on Mar 25, 2024.

LISTERINE GUM THERAPY ANTISEPTIC

Drug Facts

Active ingredientPurpose
Eucalyptol (0.092%)Antiplaque/antigingivitis
Menthol (0.042%)Antiplaque/antigingivitis
Methyl Salicylate (0.060%)Antiplaque/antigingivitis
Thymol (0.064%)Antiplaque/antigingivitis

Use

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 20mL (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% v/v), Sorbitol, Poloxamer 407, Benzoic Acid, Zinc Chloride, Sodium Benzoate, Sucralose, Flavor, Sodium Saccharin, Blue 1

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 1.0 L Bottle Label

ANTISEPTIC
LISTERINE
GUM THERAPY
4X
HEALTHIER*

HELPS REVERSE SIGNS OF
EARLY GUM DISEASE: REDNESS,
BLEEDING AND INFLAMMATION

GLACIER MINT
1.0 L (1 Qt 1.8 Fl Oz)

LISTERINE GUM THERAPY ANTISEPTIC 
eucalyptol, menthol, unspecified form, methyl salicylate, and thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0604
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 
Zinc Chloride 
Sodium Benzoate 
Sucralose 
SACCHARIN SODIUM 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:69968-0604-5500 mL in 1 BOTTLE, PLASTIC
2NDC:69968-0604-11000 mL in 1 BOTTLE, PLASTIC
3NDC:69968-0604-995 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35601/06/2020
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Document Id: a7df3436-d381-4b4e-b146-9600a3ad6e5a
Set id: d9b146a4-1e3d-4aa8-856c-ab393b9570a4
Version: 2
Effective Time: 20200402
 
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