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 24, 2025.

LISTERINE GUM THERAPY ANTISEPTIC

Drug Facts

Active ingredient	Purpose
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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0604
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 BLUE NO. 1

Packaging
#	Item Code	Package Description
1	NDC:69968-0604-5	500 mL in 1 BOTTLE, PLASTIC
2	NDC:69968-0604-1	1000 mL in 1 BOTTLE, PLASTIC
3	NDC:69968-0604-9	95 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	01/06/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 04/2020

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

Listerine Gum Therapy Antiseptic

Further information

See also:

Rybelsus

Zepbound

Ozempic

Wegovy

Victoza

Saxenda

Alli

Methamphetamine

Amphetamine

Phentermine