LISTERINE GUM THERAPY GLACIER MINT- eucalyptol, menthol, methyl salicylate, thymol mouthwash 
Johnson & Johnson Consumer Inc.

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Listerine Gum Therapy Mouthwash

Glacier Mint

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:

Warnings

Do not use in children under 12 years of age

Ask a dentist if symptoms persist, new symptoms appear, or conditions worsen after regular use

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

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

ANTIGINGIVITIS / ANTIPLAQUE MOUTHWASH

LISTERINE ®

GUM THERAPY

4X

HEALTHIER*

HELPS REVERSE SIGNS OF

EARLY GUM DISEASE: REDNESS,

BLEEDING & INFLAMMATION

GLACIER MINT

1.0 L (1 Qt 1.8 Fl Oz)

Listerine_01

LISTERINE GUM THERAPY  GLACIER MINT
eucalyptol, menthol, methyl salicylate, thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0790
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL0.92 mg  in 1 mL
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM0.42 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.6 mg  in 1 mL
THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL0.64 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
SORBITOL (UNII: 506T60A25R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0790-5500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/2023
2NDC:69968-0790-11000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/2023
3NDC:69968-0790-995 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/13/2023
4NDC:69968-0790-21500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2023
5NDC:69968-0790-32 in 1 TRAY03/01/2024
51500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02202/13/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 2/2024
Document Id: 11e07a74-ee00-2bdf-e063-6394a90ac26c
Set id: ed6889b6-58db-41cf-e053-2a95a90a7de2
Version: 4
Effective Time: 20240221
 
Johnson & Johnson Consumer Inc.