LISTERINE CLINICAL SOLUTIONS GUM HEALTH ICY MINT- eucalyptol, menthol, methyl salicylate, thymol mouthwash 
Johnson & Johnson Consumer Inc.

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Listerine Clinical Solutions Gum Health Icy Mint

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

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

• this rinse is not intended to replace brushing or flossing

• store at room temperature

• cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

Water, Alcohol, Sorbitol, Poloxamer 407, Flavor, Zinc Chloride, Benzoic Acid, Sodium Benzoate, Sodium Saccharin, Sucralose, Red 40

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 L Bottle Label

ANTIGINGIVITIS / ANTIPLAQUE MOUTHWASH

LISTERINE ®

CLINICAL

SOLUTIONS

ANTISEPTIC

GUM HEALTH

Immediately kills the germs that cause

bleeding and inflammation for 3X healthier

gums in one week* (*vs. brushing alone)

ICY MINT

1L (1 Qt 1.8 Fl Oz)

Listerine_01

LISTERINE CLINICAL SOLUTIONS GUM HEALTH ICY MINT 
eucalyptol, menthol, methyl salicylate, thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0818
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL0.92 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.42 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 RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0818-995 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
2NDC:69968-0818-5500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
3NDC:69968-0818-11000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02210/16/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 10/2023
Document Id: 06e10b84-2988-febb-e063-6394a90a8ec8
Set id: 06e1122b-1100-43c0-e063-6394a90a2e78
Version: 1
Effective Time: 20231004
 
Johnson & Johnson Consumer Inc.