LISTERINE CLINICAL SOLUTIONS TEETH STRENGTH ALPINE MINT- sodium fluoride mouthwash 
Johnson & Johnson Consumer Inc.

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Listerine Clinical Solutions Teeth Strength Alpine Mint

Drug Facts

Active ingredient

Sodium Fluoride 0.02% (0.01% w/v Fluoride Ion)

Purpose

Anticavity

Uses

aids in the prevention of dental cavities

Warnings

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

Adults and children 12 years of age and older:

Children under 12 years of age: consult a dentist or a doctor

Other information

Inactive ingredients

Water, Alcohol, Sorbitol, Poloxamer 407, Flavor, Sodium Lauryl Sulfate, Eucalyptol, Sodium Saccharin, Methyl Salicylate, Thymol, Phosphoric Acid, Menthol, Sucralose, Disodium Phosphate, Green 3, Yellow 10

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

ANTICAVITY FLUORIDE MOUTHWASH

LISTERINE®

CLINICAL

SOLUTIONS

IMPORTANT: READ DIRECTIONS FOR PROPER USE

SODIUM FLUORIDE & ACIDULATED PHOSPHATE TOPICAL SOLUTION

TEETH STRENGTH

Repairs enamel now to prevent cavities

for 3X stronger* and longer-lasting teeth

(*with brushing in a lab study)

ALPINE MINT

1L (1 Qt 1.8 Fl Oz)

Listerine_01

LISTERINE CLINICAL SOLUTIONS TEETH STRENGTH ALPINE MINT 
sodium fluoride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0819
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
SORBITOL (UNII: 506T60A25R)  
POLOXAMER 407 (UNII: TUF2IVW3M2)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
WATER (UNII: 059QF0KO0R)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
EUCALYPTOL (UNII: RV6J6604TK)  
MENTHOL (UNII: L7T10EIP3A)  
METHYL SALICYLATE (UNII: LAV5U5022Y)  
THYMOL (UNII: 3J50XA376E)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0819-995 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
2NDC:69968-0819-5500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
3NDC:69968-0819-11000 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 DrugM02110/16/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 2/2024
Document Id: 11e66b6c-747a-60fd-e063-6394a90a32ea
Set id: 06e2de03-4a58-3de0-e063-6294a90a5857
Version: 2
Effective Time: 20240221
 
Johnson & Johnson Consumer Inc.