LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - BERRY SPLASH- sodium fluoride mouthwash 
Johnson & Johnson Consumer Inc.

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LISTERINE ® SMART RINSE ® ANTICAVITY FLUORIDE RINSE BERRY SPLASH

Drug Facts

Active ingredient

Sodium fluoride 0.02% (0.01% w/v fluoride ion)

Purpose

Anticavity

Use

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

Other information

Inactive ingredients

Water, Sorbitol, Flavor, Phosphoric Acid, Cetylpyridinium Chloride, Sucralose, Sodium Saccharin, Disodium Phosphate, Red 33, Green 3

Questions?

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

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

2X STRONGER TEETH FOR

BETTER CAVITY PROTECTION*

*with brushing, in a lab study.

ALCOHOL FREE


ANTICAVITY FLUORIDE RINSE

LISTERINE ®

SMART RiNSE ®

SODIUM FLUORIDE & ACIDULATED PHOSPAHTE TOPICAL SOLUTION

BERRY

SPLASH

500 mL (16.9Fl Oz)

IMPORTANT: Read

directions for proper use.

Berry Splash

LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - BERRY SPLASH 
sodium fluoride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0687
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
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0687-5500 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02101/01/2021
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 4/2024
Document Id: 15180792-a3ac-2f3b-e063-6394a90a403f
Set id: ee9a962d-83c7-4b13-bff6-140e48785e8a
Version: 3
Effective Time: 20240402
 
Johnson & Johnson Consumer Inc.