LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - BUBBLE BLAST- sodium fluoride mouthwash 
Johnson & Johnson Consumer Inc.

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LISTERINE ® SMART RINSE ® ANTICAVITY FLUORIDE RINSE BUBBLE BLAST

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, Sucralose, Cetylpyridinium Chloride, Disodium Phosphate, Sodium Saccharin, Menthol, Blue , 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

BUBBLE

BLAST

500 mL (16.9Fl Oz)

IMPORTANT: Read

directions for proper use.

Bubble Blast

LISTERINE SMART RINSE ANTICAVITY FLUORIDE RINSE - BUBBLE BLAST 
sodium fluoride mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0690
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)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0690-5500 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: 15187b80-c88e-5832-e063-6394a90a70b9
Set id: f09f334b-709c-473e-b91e-3f31480ceb90
Version: 3
Effective Time: 20240402
 
Johnson & Johnson Consumer Inc.