Listerine HealthyWhite Anticavity Mouthrinse Vibrant - Clean Mint

Dosage form: mouthwash
Ingredients: Sodium Fluoride 0.1mg in 1mL
Labeler: Johnson & Johnson Consumer Inc.
NDC code: 42002-514

Medically reviewed by Drugs.com. Last updated on Sep 2, 2024.

LISTERINE® HealthyWhite™ VIBRANT CLEAN MINT

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

Stop use and ask a dentist if oral irritation or tooth sensitivity occurs

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:
- use twice daily after brushing your teeth with a toothpaste
- vigorously swish 10 mL (2 teaspoonfuls) of rinse between your teeth for 1 minute and then spit out
- do not swallow the rinse
- do not eat or drink for 30 minutes after rinsing
- supervise children as necessary until capable of using without supervision
Children under 12 years if age: consult a dentist or doctor

Other information

store at room temperature

Inactive ingredients

water, alcohol (8%), hydrogen peroxide, poloxamer 407, sodium saccharin, sucralose, menthol, phosphoric acid, disodium phosphate, flavor

Questions?

call toll-free 888-222-5545 or 215-273-8755 (collect)

Distributed by:
Johnson & Johnson Healthcare Products
Division of McNeil-PPC, Inc. Skillman,
NJ 08558-9418 USA

PRINCIPAL DISPLAY PANEL - 946 mL Bottle Label

LISTERINE®
HealthyWhite™

anticavity flouride mouthwash
SODIUM FLUORIDE & ACIDULATED PHOSPHATE TOPICAL SOLUTION

VIBRANT

Starts to Whiten on Contact
Enamel Safe
Kills Bad Breath Germs

CLEAN MINT

946 mL (32 Fl OZ)

IMPORTANT: READ DIRECTIONS FOR PROPER USE.
DO NOT USE IF PRINTED LISTERINE® BAND AROUND CAP IS BROKEN OR MISSING.

LISTERINE HEALTHYWHITE ANTICAVITY MOUTHRINSE VIBRANT - CLEAN MINT
sodium fluoride mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:42002-514
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Fluoride (Fluoride Ion)	Fluoride Ion	0.1 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water
Alcohol
Hydrogen Peroxide
Poloxamer 407
Saccharin Sodium
Sucralose
Menthol, Unspecified Form
Phosphoric Acid
Sodium Phosphate, Dibasic, Anhydrous

Packaging
#	Item Code	Package Description
1	NDC:42002-514-16	473 mL in 1 BOTTLE, PLASTIC
2	NDC:42002-514-32	946 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part355	12/01/2013	01/14/2021

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 09/2020

Document Id: 313b339c-66e3-49db-90ab-0bbe5703e64f

Set id: b7870833-d120-4fe0-9480-e804a8a44238

Version: 4

Effective Time: 20200911

Johnson & Johnson Consumer Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer