LISTERINE TOTAL CARE ZERO  FRESHMINT - sodium fluoride mouthwash 
Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

----------

Listerine® TOTAL CARE ZERO, Fresh Mint
Anticavity Mouthwash

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

• Adults and children 6 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 6 years of age: consult a dentist or doctor

Other information

• store at controlled room temperature 20° - 25°C (68° - 77°F)
• cold weather may temporarily cloud this product

Inactive ingredients

water, sorbitol solution, propylene glycol, flavors, sodium lauryl sulfate, poloxamer 407, sodium benzoate, phosphoric acid, sodium saccharin, disodium phosphate, sucralose, FD&C red no. 40, FD&C blue no.

Questions?

call 1-888-222-0182, weekdays

PRINCIPAL DISPLAY PANEL - 250 mL Bottle Label

LISTERINE®
TOTAL CARE
ZERO™
ANTICAVITY MOUTHWASH

SODIUM FLUORIDE & ACIDULATED PHOSPHATE TOPICAL SOLUTION

6
BENEFITS
IN 1

• Helps Prevent Cavities
• Restores Enamel
• Strengthens Teeth
• Kills Bad Breath Germs
• Cleans the Whole Mouth
• Alcohol Free

FRESH MINT

500 mL (1.05 pt)

IMPORTANT: Read directions
for proper use.

LISTERINE TOTAL CARE ZERO   FRESHMINT sodium fluoride   mouthwash

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 42002-443 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Fluoride (Fluoride Ion) Sodium Fluoride 0.221 g  in 1 mL

Inactive Ingredients Ingredient Name Strength Water   Sorbitol   Propylene Glycol   Sodium Lauryl Sulfate   Poloxamer 407   Sodium Benzoate   Phosphoric Acid   Saccharin Sodium   Sucralose   FD&C Red No. 40   FD&C Blue No. 1

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 42002-443-95 95 mL In 1 BOTTLE, PLASTIC None 2 42002-443-73 250 mL In 1 BOTTLE, PLASTIC None 3 42002-443-72 500 mL In 1 BOTTLE, PLASTIC None 4 42002-443-71 1000 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	05/01/2011

Labeler - Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. (831417154)

Revised: 03/2011Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.