Listerine Total Care Zero description, usages, side effects, indications, overdosage, supplying and lots more!

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Listerine Total Care Zero

Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Listerine® TOTAL CARE ZERO, Fresh Mint Anticavity Mouthwash


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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

Listerine Total Care Zero 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

Listerine Total Care Zero

Sodium Fluoride MOUTHWASH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-443
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.221 g

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
propylene glycol
SODIUM LAURYL SULFATE
POLOXAMER 407
SODIUM BENZOATE
phosphoric acid
SACCHARIN SODIUM DIHYDRATE
Sucralose
FD&C RED NO. 40
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42002-443-95 95 in 1 BOTTLE, PLASTIC
2 NDC:42002-443-73 250 in 1 BOTTLE, PLASTIC
3 NDC:42002-443-72 500 in 1 BOTTLE, PLASTIC
4 NDC:42002-443-71 1000 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2011-05-01


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Be sure to consult your doctor before taking any medication!
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