Listerine Advanced with Tartar Protection Antiseptic description, usages, side effects, indications, overdosage, supplying and lots more!

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Listerine Advanced with Tartar Protection Antiseptic

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

Advanced Listerine Antiseptic With Tartar Protection - Citrus -


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients

Eucalyptol 0.092%
Menthol 0.042%
Methyl salicylate 0.060%
Thymol 0.064%

Purposes

Antiplaque/antigingivitis

Listerine Advanced with Tartar Protection Antiseptic Uses

helps prevent and reduce:

  • plaque
  • gingivitis

Warnings

Do not use in children under 12 years of age

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

  • rinse full strength for 30 seconds with 20 ml (2/3 fluid ounce or 4 teaspoonfuls) morning and night
  • do not swallow

Listerine Advanced with Tartar Protection Antiseptic Other information

  • store at room temperature
  • cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

water, alcohol (21.6%), sorbitol solution, flavoring, poloxamer 407, benzoic acid, zinc chloride, sucralose, sodium benzoate, FD&C yellow no. 6, FD&C red no. 40.

Questions?

call 1-888-222-0182, weekdays or 215-273-8755 (collect)

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

LISTERINE ®
ADVANCED
WITH TARTAR PROTECTION

ANTISEPTIC

Kills the Germs that Cause
Bad Breath, Plaque & Gingivitis
Plus Prevents Tartar for a
Cleaner Mouth**

Citrus

500 mL (1.05 Pt)

Listerine Advanced with Tartar Protection Antiseptic

Listerine Advanced with Tartar Protection Antiseptic

Eucalyptol, Menthol, Methyl Salicylate, and Thymol MOUTHWASH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-407
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
EUCALYPTOL EUCALYPTOL 0.92 mg
MENTHOL 0.42 mg
methyl salicylate METHYL SALICYLATE 0.6 mg
THYMOL THYMOL 0.64 mg

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
sorbitol
POLOXAMER 407
BENZOIC ACID
ZINC CHLORIDE
Sucralose
SODIUM BENZOATE
FD&C YELLOW NO. 6
FD&C RED NO. 40

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42002-407-95 95 in 1 BOTTLE, PLASTIC
2 NDC:42002-407-73 250 in 1 BOTTLE, PLASTIC
3 NDC:42002-407-72 500 in 1 BOTTLE, PLASTIC
4 NDC:42002-407-71 1000 in 1 BOTTLE, PLASTIC
5 NDC:42002-407-70 1500 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2013-10-11


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