Listerine Ultraclean Antiseptic description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Listerine Ultraclean Antiseptic

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

Listerine Ultraclean AntisepticFresh Citrus


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purposes
Eucalyptol 0.092%
Menthol 0.042%
Methyl salicylate 0.060% Antiplaque/antigingivitis
Thymol 0.064%

Listerine Ultraclean 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 Ultraclean Antiseptic Other information

  • store at controlled room temperature 20° - 25° C (68° – 77° F)
  • cold weather may cloud this product. Its antiseptic properties are not affected.

Inactive ingredients

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

Questions?

call toll-free 1-888-222-0182 or 215-273-8755 (collect)

Dist: Johnson & Johnson Healthcare Products
Division of McNEIL-PPC, Inc.
Skillman, NJ 08558-9418 USA

PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

LISTERINE®
ULTRACLEAN™

WITH EVERFRESH™ TECHNOLOGY

ANTISEPTIC

Controls Tartar Build-up
Kills Plaque 7 Gingivitis
Germs, Keeps Breath
Fresh for Hours

* vs. brushing alone                          FRESH CITRUS

500 mL (1.05 Pt)

Listerine Ultraclean Antiseptic

Listerine Ultraclean Antiseptic

Eucalyptol, Menthol, Methyl Salicylate, and Thymol MOUTHWASH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-449
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
SODIUM BENZOATE
Sucralose
FD&C YELLOW NO. 6
FD&C RED NO. 40

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42002-449-72 500 in 1 BOTTLE, PLASTIC
2 NDC:42002-449-71 1000 in 1 BOTTLE, PLASTIC
3 NDC:42002-449-70 1500 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2012-07-10


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.