Soft Mint Listerine description, usages, side effects, indications, overdosage, supplying and lots more!

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Soft Mint Listerine

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

Soft Mint Listerine Antiseptic [250 ml, 500 ml, 1 L, 1.5 L]


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

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

Soft Mint Listerine 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

Soft Mint Listerine 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, poloxamer 407, flavor, benzoic acid, sucralose, sodium benzoate, propylene glycol alginate, FD&C yellow no. 6, FD&C blue no. 1

Questions?

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

PRINCIPAL DISPLAY PANEL - 1.5 Liter Bottle Label

LISTERINE®
SOFT MINT®

ANTISEPTIC

Kills Germs that Cause
Bad Breath, Plaque & the
Gum Disease Gingivitis

ADA
Accepted
American
Dental Association

1.5L (1 Qt 1 Pt 2.7 Fl OZ)

Soft Mint Listerine

Soft Mint Listerine

Eucalyptol, Menthol, Methyl Salicylate and Thymol MOUTHWASH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42002-404
Route of Administration DENTAL 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
Sucralose
SODIUM BENZOATE
PROPYLENE GLYCOL ALGINATE
FD&C YELLOW NO. 6
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42002-404-73 250 in 1 BOTTLE, PLASTIC
2 NDC:42002-404-72 500 in 1 BOTTLE, PLASTIC
3 NDC:42002-404-71 1000 in 1 BOTTLE, PLASTIC
4 NDC:42002-404-70 1500 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2010-02-05


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Be sure to consult your doctor before taking any medication!
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