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Soft Mint Listerine Antiseptic

Dosage form: mouthwash
Ingredients: Eucalyptol 0.92mg in 1mL, Menthol 0.42mg in 1mL, Methyl Salicylate 0.6mg in 1mL, Thymol 0.64mg in 1mL
Labeler: Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
NDC Code: 42002-404

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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

Drug Facts

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


helps prevent and reduce:

  • plaque
  • gingivitis


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.

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

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


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

PRINCIPAL DISPLAY PANEL - 1.5 Liter Bottle Label



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

Dental Association

1.5L (1 Qt 1 Pt 2.7 Fl OZ)

eucalyptol, menthol, methyl salicylate and thymol mouthwash
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42002-404
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Eucalyptol (Eucalyptol) Eucalyptol0.92 mg  in 1 mL
Menthol (Menthol) Menthol0.42 mg  in 1 mL
Methyl Salicylate (Salicylic Acid) Methyl Salicylate0.6 mg  in 1 mL
Thymol (Thymol) Thymol0.64 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Poloxamer 407 
Benzoic Acid 
Sodium Benzoate 
Propylene Glycol Alginate 
FD&C Yellow No. 6 
FD&C Blue No. 1 
#Item CodePackage Description
1NDC:42002-404-73250 mL in 1 BOTTLE, PLASTIC
2NDC:42002-404-72500 mL in 1 BOTTLE, PLASTIC
3NDC:42002-404-711000 mL in 1 BOTTLE, PLASTIC
4NDC:42002-404-701500 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35602/05/2010
Labeler - Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc. (831417154)

Revised: 11/2012
Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.