NDC 42002-404

Soft Mint Listerine Antiseptic

Eucalyptol, Menthol, Methyl Salicylate And Thymol

Soft Mint Listerine Antiseptic is a Dental Mouthwash in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Healthcare Products, Division Of Mcneil-ppc, Inc.. The primary component is Eucalyptol; Menthol; Methyl Salicylate; Thymol.

Product ID42002-404_b225cc1a-bdb6-445f-a28d-bc1d8c67f8a8
NDC42002-404
Product TypeHuman Otc Drug
Proprietary NameSoft Mint Listerine Antiseptic
Generic NameEucalyptol, Menthol, Methyl Salicylate And Thymol
Dosage FormMouthwash
Route of AdministrationDENTAL
Marketing Start Date2010-02-05
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameJohnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance NameEUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Active Ingredient Strength1 mg/mL; mg/mL; mg/mL; mg/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 42002-404-72

500 mL in 1 BOTTLE, PLASTIC (42002-404-72)
Marketing Start Date2010-02-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42002-404-71 [42002040471]

Soft Mint Listerine Antiseptic MOUTHWASH
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-05
Marketing End Date2016-05-19

NDC 42002-404-70 [42002040470]

Soft Mint Listerine Antiseptic MOUTHWASH
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-05
Marketing End Date2018-11-17

NDC 42002-404-73 [42002040473]

Soft Mint Listerine Antiseptic MOUTHWASH
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-05
Marketing End Date2011-12-26

NDC 42002-404-72 [42002040472]

Soft Mint Listerine Antiseptic MOUTHWASH
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-05
Marketing End Date2014-04-20

Drug Details

Active Ingredients

IngredientStrength
EUCALYPTOL.92 mg/mL

OpenFDA Data

SPL SET ID:9509e548-3a0b-421e-a87d-a7af0f9438a6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1043623
  • 1043619
  • UPC Code
  • 0312547521550

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.