NDC 69968-0550

Listerine Cool Mint Antiseptic

Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol

Listerine Cool Mint Antiseptic is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is Eucalyptol; Menthol, Unspecified Form; Methyl Salicylate; Thymol.

Product ID69968-0550_2914bfa2-dd0f-4e30-bd12-0ee87b37bc14
NDC69968-0550
Product TypeHuman Otc Drug
Proprietary NameListerine Cool Mint Antiseptic
Generic NameEucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2018-12-03
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart356
Labeler NameJohnson & Johnson Consumer Inc.
Substance NameEUCALYPTOL; MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE; THYMOL
Active Ingredient Strength1 mg/mL; mg/mL; mg/mL; mg/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 69968-0550-1

946.353 mL in 1 BOTTLE (69968-0550-1)
Marketing Start Date2018-12-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69968-0550-9 [69968055009]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-03

NDC 69968-0550-3 [69968055003]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-01

NDC 69968-0550-5 [69968055005]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-03

NDC 69968-0550-4 [69968055004]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-03

NDC 69968-0550-2 [69968055002]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-03

NDC 69968-0550-1 [69968055001]

Listerine Cool Mint Antiseptic LIQUID
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart356
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-03

Drug Details

Active Ingredients

IngredientStrength
EUCALYPTOL.92 mg/mL

OpenFDA Data

SPL SET ID:9e97e4f8-80c2-44e0-862c-0dfca392a436
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1043623
  • 1043619
  • UPC Code
  • 0312547427555
  • NDC Crossover Matching brand name "Listerine Cool Mint Antiseptic" or generic name "Eucalyptol, Menthol, Unspecified Form, Methyl Salicylate, And Thymol"

    NDCBrand NameGeneric Name
    42002-402Listerine Cool Mint AntisepticEucalyptol, Menthol, Methyl Salicylate, and Thymol
    69968-0477Listerine Cool Mint AntisepticEucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol
    69968-0550Listerine Cool Mint AntisepticEucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
    66715-6861AntisepticEucalyptol, Menthol, Unspecified Form, Methyl salicylate, and Thymol
    69968-0400LISTERINEEucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
    69968-0239Listerine FreshBurst AntisepticEucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol
    69968-0604Listerine Gum Therapy Antisepticeucalyptol, menthol, unspecified form, methyl salicylate, and thymol
    69968-0539Listerine Ultraclean AntisepticEucalyptol, Menthol, unspecified form, Methyl Salicylate, and Thymol
    69968-0399Listerine Ultraclean Arctic MintEucalyptol, Menthol, Unspecified Form, Methyl Salicylate, and Thymol
    69968-0398Listerine Ultraclean Fresh CitrusEucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol

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