LISTERINE - 42002-421-71 - (Sodium fluoride)

Alphabetical Index


Drug Information of LISTERINE

Product NDC: 42002-421
Proprietary Name: LISTERINE
Non Proprietary Name: Sodium fluoride
Active Ingredient(s): 2.21    mg/10mL & nbsp;   Sodium fluoride
Administration Route(s): DENTAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of LISTERINE

Product NDC: 42002-421
Labeler Name: Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091130

Package Information of LISTERINE

Package NDC: 42002-421-71
Package Description: 1000 mL in 1 BOTTLE, PLASTIC (42002-421-71)

NDC Information of LISTERINE

NDC Code 42002-421-71
Proprietary Name LISTERINE
Package Description 1000 mL in 1 BOTTLE, PLASTIC (42002-421-71)
Product NDC 42002-421
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium fluoride
Dosage Form Name MOUTHWASH
Route Name DENTAL
Start Marketing Date 20091130
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance Name SODIUM FLUORIDE
Strength Number 2.21
Strength Unit mg/10mL
Pharmaceutical Classes

Complete Information of LISTERINE


General Information