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Listerine Antiseptic - 42002-401-72 - (Eucalyptol, Menthol, Methyl Salicylate, and Thymol)

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Drug Information of Listerine Antiseptic

Product NDC: 42002-401
Proprietary Name: Listerine Antiseptic
Non Proprietary Name: Eucalyptol, Menthol, Methyl Salicylate, and Thymol
Active Ingredient(s): .92; .42; .6; .64    mg/mL; mg/mL; mg/mL; mg/mL & nbsp;   Eucalyptol, Menthol, Methyl Salicylate, and Thymol
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Listerine Antiseptic

Product NDC: 42002-401
Labeler Name: Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120221

Package Information of Listerine Antiseptic

Package NDC: 42002-401-72
Package Description: 500 mL in 1 BOTTLE, PLASTIC (42002-401-72)

NDC Information of Listerine Antiseptic

NDC Code 42002-401-72
Proprietary Name Listerine Antiseptic
Package Description 500 mL in 1 BOTTLE, PLASTIC (42002-401-72)
Product NDC 42002-401
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Eucalyptol, Menthol, Methyl Salicylate, and Thymol
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 20120221
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Johnson & Johnson Healthcare Products, Division of McNEIL-PPC, Inc.
Substance Name EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Strength Number .92; .42; .6; .64
Strength Unit mg/mL; mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Listerine Antiseptic


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