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Soft Mint Listerine - 42002-404-73 - (Eucalyptol, Menthol, Methyl Salicylate and Thymol)

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Drug Information of Soft Mint Listerine

Product NDC: 42002-404
Proprietary Name: Soft Mint Listerine
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): DENTAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Soft Mint Listerine

Product NDC: 42002-404
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: 20100205

Package Information of Soft Mint Listerine

Package NDC: 42002-404-73
Package Description: 250 mL in 1 BOTTLE, PLASTIC (42002-404-73)

NDC Information of Soft Mint Listerine

NDC Code 42002-404-73
Proprietary Name Soft Mint Listerine
Package Description 250 mL in 1 BOTTLE, PLASTIC (42002-404-73)
Product NDC 42002-404
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Eucalyptol, Menthol, Methyl Salicylate and Thymol
Dosage Form Name MOUTHWASH
Route Name DENTAL
Start Marketing Date 20100205
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 Soft Mint Listerine


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