KINeSYS - 61481-0020-1 - (METHYL SALICYLATE and MENTHOL)

Alphabetical Index


Drug Information of KINeSYS

Product NDC: 61481-0020
Proprietary Name: KINeSYS
Non Proprietary Name: METHYL SALICYLATE and MENTHOL
Active Ingredient(s): 15; 30    g/100g; g/100g & nbsp;   METHYL SALICYLATE and MENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): STICK
Coding System: National Drug Codes(NDC)

Labeler Information of KINeSYS

Product NDC: 61481-0020
Labeler Name: KINeSYS Pharmaceutical Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120531

Package Information of KINeSYS

Package NDC: 61481-0020-1
Package Description: 50 g in 1 CYLINDER (61481-0020-1)

NDC Information of KINeSYS

NDC Code 61481-0020-1
Proprietary Name KINeSYS
Package Description 50 g in 1 CYLINDER (61481-0020-1)
Product NDC 61481-0020
Product Type Name HUMAN OTC DRUG
Non Proprietary Name METHYL SALICYLATE and MENTHOL
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20120531
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name KINeSYS Pharmaceutical Inc.
Substance Name MENTHOL; METHYL SALICYLATE
Strength Number 15; 30
Strength Unit g/100g; g/100g
Pharmaceutical Classes

Complete Information of KINeSYS


General Information