Panitrol - 59940-001-03 - (Menthol)

Alphabetical Index


Drug Information of Panitrol

Product NDC: 59940-001
Proprietary Name: Panitrol
Non Proprietary Name: Menthol
Active Ingredient(s): 4.25    g/85g & nbsp;   Menthol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Panitrol

Product NDC: 59940-001
Labeler Name: Enzyme Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101101

Package Information of Panitrol

Package NDC: 59940-001-03
Package Description: 85 g in 1 TUBE (59940-001-03)

NDC Information of Panitrol

NDC Code 59940-001-03
Proprietary Name Panitrol
Package Description 85 g in 1 TUBE (59940-001-03)
Product NDC 59940-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20101101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Enzyme Labs
Substance Name MENTHOL
Strength Number 4.25
Strength Unit g/85g
Pharmaceutical Classes

Complete Information of Panitrol


General Information