Mediflex - 67662-001-03 - (Menthol)

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Drug Information of Mediflex

Product NDC: 67662-001
Proprietary Name: Mediflex
Non Proprietary Name: Menthol
Active Ingredient(s): 5    1/85g & nbsp;   Menthol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Mediflex

Product NDC: 67662-001
Labeler Name: SAS Group Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100329

Package Information of Mediflex

Package NDC: 67662-001-03
Package Description: 85 g in 1 JAR (67662-001-03)

NDC Information of Mediflex

NDC Code 67662-001-03
Proprietary Name Mediflex
Package Description 85 g in 1 JAR (67662-001-03)
Product NDC 67662-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100329
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name SAS Group Inc.
Substance Name MENTHOL
Strength Number 5
Strength Unit 1/85g
Pharmaceutical Classes

Complete Information of Mediflex


General Information