MOLYHEN - 50629-1010-2 - (MENTHOL)

Alphabetical Index


Drug Information of MOLYHEN

Product NDC: 50629-1010
Proprietary Name: MOLYHEN
Non Proprietary Name: MENTHOL
Active Ingredient(s): 2; 4; 2; 10    mL/200mL; mL/200mL; mL/200mL; mL/200mL & nbsp;   MENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of MOLYHEN

Product NDC: 50629-1010
Labeler Name: SEWHA P&C INC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110629

Package Information of MOLYHEN

Package NDC: 50629-1010-2
Package Description: 1 BOTTLE in 1 BOX (50629-1010-2) > 200 mL in 1 BOTTLE (50629-1010-1)

NDC Information of MOLYHEN

NDC Code 50629-1010-2
Proprietary Name MOLYHEN
Package Description 1 BOTTLE in 1 BOX (50629-1010-2) > 200 mL in 1 BOTTLE (50629-1010-1)
Product NDC 50629-1010
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MENTHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110629
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name SEWHA P&C INC
Substance Name .ALPHA.-TOCOPHEROL ACETATE, D-; MENTHOL; PYRIDOXINE HYDROCHLORIDE; SWERTIA JAPONICA
Strength Number 2; 4; 2; 10
Strength Unit mL/200mL; mL/200mL; mL/200mL; mL/200mL
Pharmaceutical Classes

Complete Information of MOLYHEN


General Information