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