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Nail MD
Nail MD - 55992-711-01 - (Miconazole Nitrate)
Drug Information of Nail MD
| Product NDC: | 55992-711 |
| Proprietary Name: | Nail MD |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 200 mg/mg & nbsp; Miconazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nail MD
| Product NDC: | 55992-711 |
| Labeler Name: | OMG Medical Group, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130214 |
Package Information of Nail MD
| Package NDC: | 55992-711-01 |
| Package Description: | 200 mg in 1 PACKAGE (55992-711-01) |
NDC Information of Nail MD
| NDC Code | 55992-711-01 |
| Proprietary Name | Nail MD |
| Package Description | 200 mg in 1 PACKAGE (55992-711-01) |
| Product NDC | 55992-711 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130214 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OMG Medical Group, LLC |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 200 |
| Strength Unit | mg/mg |
| Pharmaceutical Classes |
