| Product NDC: | 68754-150 |
| Proprietary Name: | Medicated Anti-Fungal Miconazole |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 2 g/100g & nbsp; Miconazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68754-150 |
| Labeler Name: | American Spraytech, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100602 |
| Package NDC: | 68754-150-00 |
| Package Description: | 150 g in 1 CAN (68754-150-00) |
| NDC Code | 68754-150-00 |
| Proprietary Name | Medicated Anti-Fungal Miconazole |
| Package Description | 150 g in 1 CAN (68754-150-00) |
| Product NDC | 68754-150 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100602 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | American Spraytech, LLC |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |