| Product NDC: | 21695-854 |
| Proprietary Name: | Miconazole Nitrate |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 21695-854 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080101 |
| Package NDC: | 21695-854-45 |
| Package Description: | 45 g in 1 TUBE (21695-854-45) |
| NDC Code | 21695-854-45 |
| Proprietary Name | Miconazole Nitrate |
| Package Description | 45 g in 1 TUBE (21695-854-45) |
| Product NDC | 21695-854 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 20080101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |