| Product NDC: | 63736-015 |
| Proprietary Name: | Monistat 3 |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 40 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-015 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020827 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980330 |
| Package NDC: | 63736-015-18 |
| Package Description: | 3 TUBE, WITH APPLICATOR in 1 CARTON (63736-015-18) > 5 g in 1 TUBE, WITH APPLICATOR |
| NDC Code | 63736-015-18 |
| Proprietary Name | Monistat 3 |
| Package Description | 3 TUBE, WITH APPLICATOR in 1 CARTON (63736-015-18) > 5 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 63736-015 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 19980330 |
| Marketing Category Name | NDA |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 40 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |