| Product NDC: | 68345-816 |
| Proprietary Name: | Select Medical Products Antifungal |
| Non Proprietary Name: | MICONAZOLE NITRATE |
| Active Ingredient(s): | 20 mg/g & nbsp; MICONAZOLE NITRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68345-816 |
| Labeler Name: | PSS WORLD MEDICAL, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
| Package NDC: | 68345-816-25 |
| Package Description: | 142 g in 1 TUBE (68345-816-25) |
| NDC Code | 68345-816-25 |
| Proprietary Name | Select Medical Products Antifungal |
| Package Description | 142 g in 1 TUBE (68345-816-25) |
| Product NDC | 68345-816 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MICONAZOLE NITRATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PSS WORLD MEDICAL, INC. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |