 
                        | 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 |