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PRO-EX
PRO-EX - 67234-014-01 - (Clotrimazole)
Drug Information of PRO-EX
| Product NDC: | 67234-014 |
| Proprietary Name: | PRO-EX |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | .01 g/g & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRO-EX
| Product NDC: | 67234-014 |
| Labeler Name: | Natureplex, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080122 |
Package Information of PRO-EX
| Package NDC: | 67234-014-01 |
| Package Description: | 42 g in 1 TUBE (67234-014-01) |
NDC Information of PRO-EX
| NDC Code | 67234-014-01 |
| Proprietary Name | PRO-EX |
| Package Description | 42 g in 1 TUBE (67234-014-01) |
| Product NDC | 67234-014 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080122 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Natureplex, LLC |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | .01 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
