Home
>
National Drug Code (NDC)
>
footlogix
footlogix - 42479-212-17 - (Clotrimazole)
Drug Information of footlogix
| Product NDC: | 42479-212 |
| Proprietary Name: | footlogix |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 1 mL/100mL & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of footlogix
| Product NDC: | 42479-212 |
| Labeler Name: | KVG Group Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of footlogix
| Package NDC: | 42479-212-17 |
| Package Description: | 50 mL in 1 CAN (42479-212-17) |
NDC Information of footlogix
| NDC Code | 42479-212-17 |
| Proprietary Name | footlogix |
| Package Description | 50 mL in 1 CAN (42479-212-17) |
| Product NDC | 42479-212 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KVG Group Inc |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 1 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
