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Flexitol Medicated Foot
Flexitol Medicated Foot - 43251-3340-1 - (Tolnaftate)
Drug Information of Flexitol Medicated Foot
| Product NDC: | 43251-3340 |
| Proprietary Name: | Flexitol Medicated Foot |
| Non Proprietary Name: | Tolnaftate |
| Active Ingredient(s): | 1 g/100g & nbsp; Tolnaftate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flexitol Medicated Foot
| Product NDC: | 43251-3340 |
| Labeler Name: | LaCorium Health International Pty Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120811 |
Package Information of Flexitol Medicated Foot
| Package NDC: | 43251-3340-1 |
| Package Description: | 1 TUBE in 1 CARTON (43251-3340-1) > 56 g in 1 TUBE |
NDC Information of Flexitol Medicated Foot
| NDC Code | 43251-3340-1 |
| Proprietary Name | Flexitol Medicated Foot |
| Package Description | 1 TUBE in 1 CARTON (43251-3340-1) > 56 g in 1 TUBE |
| Product NDC | 43251-3340 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tolnaftate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120811 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | LaCorium Health International Pty Ltd |
| Substance Name | TOLNAFTATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
