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FungiFoam
FungiFoam - 49406-004-75 - (TOLNAFTATE)
Drug Information of FungiFoam
| Product NDC: | 49406-004 |
| Proprietary Name: | FungiFoam |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FungiFoam
| Product NDC: | 49406-004 |
| Labeler Name: | The Tetra Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121031 |
Package Information of FungiFoam
| Package NDC: | 49406-004-75 |
| Package Description: | 1 BOTTLE in 1 BOX (49406-004-75) > 75 mL in 1 BOTTLE |
NDC Information of FungiFoam
| NDC Code | 49406-004-75 |
| Proprietary Name | FungiFoam |
| Package Description | 1 BOTTLE in 1 BOX (49406-004-75) > 75 mL in 1 BOTTLE |
| Product NDC | 49406-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121031 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Tetra Corporation |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
