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Fungi Nail Toe and Foot
Fungi Nail Toe and Foot - 55505-174-50 - (Zinc Undecylenate Undecylenic acid)
Drug Information of Fungi Nail Toe and Foot
| Product NDC: | 55505-174 |
| Proprietary Name: | Fungi Nail Toe and Foot |
| Non Proprietary Name: | Zinc Undecylenate Undecylenic acid |
| Active Ingredient(s): | 5; 20 g/20g; g/20g & nbsp; Zinc Undecylenate Undecylenic acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fungi Nail Toe and Foot
| Product NDC: | 55505-174 |
| Labeler Name: | Kramer Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120301 |
Package Information of Fungi Nail Toe and Foot
| Package NDC: | 55505-174-50 |
| Package Description: | 20 g in 1 TUBE (55505-174-50) |
NDC Information of Fungi Nail Toe and Foot
| NDC Code | 55505-174-50 |
| Proprietary Name | Fungi Nail Toe and Foot |
| Package Description | 20 g in 1 TUBE (55505-174-50) |
| Product NDC | 55505-174 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Undecylenate Undecylenic acid |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kramer Laboratories |
| Substance Name | UNDECYLENIC ACID; ZINC UNDECYLENATE |
| Strength Number | 5; 20 |
| Strength Unit | g/20g; g/20g |
| Pharmaceutical Classes |
