Home
>
National Drug Code (NDC)
>
Nailene Antifungal Treatment
Nailene Antifungal Treatment - 60193-102-02 - (TOLNAFTATE)
Drug Information of Nailene Antifungal Treatment
| Product NDC: | 60193-102 |
| Proprietary Name: | Nailene Antifungal Treatment |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nailene Antifungal Treatment
| Product NDC: | 60193-102 |
| Labeler Name: | Pacific Word Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130424 |
Package Information of Nailene Antifungal Treatment
| Package NDC: | 60193-102-02 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (60193-102-02) > 18 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Nailene Antifungal Treatment
| NDC Code | 60193-102-02 |
| Proprietary Name | Nailene Antifungal Treatment |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (60193-102-02) > 18 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 60193-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130424 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Pacific Word Corporation |
| Substance Name | TOLNAFTATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
