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Nailene Antifungal Treatment - 60193-102-02 - (TOLNAFTATE)

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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

Complete Information of Nailene Antifungal Treatment


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