ProClearz - 29784-181-02 - (Tolnaftate)

Alphabetical Index


Drug Information of ProClearz

Product NDC: 29784-181
Proprietary Name: ProClearz
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 ProClearz

Product NDC: 29784-181
Labeler Name: Profoot, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121022

Package Information of ProClearz

Package NDC: 29784-181-02
Package Description: 1 BOTTLE, WITH APPLICATOR in 1 BOX (29784-181-02) > 30 mL in 1 BOTTLE, WITH APPLICATOR (29784-181-01)

NDC Information of ProClearz

NDC Code 29784-181-02
Proprietary Name ProClearz
Package Description 1 BOTTLE, WITH APPLICATOR in 1 BOX (29784-181-02) > 30 mL in 1 BOTTLE, WITH APPLICATOR (29784-181-01)
Product NDC 29784-181
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Tolnaftate
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20121022
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Profoot, Inc.
Substance Name TOLNAFTATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of ProClearz


General Information