Pro-Den Rx - 59883-648-04 - (Stannous Fluoride)

Alphabetical Index


Drug Information of Pro-Den Rx

Product NDC: 59883-648
Proprietary Name: Pro-Den Rx
Non Proprietary Name: Stannous Fluoride
Active Ingredient(s): 4.3    g/g & nbsp;   Stannous Fluoride
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Pro-Den Rx

Product NDC: 59883-648
Labeler Name: Zila Therapeutics, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081013

Package Information of Pro-Den Rx

Package NDC: 59883-648-04
Package Description: 1 TUBE in 1 CARTON (59883-648-04) > 122 g in 1 TUBE

NDC Information of Pro-Den Rx

NDC Code 59883-648-04
Proprietary Name Pro-Den Rx
Package Description 1 TUBE in 1 CARTON (59883-648-04) > 122 g in 1 TUBE
Product NDC 59883-648
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Stannous Fluoride
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 20081013
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Zila Therapeutics, Inc.
Substance Name STANNOUS FLUORIDE
Strength Number 4.3
Strength Unit g/g
Pharmaceutical Classes

Complete Information of Pro-Den Rx


General Information