Pro-Den Rx - 59883-821-02 - (Sodium Fluoride)

Alphabetical Index


Drug Information of Pro-Den Rx

Product NDC: 59883-821
Proprietary Name: Pro-Den Rx
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): 4.3    g/g & nbsp;   Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Pro-Den Rx

Product NDC: 59883-821
Labeler Name: Zila Therapeutics, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081121

Package Information of Pro-Den Rx

Package NDC: 59883-821-02
Package Description: 1 TUBE in 1 CARTON (59883-821-02) > 56 g in 1 TUBE

NDC Information of Pro-Den Rx

NDC Code 59883-821-02
Proprietary Name Pro-Den Rx
Package Description 1 TUBE in 1 CARTON (59883-821-02) > 56 g in 1 TUBE
Product NDC 59883-821
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 20081121
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Zila Therapeutics, Inc.
Substance Name SODIUM FLUORIDE
Strength Number 4.3
Strength Unit g/g
Pharmaceutical Classes

Complete Information of Pro-Den Rx


General Information