Pro-Den Rx - 59883-920-16 - (Pro-Den Rx)

Alphabetical Index


Drug Information of Pro-Den Rx

Product NDC: 59883-920
Proprietary Name: Pro-Den Rx
Non Proprietary Name: Pro-Den Rx
Active Ingredient(s): .946    mL/mL & nbsp;   Pro-Den Rx
Administration Route(s): ORAL
Dosage Form(s): RINSE
Coding System: National Drug Codes(NDC)

Labeler Information of Pro-Den Rx

Product NDC: 59883-920
Labeler Name: Zila Therapeutics, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part355
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20081001

Package Information of Pro-Den Rx

Package NDC: 59883-920-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC (59883-920-16)

NDC Information of Pro-Den Rx

NDC Code 59883-920-16
Proprietary Name Pro-Den Rx
Package Description 473 mL in 1 BOTTLE, PLASTIC (59883-920-16)
Product NDC 59883-920
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pro-Den Rx
Dosage Form Name RINSE
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Zila Therapeutics, Inc.
Substance Name SODIUM FLUORIDE
Strength Number .946
Strength Unit mL/mL
Pharmaceutical Classes

Complete Information of Pro-Den Rx


General Information