59883-720 : Pro-den Rx 1.8 g/g Oral Gel


NDC: 59883-720
Labeler: Zila Therapeutics, Inc.
Product Type: Human OTC Drug
Drug Name:  Pro-den Rx
Dosage Form: Oral Gel
Application #: part355
Rev. Date: 


NDC Package Codes:

  • 59883-720-08: 1 TUBE IN 1 CARTON (59883‑720‑08) > 283.5 G IN 1 TUBE

Active Ingredients:

  • Stannous Fluoride

Dosage Strength:

  • 1.53 mg/g

Related Products:

Based on records with the same trade name.
  • 59883-166 Pro-den Rx .044 ml/Ml Oral Gel by Zila Therapeutics, Inc.
  • 59883-168 Pro-den Rx .044 ml/Ml Oral Gel by Zila Therapeutics, Inc.
  • 59883-648 Pro-den Rx 1.3 mg/ml Oral Gel by Zila Therapeutics, Inc.
  • 59883-820 Pro-den Rx 4.3 g/g Oral Gel by Zila Therapeutics, Inc.
  • 59883-821 Pro-den Rx 4.3 g/g Oral Gel by Zila Therapeutics, Inc.
  • 59883-824 Pro-den Rx 4.3 g/g Oral Gel by Zila Therapeutics, Inc.
  • 59883-826 Pro-den Rx 4.3 g/g Oral Gel by Zila Therapeutics, Inc.
  • 59883-920 Pro-den Rx .9 mg/ml Oral Rinse by Zila Therapeutics, Inc.
  • 59883-922 Pro-den Rx .9 mg/ml Oral Rinse by Zila Therapeutics, Inc.
  • 59883-911 Pro-den Rx .9 mg/ml Oral Rinse by Den-mat Holdings, LLC
  • 59883-912 Pro-den Rx .9 mg/ml Oral Rinse by Den-mat Holdings, LLC

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.