Pro-sys Paste, Dentifrice
NDC Package 66975-720-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Pro-sys (sodium fluoride) pastes is adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. This formulation utilizes a paste, dentifrice delivery system. Marketed by Benco Dental, this product is identified by NDC 66975-720 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
66975-720-01
Package Description
113.4 g in 1 TUBE
Product Code
66975-720
11-Digit Billing Format
66975072001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Pro-sys
Non-Proprietary Name
Sodium Fluoride
Substance Name
Sodium Fluoride
Dosage Form
Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
Administration Route
  • Dental - Administration to a tooth or teeth.
  • Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM FLUORIDE .11 g/100g
Usage Information
Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age: use a pea-sized amount and instruct in good brushing and rinsing habits to reduce swallowing. Supervise children as necessary until capable of using without supervision. Children under 2 years of age: Consult a dentist or doctor.

Regulatory & Marketing

Labeler Name
Benco Dental
Product Type
Human Otc Drug
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-01-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (66975-720). Click a package code to view its specific billing and regulatory data.

66975-720-02
24 g in 1 TUBE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 66975-720-01 identifies a specific commercial package of 113.4 g in 1 tube of Pro-sys, a human over the counter drug labeled by Benco Dental. This paste, dentifrice is formulated for dental; oral use and contains sodium fluoride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Benco Dental on December 01, 2025. The current certification is valid through December 31, 2027.

How is this Benco Dental product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66975072001. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
66975-720-01
11-Digit CMS (5-4-2)
66975-0720-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.