Perio Armor Gel
NDC Package 10129-032-03

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Perio Armor (1.7% hydrogen peroxide) gel is for children under 2 years of age, consult a dentist or physician before use. This formulation utilizes a gel delivery system. Marketed by Gingi-pak A Division Of The Belport, this product is identified by NDC 10129-032.

Identification & Billing

NDC Package Code
10129-032-03
Package Description
1 TUBE in 1 BOX / 88.7 mL in 1 TUBE
Product Code
11-Digit Billing Format
10129003203
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Perio Armor
Non-Proprietary Name
1.7% Hydrogen Peroxide
Substance Name
Hydrogen Peroxide
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
  • Dental - Administration to a tooth or teeth.
  • Periodontal - Administration around a tooth.
Active Ingredient(s)
Usage Information
For children under 2 years of age, consult a dentist or physician before use. For adults and children 2 years of age or older: 1. Remove cap and cut the tip of the tube at the narrow end. 2. Apply several drops of the gel directly onto the affected area in the mouth. 3. Leave the gel on the affected area for at least 60 seconds, then spit. 4. Use up to 4 times daily after meals, at bedtime, or as directed by a dentist or physician.

Regulatory & Marketing

Labeler Name
Gingi-pak A Division Of The Belport
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
10-25-2022
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 10129-032-03 identifies a specific commercial package of 1 tube in 1 box / 88.7 ml in 1 tube of Perio Armor, a human over the counter drug labeled by Gingi-pak A Division Of The Belport. This gel is formulated for dental; periodontal use and contains hydrogen peroxide 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 Gingi-pak A Division Of The Belport on October 25, 2022. The current certification is valid through December 31, 2026.

How is this Gingi-pak A Division Of The Belport product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 10129003203. 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)
10129-032-03
11-Digit CMS (5-4-2)
10129-0032-03

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