Eversmile Ipr Glide Gel
NDC Package 72655-400-01

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

Package Information

Eversmile Ipr Glide (2.7% sodium fluoride gel) gel is directions For Use:IPR procedure: Dispense IPR Glide directly to theinterproximal tooth surfaces or to IPR cuttinginstruments. This formulation utilizes a gel delivery system. Marketed by Everbrands, Inc. Dba Everpure, Inc., this product is identified by NDC 72655-400.

Identification & Billing

NDC Package Code
72655-400-01
Package Description
1 SYRINGE, PLASTIC in 1 BOX / 4 mL in 1 SYRINGE, PLASTIC
Product Code
11-Digit Billing Format
72655040001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Eversmile Ipr Glide
Non-Proprietary Name
2.7% Sodium Fluoride Gel
Substance Name
Sodium Fluoride
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.
Active Ingredient(s)
Usage Information
Directions For Use:IPR procedure: Dispense IPR Glide directly to theinterproximal tooth surfaces or to IPR cuttinginstruments. Perform IPR procedure and replenishIPR Glide as needed. Rinse teeth with water. Informpatient not to swallow IPR Glide.In-Office Post IPR Renewal: Rinse teeth with water,air dry and apply IPR Glide directly to teeth surfaceswhere IPR was performed. Have patient spit outexcess IPR Glide and inform patient to keep surfacesdry for 30 minutes avoiding food and liquids. Alignersmay be worn to prevent saliva contamination.At-home Post IPR Renewal: Apply IPR Glide insideof aligners at the location where IPR was performed.Your dentist can use a marker and indicate where toapply the IPR Glide. Place aligners in mouth and wipeoff any excess IPR Glide using a tissue. Allow IPR Glideto remain on teeth for 5-10 minutes, then removealigners and spit out any excess. Keep surfaces dryfor 30 minutes avoiding food and liquids.

Regulatory & Marketing

Labeler Name
Everbrands, Inc. Dba Everpure, Inc.
Product Type
Human Prescription 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
04-10-2026
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 (72655-400). Click a package code to view its specific billing and regulatory data.

1 SYRINGE, PLASTIC in 1 BOX / 1 mL in 1 SYRINGE, PLASTIC

* 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 72655-400-01 identifies a specific commercial package of 1 syringe, plastic in 1 box / 4 ml in 1 syringe, plastic of Eversmile Ipr Glide, a human prescription drug labeled by Everbrands, Inc. Dba Everpure, Inc.. This gel is formulated for dental 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 Everbrands, Inc. Dba Everpure, Inc. on April 10, 2026. The current certification is valid through December 31, 2027.

How is this Everbrands, Inc. Dba Everpure, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72655040001. 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)
72655-400-01
11-Digit CMS (5-4-2)
72655-0400-01

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