Autobrush Bubblegum Gel
NDC Package 82913-005-01

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

Package Information

Autobrush Bubblegum (sodium fluoride) gel is adults and children 2 years and older: Apply a pea-sized amount of toothpaste. This formulation utilizes a gel delivery system. Marketed by Lander Enterprises, Llc, this product is identified by NDC 82913-005 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
82913-005-01
Package Description
1 TUBE in 1 BOX / 100 g in 1 TUBE
Product Code
82913-005
11-Digit Billing Format
82913000501
RxNorm Crosswalk
  • RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste

Clinical Specifications

Proprietary Name
Autobrush Bubblegum
Non-Proprietary Name
Sodium Fluoride
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM FLUORIDE .243 g/100g
Usage Information
Adults and children 2 years and older: Apply a pea-sized amount of toothpaste. When using an autobrush, split the pea-sized amount evenly across both sides of the brush head. Brush for 30 seconds using a side-to-side or figure-8 motion. With a manual or electric toothbrush, brush thoroughly for 2 minutes. Children under 6: Supervise brushing to teach good brushing habits and minimize swallowing. Children under 2: Consult a dentist or physician.

Regulatory & Marketing

Labeler Name
Lander Enterprises, Llc
Product Type
Human Otc Drug
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-01-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 82913-005-01 identifies a specific commercial package of 1 tube in 1 box / 100 g in 1 tube of Autobrush Bubblegum, a human over the counter drug labeled by Lander Enterprises, Llc. This gel is formulated for 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 Lander Enterprises, Llc on January 01, 2026. The current certification is valid through December 31, 2027.

How is this Lander Enterprises, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82913000501. 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)
82913-005-01
11-Digit CMS (5-4-2)
82913-0005-01

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