Dc Blister Booster Adult Kit
NDC Package 84035-014-20

11-digit billing NDC: 84035001420
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Dc Blister Booster Adult (sodium fluoride 0.24%) kits 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.Children 2 to 6 years of age: instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). This formulation utilizes a kit delivery system. Marketed by Rabbit Ind�stria E Com�rcio De Produtos De Higiene Pessoal Ltda, this product is identified by NDC 84035-014 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
84035-014-20
Package Description
1 KIT in 1 BLISTER PACK * 1 TUBE in 1 CARTON (84035-006-20) / 20 g in 1 TUBE
Product Code
84035-014
11-Digit Billing Format
84035001420

Clinical Specifications

Proprietary Name
Dc Blister Booster Adult
Non-Proprietary Name
Sodium Fluoride 0.24%
Dosage Form
Kit - A packaged collection of related material.
Administration Route
Dental - Administration to a tooth or teeth.
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 2 to 6 years of age: instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children under 6 years as necessary and use a pea-sized amount until your child is capable of using without supervision.Children under 2 years of age: do not use unless directed by a dentist or doctor or as directed by a dentist or doctor.

Regulatory & Marketing

Labeler Name
Rabbit Ind�stria E Com�rcio De Produtos De Higiene Pessoal Ltda
Product Type
Human Otc Drug
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2026
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 84035-014-20 identifies a specific commercial package of 1 kit in 1 blister pack * 1 tube in 1 carton (84035-006-20) / 20 g in 1 tube of Dc Blister Booster Adult, a human over the counter drug labeled by Rabbit Ind�stria E Com�rcio De Produtos De Higiene Pessoal Ltda. This kit is formulated for dental use and contains 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 Rabbit Ind�stria E Com�rcio De Produtos De Higiene Pessoal Ltda on September 01, 2026. The current certification is valid through December 31, 2027.

How is this Rabbit Ind�stria E Com�rcio De Produtos De Higiene Pessoal Ltda product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84035001420. 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)
84035-014-20
11-Digit CMS (5-4-2)
84035-0014-20

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