Dentek Instant Pain Relief
NDC Package 83062-410-04

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Dentek Instant Pain Relief is dip applicator into liquidAdults and children 2 years of age and older: Apply a small amount of product to the affected area. Marketed by Iimed Medical Mexicana S. De R.l. De C.v, this product is identified by NDC 83062-410 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
83062-410-04
Package Description
1 VIAL, GLASS in 1 CARTON / 3.5 mL in 1 VIAL, GLASS (83062-410-03)
Product Code
83062-410
11-Digit Billing Format
83062041004
RxNorm Crosswalk
  • RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
  • RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution

Clinical Specifications

Proprietary Name
Dentek Instant Pain Relief Maximum Strength
Dosage Form
-
Usage Information
Dip applicator into liquidAdults and children 2 years of age and older: Apply a small amount of product to the affected area. Use up to 4 times daily or as directed by a dentist or doctor.Children under 12 years of age: Should be supervised in the use of this product.Children under 2 years of age: Ask a dentist or doctor.

Regulatory & Marketing

Labeler Name
Iimed Medical Mexicana S. De R.l. De C.v
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-10-2022
Listing Expiration
12-31-2024
Exclude Flag
I
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 83062-410-04 identifies a specific commercial package of 1 vial, glass in 1 carton / 3.5 ml in 1 vial, glass (83062-410-03) of Dentek Instant Pain Relief Maximum Strength, labeled by Iimed Medical Mexicana S. De R.l. De C.v. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Iimed Medical Mexicana S. De R.l. De C.v on October 10, 2022. The current certification is valid through December 31, 2024.

How is this Iimed Medical Mexicana S. De R.l. De C.v product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83062041004. 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)
83062-410-04
11-Digit CMS (5-4-2)
83062-0410-04

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