Dr. Numb
NDC Package 52512-130-30

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.

Dr. Numb is for temporary relief of local discomfort, itching, pain, soreness or burning in the perianal area assosiated with anorectal disorders. Marketed by Ei Inc., this product is identified by NDC 52512-130 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
52512-130-30
Package Description
1 TUBE in 1 PACKAGE / 30 g in 1 TUBE
Product Code
52512-130
11-Digit Billing Format
52512013030
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Dr. Numb
Dosage Form
-
Usage Information
For temporary relief of local discomfort, itching, pain, soreness or burning in the perianal area assosiated with anorectal disorders.

Regulatory & Marketing

Labeler Name
Ei Inc.
FDA Application #
part348
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-15-2012
Listing Expiration
12-31-2017
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 52512-130-30 identifies a specific commercial package of 1 tube in 1 package / 30 g in 1 tube of Dr. Numb, labeled by Ei Inc.. 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 Ei Inc. on November 15, 2012. The current certification is valid through December 31, 2017.

How is this Ei Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52512013030. 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)
52512-130-30
11-Digit CMS (5-4-2)
52512-0130-30

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