Vantelin Odorless Pain Relieving
NDC Package 52512-105-34

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 discontinued by the firm.

Vantelin Odorless Pain Relieving is a . Marketed by Ei Llc, this product is identified by NDC 52512-105 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
52512-105-34
Package Description
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 100 mL in 1 BOTTLE, WITH APPLICATOR
Product Code
52512-105
11-Digit Billing Format
52512010534

Clinical Specifications

Proprietary Name
Vantelin Odorless Pain Relieving
Dosage Form
-

Regulatory & Marketing

Labeler Name
Ei Llc
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
05-24-2017
End Marketing Date
07-24-2017
Listing Expiration
07-24-2017
Exclude Flag
D
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 52512-105-34 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 100 ml in 1 bottle, with applicator of Vantelin Odorless Pain Relieving, labeled by Ei Llc. 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 Llc on May 24, 2017. The current certification is valid through July 24, 2017.

How is this Ei Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52512010534. 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)
52512-105-34
11-Digit CMS (5-4-2)
52512-0105-34

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