Hot And Cold Lidocaine With Menthol Patch
NDC Package 76168-306-05

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

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

Hot And Cold Lidocaine With Menthol Patch is adults: apply patch to affected area for a maximum of 12 hours. Marketed by Velocity Pharma Llc, this product is identified by NDC 76168-306 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
76168-306-05
Package Description
5 PATCH in 1 BOX
Product Code
11-Digit Billing Format
76168030605
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Hot And Cold Lidocaine With Menthol Patch Pain Relief
Dosage Form
-
Usage Information
Adults: apply patch to affected area for a maximum of 12 hours. Do not use more than 1 patch every 24 hours. children: consult your physician remove protective film, gently apply to affected area.

Regulatory & Marketing

Labeler Name
Velocity Pharma 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
11-22-2019
Listing Expiration
12-31-2020
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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 76168-306-05 identifies a specific commercial package of 5 patch in 1 box of Hot And Cold Lidocaine With Menthol Patch Pain Relief, labeled by Velocity Pharma 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 Velocity Pharma Llc on November 22, 2019. The current certification is valid through December 31, 2020.

How is this Velocity Pharma Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76168030605. 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)
76168-306-05
11-Digit CMS (5-4-2)
76168-0306-05

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