Ultra Strength Pain Relief Balm
NDC Package 76168-331-18

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.

Ultra Strength Pain Relief Balm is for adults and children over 12, rub well on the affected area. Marketed by Velocity Pharma Llc, this product is identified by NDC 76168-331 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
76168-331-18
Package Description
1 JAR in 1 PACKAGE / 18 g in 1 JAR
Product Code
76168-331
11-Digit Billing Format
76168033118
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ultra Strength Pain Relief Balm Ultra Strength
Dosage Form
-
Usage Information
For adults and children over 12, rub well on the affected area. Repeat 3 to 4 times dailyFor children 12 years of age or younger, consult a doctor before use.

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
09-10-2020
Listing Expiration
12-31-2023
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 76168-331-18 identifies a specific commercial package of 1 jar in 1 package / 18 g in 1 jar of Ultra Strength Pain Relief Balm Ultra Strength, 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 September 10, 2020. The current certification is valid through December 31, 2023.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76168033118. 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)
76168-331-18
11-Digit CMS (5-4-2)
76168-0331-18

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