Ultra Strength Pain Relief
NDC Package 41520-317-00

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 is • shake well• adults and children 2 years of age and older: spray on affected area, not more than 3 to 4 times daily• children under 2 years of age: consult a doctor. Marketed by Car One, this product is identified by NDC 41520-317 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
41520-317-00
Package Description
118 mL in 1 CAN
Product Code
41520-317
11-Digit Billing Format
41520031700
RxNorm Crosswalk
  • RxCUI: 1600127 - camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Spray
  • RxCUI: 1600127 - camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical Spray

Clinical Specifications

Proprietary Name
Ultra Strength Pain Relief
Dosage Form
-
Usage Information
• shake well• adults and children 2 years of age and older: spray on affected area, not more than 3 to 4 times daily• children under 2 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Car One
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
08-26-2014
Listing Expiration
12-31-2019
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 41520-317-00 identifies a specific commercial package of 118 ml in 1 can of Ultra Strength Pain Relief, labeled by Car One. 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 Car One on August 26, 2014. The current certification is valid through December 31, 2019.

How is this Car One product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41520031700. 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)
41520-317-00
11-Digit CMS (5-4-2)
41520-0317-00

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