Arthri-support
NDC Package 43078-001-30

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.

Arthri-support is • Adults and children under 12 years of age and older: apply to affected area no more than 3 to 4 times daily.• Children under 12: consult a physician.• Apply generously and massage into affected areas until completely absorbed.• Apply before and after sports or exercise to help soothe aching muscles, muscle strain, and stiffness. Marketed by Pure Science International, Inc., this product is identified by NDC 43078-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
43078-001-30
Package Description
85 g in 1 TUBE
Product Code
43078-001
11-Digit Billing Format
43078000130
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Arthri-support
Dosage Form
-
Usage Information
• Adults and children under 12 years of age and older: apply to affected area no more than 3 to 4 times daily.• Children under 12: consult a physician.• Apply generously and massage into affected areas until completely absorbed.• Apply before and after sports or exercise to help soothe aching muscles, muscle strain, and stiffness. Repeat as needed up to four times a day.

Regulatory & Marketing

Labeler Name
Pure Science International, Inc.
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
12-01-2007
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 43078-001-30 identifies a specific commercial package of 85 g in 1 tube of Arthri-support, labeled by Pure Science International, 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 Pure Science International, Inc. on December 01, 2007. The current certification is valid through December 31, 2017.

How is this Pure Science International, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43078000130. 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)
43078-001-30
11-Digit CMS (5-4-2)
43078-0001-30

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