Artrex Cream
NDC Package 68354-131-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Artrex (camphor, menthol, and turpentine) cream is temporarily relieves aches and pains of muscles and joints due to arthritis, simple backache, sprains, strains, and sports injuries. This formulation utilizes a cream delivery system. Marketed by Bioved Pharmaceuticals, this product is identified by NDC 68354-131 and is authorized under FDA application M014.

Identification & Billing

NDC Package Code
68354-131-10
Package Description
10 g in 1 TUBE
Product Code
68354-131
11-Digit Billing Format
68354013110
RxNorm Crosswalk
  • RxCUI: 1551280 - camphor 5 % / menthol 3 % / turpentine oil 10 % Topical Cream
  • RxCUI: 1551280 - camphor 50 MG/ML / menthol 30 MG/ML / turpentine 100 MG/ML Topical Cream
  • RxCUI: 1551280 - camphor 5 % / menthol 3 % / turpentine 10 % Topical Cream

Clinical Specifications

Proprietary Name
Artrex
Non-Proprietary Name
Camphor, Menthol, And Turpentine
Substance Name
Camphor (natural); Menthol; Turpentine
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
Temporarily relieves aches and pains of muscles and joints due to arthritis, simple backache, sprains, strains, and sports injuries

Regulatory & Marketing

Labeler Name
Bioved Pharmaceuticals
Product Type
Human Otc Drug
FDA Application #
M014
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2004
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
Yes

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (68354-131). Click a package code to view its specific billing and regulatory data.

68354-131-60
60 g in 1 TUBE

* 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 68354-131-10 identifies a specific commercial package of 10 g in 1 tube of Artrex, a human over the counter drug labeled by Bioved Pharmaceuticals. This cream is formulated for topical use and contains camphor (natural); menthol; turpentine as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bioved Pharmaceuticals on April 01, 2004. The current certification is valid through December 31, 2026.

How is this Bioved Pharmaceuticals product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68354013110. 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)
68354-131-10
11-Digit CMS (5-4-2)
68354-0131-10

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