Arnicare Arthritis Cream
NDC Package 0220-9077-69

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

Arnicare Arthritis (arnica montana, harpagophytum procumbens root, harpagophytum zeyheri root) cream is uses*temporarily relieves minor joint and muscle paid and stiffness due to:arthritis minor injuries overexertion falls repetitive motions. This formulation utilizes a cream delivery system. Marketed by Boiron, this product is identified by NDC 0220-9077.

Identification & Billing

NDC Package Code
0220-9077-69
Package Description
1 TUBE in 1 BOX / 14 g in 1 TUBE
Product Code
0220-9077
11-Digit Billing Format
00220907769

Clinical Specifications

Proprietary Name
Arnicare Arthritis
Non-Proprietary Name
Arnica Montana, Harpagophytum Procumbens Root, Harpagophytum Zeyheri Root
Substance Name
Arnica Montana; Harpagophytum Procumbens Root; Harpagophytum Zeyheri Root
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
Uses*temporarily relieves minor joint and muscle paid and stiffness due to:arthritis minor injuries overexertion falls repetitive motions

Regulatory & Marketing

Labeler Name
Boiron
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-17-2022
Listing Expiration
12-31-2027
Exclude Flag
N
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0220-9077). Click a package code to view its specific billing and regulatory data.

0220-9077-63
1 TUBE in 1 BOX / 70 g in 1 TUBE
0220-9077-82
1 TUBE in 1 BOX / 120 g in 1 TUBE
0220-9077-83
1 TUBE in 1 BOX / 120 g in 1 TUBE
0220-9077-93
5 g in 1 POUCH

* 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 0220-9077-69 identifies a specific commercial package of 1 tube in 1 box / 14 g in 1 tube of Arnicare Arthritis, a human over the counter drug labeled by Boiron. This cream is formulated for topical use and contains arnica montana; harpagophytum procumbens root; harpagophytum zeyheri root 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 Boiron on March 17, 2022. The current certification is valid through December 31, 2027.

How is this Boiron product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00220907769. 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 (4-4-2)
0220-9077-69
11-Digit CMS (5-4-2)
00220-9077-69

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