Arnica Gel
NDC Package 0363-0139-26

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

Package Information

Arnica Gel (arnica) gel is temporarily relieves muscel pain and stiffness due to minor injuries, over exertion and fallsreduces pain, swelling and discoloration from bruisesThis product is used as. This formulation utilizes a gel delivery system. Marketed by Walgreens, this product is identified by NDC 0363-0139.

Identification & Billing

NDC Package Code
0363-0139-26
Package Description
74 g in 1 PACKAGE
Product Code
0363-0139
11-Digit Billing Format
00363013926

Clinical Specifications

Proprietary Name
Arnica Gel
Non-Proprietary Name
Arnica
Substance Name
Arnica Montana
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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)
ARNICA MONTANA 1 [hp_X]/g
Usage Information
Temporarily relieves muscel pain and stiffness due to minor injuries, over exertion and fallsreduces pain, swelling and discoloration from bruisesThis product is used as . Trauma, muscle pain, and, stiffness, swelling from injuries, discoloration from bruising

Regulatory & Marketing

Labeler Name
Walgreens
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
07-15-2021
Listing Expiration
12-31-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0363-0139-26 identifies a specific commercial package of 74 g in 1 package of Arnica Gel, a human over the counter drug labeled by Walgreens. This gel is formulated for topical use and contains arnica montana 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 Walgreens on July 15, 2021. The current certification is valid through December 31, 2026.

How is this Walgreens product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363013926. 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)
0363-0139-26
11-Digit CMS (5-4-2)
00363-0139-26

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