Arnica Plus Gel
NDC Package 70163-0203-2

11-digit billing NDC: 70163020302
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Arnica Plus (arnica montana, hamamelis virginiana, rhus tox) gel is ■ Adults and children 12 years and over: apply a thin layer to affected area at least 3 times daily or as needed. This formulation utilizes a gel delivery system. Marketed by Naturalcare, this product is identified by NDC 70163-0203.

Identification & Billing

NDC Package Code
70163-0203-2
Package Description
1 BOTTLE, PUMP in 1 CARTON / 113.4 g in 1 BOTTLE, PUMP (70163-0203-1)
Product Code
70163-0203
11-Digit Billing Format
70163020302

Clinical Specifications

Proprietary Name
Arnica Plus
Non-Proprietary Name
Arnica Montana, Hamamelis Virginiana, Rhus Tox
Substance Name
Arnica Montana Whole; Hamamelis Virginiana Root Bark/stem Bark; Toxicodendron Pubescens Leaf
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)
Usage Information
■ Adults and children 12 years and over: apply a thin layer to affected area at least 3 times daily or as needed. Gently massage into the skin until fully absorbed.■ Children under 12 years of age: consult a doctor.

Regulatory & Marketing

Labeler Name
Naturalcare
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-11-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70163-0203-2 identifies a specific commercial package of 1 bottle, pump in 1 carton / 113.4 g in 1 bottle, pump (70163-0203-1) of Arnica Plus, a human over the counter drug labeled by Naturalcare. This gel is formulated for topical use and contains arnica montana whole; hamamelis virginiana root bark/stem bark; toxicodendron pubescens leaf 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 Naturalcare on September 11, 2026. The current certification is valid through December 31, 2027.

How is this Naturalcare product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70163020302. 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 (5-4-1)
70163-0203-2
11-Digit CMS (5-4-2)
70163-0203-02

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