Triherbal Capsule
NDC Package 71989-718-22

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

Triherbal (arnica montana, phytolacca decandra, sanguinaria canadensis) capsules is adults and children 12 years and older: Swallow 1-2 capsules every 4 – 6 hours as needed. This formulation utilizes a capsule delivery system. Marketed by Spaus Inc., this product is identified by NDC 71989-718.

Identification & Billing

NDC Package Code
71989-718-22
Package Description
1 BOTTLE in 1 BOX / 180 CAPSULE in 1 BOTTLE
Product Code
71989-718
11-Digit Billing Format
71989071822

Clinical Specifications

Proprietary Name
Triherbal
Non-Proprietary Name
Arnica Montana, Phytolacca Decandra, Sanguinaria Canadensis
Substance Name
Arnica Montana Whole; Phytolacca Americana Root; Sanguinaria Canadensis Root
Dosage Form
Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Adults and children 12 years and older: Swallow 1-2 capsules every 4 – 6 hours as needed. Children under 12 years: Consult a doctor.

Regulatory & Marketing

Labeler Name
Spaus Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-01-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71989-718). Click a package code to view its specific billing and regulatory data.

71989-718-20
1 BOTTLE in 1 BOX / 60 CAPSULE in 1 BOTTLE
71989-718-21
1 BOTTLE in 1 BOX / 120 CAPSULE in 1 BOTTLE

* 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 71989-718-22 identifies a specific commercial package of 1 bottle in 1 box / 180 capsule in 1 bottle of Triherbal, a human over the counter drug labeled by Spaus Inc.. This capsule is formulated for oral use and contains arnica montana whole; phytolacca americana root; sanguinaria canadensis 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 Spaus Inc. on January 01, 2026. The current certification is valid through December 31, 2026.

How is this Spaus Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71989071822. 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)
71989-718-22
11-Digit CMS (5-4-2)
71989-0718-22

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