Rhus Toxicodendron Mt Tincture
NDC Package 66096-752-08

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Rhus Toxicodendron Mt (rhus toxicodendron) tinctures is a human otc drug administered via oral route. This formulation utilizes a tincture delivery system. Marketed by Ohm Pharma Inc., this product is identified by NDC 66096-752.

Identification & Billing

NDC Package Code
66096-752-08
Package Description
.25 L in 1 BOTTLE
Product Code
11-Digit Billing Format
66096075208

Clinical Specifications

Proprietary Name
Rhus Toxicodendron Mt
Non-Proprietary Name
Rhus Toxicodendron
Substance Name
Toxicodendron Pubescens Leaf
Dosage Form
Tincture - An alcoholic or hydroalcoholic solution prepared from vegetable materials or from chemical substances.
Administration Route
Oral - Administration to or by way of the mouth.

Regulatory & Marketing

Labeler Name
Ohm Pharma 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
03-01-2019
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 66096-752-08 identifies a specific commercial package of .25 l in 1 bottle of Rhus Toxicodendron Mt, a human over the counter drug labeled by Ohm Pharma Inc.. This tincture is formulated for oral use and contains 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 Ohm Pharma Inc. on March 01, 2019. The current certification is valid through December 31, 2026.

How is this Ohm Pharma Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 66096075208. 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)
66096-752-08
11-Digit CMS (5-4-2)
66096-0752-08

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