Homeoplex F Liquid
NDC Package 71781-0004-1

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

Package Information

Homeoplex F (echinacea (angustifolia), phytolacca decandra, lymph node (suis), conium maculatum, ferrum iodatum, hepar sulphuris calcareum, kali muriaticum, lachesis mutus, silicea) liquids is for general support of healthy cellular matrix. This formulation utilizes a liquid delivery system. Marketed by Supplement Clinic, Llc., this product is identified by NDC 71781-0004.

Identification & Billing

NDC Package Code
71781-0004-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
71781-0004
11-Digit Billing Format
71781000401

Clinical Specifications

Proprietary Name
Homeoplex F
Non-Proprietary Name
Echinacea (angustifolia), Phytolacca Decandra, Lymph Node (suis), Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum, Kali Muriaticum, Lachesis Mutus, Silicea
Substance Name
Calcium Sulfide; Conium Maculatum Flowering Top; Echinacea Angustifolia; Ferrous Iodide; Lachesis Muta Venom; Phytolacca Americana Root; Potassium Chloride; Silicon Dioxide; Sus Scrofa Lymph
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For general support of healthy cellular matrix. For general support of healthy cellular matrix.

Regulatory & Marketing

Labeler Name
Supplement Clinic, Llc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
11-01-2017
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 71781-0004-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Homeoplex F, a human over the counter drug labeled by Supplement Clinic, Llc.. This liquid is formulated for oral use and contains calcium sulfide; conium maculatum flowering top; echinacea angustifolia; ferrous iodide; lachesis muta venom; phytolacca americana root; potassium chloride; silicon dioxide; sus scrofa lymph 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 Supplement Clinic, Llc. on November 01, 2017. The current certification is valid through December 31, 2026.

How is this Supplement Clinic, Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71781000401. 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)
71781-0004-1
11-Digit CMS (5-4-2)
71781-0004-01

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