Phytogel
NDC Package 64578-0127-1

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

Package Information

Phytogel (arnica montana, calendula officinalis, hypericum perforatum, bellis perennis, calcarea fluorica, ferrum phosphoricum, ledum palustre, natrum sulphuricum, rhus tox, sulphuricum acidum, symphytum officinale) gel is a human otc drug administered via topical route. This formulation utilizes a gel delivery system. Marketed by Energetix Corporation, this product is identified by NDC 64578-0127.

Identification & Billing

NDC Package Code
64578-0127-1
Package Description
57 g in 1 TUBE
Product Code
64578-0127
11-Digit Billing Format
64578012701

Clinical Specifications

Proprietary Name
Phytogel
Non-Proprietary Name
Arnica Montana, Calendula Officinalis, Hypericum Perforatum, Bellis Perennis, Calcarea Fluorica, Ferrum Phosphoricum, Ledum Palustre, Natrum Sulphuricum, Rhus Tox, Sulphuricum Acidum, Symphytum Officinale
Substance Name
Arnica Montana; Bellis Perennis; Calcium Fluoride; Calendula Officinalis Flowering Top; Comfrey Root; Ferrum Phosphoricum; Hypericum Perforatum; Ledum Palustre Twig; Sodium Sulfate; Sulfuric Acid; 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)

Regulatory & Marketing

Labeler Name
Energetix Corporation
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-15-2016
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 64578-0127-1 identifies a specific commercial package of 57 g in 1 tube of Phytogel, a human over the counter drug labeled by Energetix Corporation. This gel is formulated for topical use and contains arnica montana; bellis perennis; calcium fluoride; calendula officinalis flowering top; comfrey root; ferrum phosphoricum; hypericum perforatum; ledum palustre twig; sodium sulfate; sulfuric acid; 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 Energetix Corporation on June 15, 2016. The current certification is valid through December 31, 2026.

How is this Energetix Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 64578012701. 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)
64578-0127-1
11-Digit CMS (5-4-2)
64578-0127-01

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