Flu-tone Liquid
NDC Package 64578-0136-1

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

Package Information

Flu-tone (anas barbariae, hepatis et cordis extractum, azadirachta indica, baptisia tinctoria, bryonia (alba), crotalus horridus, echinacea (angustifolia), eupatorium perfoliatum, ferrum phosphoricum, gelsemium sempervirens, ginkgo biloba, influenzinum, mucosa nasalis suis, phytolacca decandra, pinus sylvestris, pyrogenium, selenium metallicum, stillingia sylvatica) liquids is a human otc drug administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Energetix Corporation, this product is identified by NDC 64578-0136.

Identification & Billing

NDC Package Code
64578-0136-1
Package Description
59 mL in 1 PACKAGE
Product Code
64578-0136
11-Digit Billing Format
64578013601

Clinical Specifications

Proprietary Name
Flu-tone
Non-Proprietary Name
Anas Barbariae, Hepatis Et Cordis Extractum, Azadirachta Indica, Baptisia Tinctoria, Bryonia (alba), Crotalus Horridus, Echinacea (angustifolia), Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Ginkgo Biloba, Influenzinum, Mucosa Nasalis Suis, Phytolacca Decandra, Pinus Sylvestris, Pyrogenium, Selenium Metallicum, Stillingia Sylvatica
Substance Name
Azadirachta Indica Bark; Baptisia Tinctoria Root; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Crotalus Horridus Horridus Venom; Echinacea Angustifolia; Eupatorium Perfoliatum Flowering Top; Ferrum Phosphoricum; Gelsemium Sempervirens Root; Ginkgo; Influenza A Virus A/singapore/gp1908/2015 Ivr-180 (h1n1) Antigen (formaldehyde Inactivated); Influenza A Virus A/singapore/infimh-16-0019/2016 Nib-104 (h3n2) Antigen (formaldehyde Inactivated); Influenza B Virus B/maryland/15/2016 Antigen (formaldehyde Inactivated); Influenza B Virus B/phuket/3073/2013 Antigen (formaldehyde Inactivated); Phytolacca Americana Root; Pinus Sylvestris Leafy Twig; Rancid Beef; Selenium; Stillingia Sylvatica Root; Sus Scrofa Nasal Mucosa
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)

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
11-01-2018
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 64578-0136-1 identifies a specific commercial package of 59 ml in 1 package of Flu-tone, a human over the counter drug labeled by Energetix Corporation. This liquid is formulated for oral use and contains azadirachta indica bark; baptisia tinctoria root; bryonia alba root; cairina moschata heart/liver autolysate; crotalus horridus horridus venom; echinacea angustifolia; eupatorium perfoliatum flowering top; ferrum phosphoricum; gelsemium sempervirens root; ginkgo; influenza a virus a/singapore/gp1908/2015 ivr-180 (h1n1) antigen (formaldehyde inactivated); influenza a virus a/singapore/infimh-16-0019/2016 nib-104 (h3n2) antigen (formaldehyde inactivated); influenza b virus b/maryland/15/2016 antigen (formaldehyde inactivated); influenza b virus b/phuket/3073/2013 antigen (formaldehyde inactivated); phytolacca americana root; pinus sylvestris leafy twig; rancid beef; selenium; stillingia sylvatica root; sus scrofa nasal mucosa 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 November 01, 2018. 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: 64578013601. 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)
64578-0136-1
11-Digit CMS (5-4-2)
64578-0136-01

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