Bio Immune Liquid
NDC Package 44911-0746-1

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

Package Information

Bio Immune (chelidonium majus, lobelia inflata, rumex crispus, sambucus nigra, senega officinalis, spongia tosta, taraxacum officinale, myristica sebifera, sticta pulmonaria, sulphur, ustilago maidis, polyporus officinalis, candida albicans, carduus marianus, crotalus horridus, scrophularia nodosa, agaricus muscarius, bovista, secale cornutum, anas barbariae, hepatis et cordis extractum, anthracinum, arsenicum album, baptisia tinctoria, berberis vulgaris, botulinum, bryonia (alba), camphora, cinchona officinalis,) liquids is adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0746.

Identification & Billing

NDC Package Code
44911-0746-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
44911-0746
11-Digit Billing Format
44911074601

Clinical Specifications

Proprietary Name
Bio Immune
Non-Proprietary Name
Chelidonium Majus, Lobelia Inflata, Rumex Crispus, Sambucus Nigra, Senega Officinalis, Spongia Tosta, Taraxacum Officinale, Myristica Sebifera, Sticta Pulmonaria, Sulphur, Ustilago Maidis, Polyporus Officinalis, Candida Albicans, Carduus Marianus, Crotalus Horridus, Scrophularia Nodosa, Agaricus Muscarius, Bovista, Secale Cornutum, Anas Barbariae, Hepatis Et Cordis Extractum, Anthracinum, Arsenicum Album, Baptisia Tinctoria, Berberis Vulgaris, Botulinum, Bryonia (alba), Camphora, Cinchona Officinalis,
Substance Name
Amanita Muscaria Fruiting Body; Arsenic Trioxide; Bacillus Anthracis Immunoserum Rabbit; Baptisia Tinctoria Root; Berberis Vulgaris Root Bark; Bryonia Alba Root; Cairina Moschata Heart/liver Autolysate; Camphor (natural); Candida Albicans; Chelidonium Majus Whole; Cinchona Officinalis Bark; Claviceps Purpurea Sclerotium; Clostridium Botulinum; Crotalus Horridus Horridus Venom; Gelsemium Sempervirens Root; Human Sputum, Bordetella Pertussis Infected; Influenza A Virus A/thailand/8/2022 Ivr-237 (h3n2) Antigen (formaldehyde Inactivated); Influenza A Virus A/victoria/4897/2022 Ivr-238 (h1n1) Antigen (formaldehyde Inactivated); Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole; Laricifomes Officinalis Fruiting Body; Lobaria Pulmonaria; Lobelia Inflata Whole; Lycoperdon Utriforme Fruiting Body; Milk Thistle; Polygala Senega Root; Rancid Beef; Rumex Crispus Root; Salmonella Enterica Enterica Serovar Enteritidis; Sambucus Nigra Flowering Top; Scrophularia Nodosa Whole; Shigella Dysenteriae; Spongia Officinalis Skeleton, Roasted; Streptococcus Pneumoniae; Sulfur; Taraxacum Officinale; Ustilago Maydis; Vaccinia Virus; Variola Virus; Virola Sebifera Resin
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
Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Regulatory & Marketing

Labeler Name
Energique, 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
01-08-2026
Listing Expiration
12-31-2027
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 44911-0746-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Bio Immune, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains amanita muscaria fruiting body; arsenic trioxide; bacillus anthracis immunoserum rabbit; baptisia tinctoria root; berberis vulgaris root bark; bryonia alba root; cairina moschata heart/liver autolysate; camphor (natural); candida albicans; chelidonium majus whole; cinchona officinalis bark; claviceps purpurea sclerotium; clostridium botulinum; crotalus horridus horridus venom; gelsemium sempervirens root; human sputum, bordetella pertussis infected; influenza a virus a/thailand/8/2022 ivr-237 (h3n2) antigen (formaldehyde inactivated); influenza a virus a/victoria/4897/2022 ivr-238 (h1n1) antigen (formaldehyde inactivated); influenza b virus b/austria/1359417/2021 bvr-26 whole; influenza b virus b/phuket/3073/2013 bvr-1b whole; laricifomes officinalis fruiting body; lobaria pulmonaria; lobelia inflata whole; lycoperdon utriforme fruiting body; milk thistle; polygala senega root; rancid beef; rumex crispus root; salmonella enterica enterica serovar enteritidis; sambucus nigra flowering top; scrophularia nodosa whole; shigella dysenteriae; spongia officinalis skeleton, roasted; streptococcus pneumoniae; sulfur; taraxacum officinale; ustilago maydis; vaccinia virus; variola virus; virola sebifera resin 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 Energique, Inc. on January 08, 2026. The current certification is valid through December 31, 2027.

How is this Energique, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911074601. 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)
44911-0746-1
11-Digit CMS (5-4-2)
44911-0746-01

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