Biotox Bac Liquid
NDC Package 50181-0078-1

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

Package Information

Biotox Bac (mycoplasma pneumoniae, proteus (vulgaris), candida albicans, colibacillinum cum natrum muriaticum, mycobacterium paratuberculosis, pasteurellosis (pasteurella multocida), pneumococcinum, thuja occidentalis, mycobacterium avium paratuberculosis, phytolacca decandra, legionella pneumophila, shigella sonnei) liquids is for temporary relief of fever and chills. This formulation utilizes a liquid delivery system. Marketed by The Wellness Center For Research And Education, Inc., this product is identified by NDC 50181-0078.

Identification & Billing

NDC Package Code
50181-0078-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
50181-0078
11-Digit Billing Format
50181007801

Clinical Specifications

Proprietary Name
Biotox Bac 3
Non-Proprietary Name
Mycoplasma Pneumoniae, Proteus (vulgaris), Candida Albicans, Colibacillinum Cum Natrum Muriaticum, Mycobacterium Paratuberculosis, Pasteurellosis (pasteurella Multocida), Pneumococcinum, Thuja Occidentalis, Mycobacterium Avium Paratuberculosis, Phytolacca Decandra, Legionella Pneumophila, Shigella Sonnei
Substance Name
Mycoplasma Pneumoniae; Proteus Inconstans; Candida Albicans; Escherichia Coli; Mycobacterium Avium Subsp. Paratuberculosis; Pasteurella Multocida; Streptococcus Pneumoniae; Thuja Occidentalis Leafy Twig; Phytolacca Americana Root; Legionella Pneumophila; Shigella Sonnei
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 temporary relief of fever and chills. Promotes a productive wet cough and the coughing up of phlegm. expectorant. Helps relieve the presence of mucus in the stool and loose stools.  For temporary relief of fever and chills. Promotes a productive wet cough and the coughing up of phlegm. expectorant. Helps relieve the presence of mucus in the stool and loose stools.

Regulatory & Marketing

Labeler Name
The Wellness Center For Research And Education, 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
11-08-2021
End Marketing Date
12-09-2026
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 50181-0078-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Biotox Bac 3, a human over the counter drug labeled by The Wellness Center For Research And Education, Inc.. This liquid is formulated for oral use and contains mycoplasma pneumoniae; proteus inconstans; candida albicans; escherichia coli; mycobacterium avium subsp. paratuberculosis; pasteurella multocida; streptococcus pneumoniae; thuja occidentalis leafy twig; phytolacca americana root; legionella pneumophila; shigella sonnei 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 The Wellness Center For Research And Education, Inc. on November 08, 2021.

How is this The Wellness Center For Research And Education, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50181007801. 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)
50181-0078-1
11-Digit CMS (5-4-2)
50181-0078-01

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