Bio Biological Detox Spray
NDC Package 43857-0464-1

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Bio Biological Detox (echinacea (angustifolia), lomatium dissectum, myrrha, nasturtium aquaticum, propolis, tabebuia impetiginosa, hydrastis canadensis, thymus serpyllum, glandula suprarenalis suis, lymph node (suis), spleen (suis), thyroidinum (suis), belladonna, hypericum perforatum, phosphorus, pyrogenium, anthracinum, arsenicum album, carbolicum acidum, hepar sulphuris calcareum, tarentula cubensis, variolinum, botulinum, bacillus dysentery, gaertner bacillus, mutabile bacillus, francisella tularensis, coxiella burnetii,) sprays is for the temporary relief of weakness, burning pain, fever, pustules. This formulation utilizes a spray delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0464.

Identification & Billing

NDC Package Code
43857-0464-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
43857-0464
11-Digit Billing Format
43857046401

Clinical Specifications

Proprietary Name
Bio Biological Detox
Non-Proprietary Name
Echinacea (angustifolia), Lomatium Dissectum, Myrrha, Nasturtium Aquaticum, Propolis, Tabebuia Impetiginosa, Hydrastis Canadensis, Thymus Serpyllum, Glandula Suprarenalis Suis, Lymph Node (suis), Spleen (suis), Thyroidinum (suis), Belladonna, Hypericum Perforatum, Phosphorus, Pyrogenium, Anthracinum, Arsenicum Album, Carbolicum Acidum, Hepar Sulphuris Calcareum, Tarentula Cubensis, Variolinum, Botulinum, Bacillus Dysentery, Gaertner Bacillus, Mutabile Bacillus, Francisella Tularensis, Coxiella Burnetii,
Substance Name
Arsenic Trioxide; Atropa Belladonna; Bacillus Anthracis Immunoserum Rabbit; Botulinum Toxin Type A; Calcium Sulfide; Canis Lupus Familiaris Milk; Citharacanthus Spinicrus; Coxiella Burnetii; Echinacea Angustifolia Whole; Escherichia Coli; Francisella Tularensis; Goldenseal; Human Sputum, Bordetella Pertussis Infected; Hypericum Perforatum Whole; Lomatium Dissectum Root; Myrrh; Nasturtium Officinale; Phenol; Phosphorus; Plasmodium Malariae; Propolis Wax; Rancid Beef; Salmonella Enterica Enterica Serovar Enteritidis; Shigella Dysenteriae; Sulfur; Sus Scrofa Adrenal Gland; Sus Scrofa Lymph; Sus Scrofa Spleen; Tabebuia Impetiginosa Bark; Thymus Serpyllum Whole; Thyroid; Vaccinia Virus Strain New York City Board Of Health Live Antigen; Yersinia Pestis
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For the temporary relief of weakness, burning pain, fever, pustules. For the temporary relief of weakness, burning pain, fever, pustules.

Regulatory & Marketing

Labeler Name
Bioactive Nutritional, 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
11-02-2017
End Marketing Date
07-22-2026
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 43857-0464-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Bio Biological Detox, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This spray is formulated for oral use and contains arsenic trioxide; atropa belladonna; bacillus anthracis immunoserum rabbit; botulinum toxin type a; calcium sulfide; canis lupus familiaris milk; citharacanthus spinicrus; coxiella burnetii; echinacea angustifolia whole; escherichia coli; francisella tularensis; goldenseal; human sputum, bordetella pertussis infected; hypericum perforatum whole; lomatium dissectum root; myrrh; nasturtium officinale; phenol; phosphorus; plasmodium malariae; propolis wax; rancid beef; salmonella enterica enterica serovar enteritidis; shigella dysenteriae; sulfur; sus scrofa adrenal gland; sus scrofa lymph; sus scrofa spleen; tabebuia impetiginosa bark; thymus serpyllum whole; thyroid; vaccinia virus strain new york city board of health live antigen; yersinia pestis 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 Bioactive Nutritional, Inc. on November 02, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857046401. 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)
43857-0464-1
11-Digit CMS (5-4-2)
43857-0464-01

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