Renotox Liquid
NDC Package 43857-0655-1

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

Package Information

Renotox (triticum aestivum, asparagus officinalis, berberis vulgaris, echinacea (angustifolia), kali muriaticum, petroselinum sativum, sabal serrulata, solidago virgaurea, taraxacum officinale, uva-ursi, barosma (betulina), eupatorium purpureum, kidney (suis), bryonia (alba), mercurius corrosivus, aluminum metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, cerium metallicum,) liquids is 10 drops orally, 3 times a day. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0655.

Identification & Billing

NDC Package Code
43857-0655-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
43857-0655
11-Digit Billing Format
43857065501

Clinical Specifications

Proprietary Name
Renotox
Non-Proprietary Name
Triticum Aestivum, Asparagus Officinalis, Berberis Vulgaris, Echinacea (angustifolia), Kali Muriaticum, Petroselinum Sativum, Sabal Serrulata, Solidago Virgaurea, Taraxacum Officinale, Uva-ursi, Barosma (betulina), Eupatorium Purpureum, Kidney (suis), Bryonia (alba), Mercurius Corrosivus, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum,
Substance Name
Triticum Aestivum Whole; Asparagus; Berberis Vulgaris Root Bark; Echinacea Angustifolia Whole; Potassium Chloride; Petroselinum Crispum Whole; Saw Palmetto; Solidago Virgaurea Flowering Top; Taraxacum Officinale; Arctostaphylos Uva-ursi Leaf; Agathosma Betulina Leaf; Eutrochium Purpureum Root; Pork Kidney; Bryonia Alba Root; Mercuric Chloride; Aluminum; Antimony Trisulfide; Silver; Arsenic Trioxide; Gold; Barium Carbonate; Beryllium; Bismuth; Boron; Bromine; Cadmium; Cerium; Cesium Chloride; Chromium; Cobalt; Copper; Dysprosium; Erbium; Europium; Iron; Gadolinium; Germanium Sesquioxide; Holmium; Indium; Lithium Carbonate; Magnesium; Manganese; Mercurius Solubilis; Molybdenum; Neodymium Oxide; Nickel; Osmium; Palladium; Platinum; Lead; Praseodymium; Rhodium; Rubidium Nitrite; Samarium; Selenium; Tin; Strontium Carbonate; Terbium; Thallium; Uranyl Nitrate Hexahydrate; Vanadium; Ytterbium Oxide; Zinc; Influenza A Virus Whole; Influenza A Virus A/darwin/6/2021 (h3n2) Whole; Influenza B Virus B/austria/1359417/2021 Bvr-26 Whole; Influenza B Virus B/phuket/3073/2013 Bvr-1b Whole; Measles Virus; Botulinum Toxin Type A; Escherichia Coli; Proteus Vulgaris; Pseudomonas Aeruginosa; Proteus Morganii; Salmonella Enterica Enterica Serovar Typhi; Lanthanum; Clostridium Perfringens; Human Herpesvirus 4; Niobium; Poliovirus; Tantalum
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
10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

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
03-20-2025
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 43857-0655-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Renotox, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains triticum aestivum whole; asparagus; berberis vulgaris root bark; echinacea angustifolia whole; potassium chloride; petroselinum crispum whole; saw palmetto; solidago virgaurea flowering top; taraxacum officinale; arctostaphylos uva-ursi leaf; agathosma betulina leaf; eutrochium purpureum root; pork kidney; bryonia alba root; mercuric chloride; aluminum; antimony trisulfide; silver; arsenic trioxide; gold; barium carbonate; beryllium; bismuth; boron; bromine; cadmium; cerium; cesium chloride; chromium; cobalt; copper; dysprosium; erbium; europium; iron; gadolinium; germanium sesquioxide; holmium; indium; lithium carbonate; magnesium; manganese; mercurius solubilis; molybdenum; neodymium oxide; nickel; osmium; palladium; platinum; lead; praseodymium; rhodium; rubidium nitrite; samarium; selenium; tin; strontium carbonate; terbium; thallium; uranyl nitrate hexahydrate; vanadium; ytterbium oxide; zinc; influenza a virus whole; influenza a virus a/darwin/6/2021 (h3n2) whole; influenza b virus b/austria/1359417/2021 bvr-26 whole; influenza b virus b/phuket/3073/2013 bvr-1b whole; measles virus; botulinum toxin type a; escherichia coli; proteus vulgaris; pseudomonas aeruginosa; proteus morganii; salmonella enterica enterica serovar typhi; lanthanum; clostridium perfringens; human herpesvirus 4; niobium; poliovirus; tantalum 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 March 20, 2025. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857065501. 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)
43857-0655-1
11-Digit CMS (5-4-2)
43857-0655-01

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