Chemtox Liquid
NDC Package 43857-0546-1

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

Package Information

Chemtox (triticum aestivum, berberis vulgaris, glycyrrhiza glabra, lappa major, rhamnus frangula, rhamnus purshiana, stillingia sylvatica, trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, glandula suprarenalis suis, hepar suis, lymph node (suis), thyroidinum (suis), belladonna, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum, phosphorus, salicylicum acidum, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum, potassium sorbate,) liquids is for temporary relief of weakness & exhaustion, minor abdominal cramps & bloating, and vomiting. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0546.

Identification & Billing

NDC Package Code
43857-0546-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43857-0546
11-Digit Billing Format
43857054601

Clinical Specifications

Proprietary Name
Chemtox
Non-Proprietary Name
Triticum Aestivum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Xanthoxylum Fraxineum, Phytolacca Decandra, Glandula Suprarenalis Suis, Hepar Suis, Lymph Node (suis), Thyroidinum (suis), Belladonna, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Salicylicum Acidum, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum, Potassium Sorbate,
Substance Name
Triticum Aestivum Whole; Berberis Vulgaris Root Bark; Glycyrrhiza Glabra; Arctium Lappa Root; Frangula Alnus Bark; Frangula Purshiana Bark; Stillingia Sylvatica Root; Trifolium Pratense Flower; Zanthoxylum Americanum Bark; Phytolacca Americana Root; Sus Scrofa Adrenal Gland; Pork Liver; Sus Scrofa Lymph; Thyroid; Atropa Belladonna Whole; Lycopodium Clavatum Spore; Nitric Acid; Strychnos Nux-vomica Seed; Phosphoric Acid; Phosphorus; Salicylic Acid; Cortisone Acetate; Eugenol; Stearyl Alcohol; Xylitol; Estrone; Benzoic Acid; Chlorine; Potassium Sorbate; Sorbitol; Resorcinol; Benzyl Alcohol; Lactic Acid, Dl-; Isopropyl Palmitate; Boric Acid; Acetic Acid; Phenylbutazone; Petrolatum; Lead; Corticotropin
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 weakness & exhaustion, minor abdominal cramps & bloating, and vomiting. For temporary relief of weakness & exhaustion, minor abdominal cramps & bloating, and vomiting.

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
12-26-2019
End Marketing Date
06-07-2028
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 43857-0546-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Chemtox, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains triticum aestivum whole; berberis vulgaris root bark; glycyrrhiza glabra; arctium lappa root; frangula alnus bark; frangula purshiana bark; stillingia sylvatica root; trifolium pratense flower; zanthoxylum americanum bark; phytolacca americana root; sus scrofa adrenal gland; pork liver; sus scrofa lymph; thyroid; atropa belladonna whole; lycopodium clavatum spore; nitric acid; strychnos nux-vomica seed; phosphoric acid; phosphorus; salicylic acid; cortisone acetate; eugenol; stearyl alcohol; xylitol; estrone; benzoic acid; chlorine; potassium sorbate; sorbitol; resorcinol; benzyl alcohol; lactic acid, dl-; isopropyl palmitate; boric acid; acetic acid; phenylbutazone; petrolatum; lead; corticotropin 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 December 26, 2019.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857054601. 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)
43857-0546-1
11-Digit CMS (5-4-2)
43857-0546-01

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