Metox Liquid
NDC Package 43742-2221-1

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

Package Information

Metox (allium sativum, arsenicum album, ascorbicum acidum, berberis vulgaris, boron, carbolicum acidum, cysteinum, formalinum, glycyrrhiza glabra, lanthanum metallicum, lappa major, l-methionine, lycopodium clavatum, mercurius solubilis, natrum muriaticum, niobium metallicum, nux vomica, phytolacca decandra, plumbum metallicum, stillingia sylvatica, tantalum metallicum, thyroidinum (suis), trifolium pratense, aluminium metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum,) liquids is 1-10 drops under the tongue, 3 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2221.

Identification & Billing

NDC Package Code
43742-2221-1
Package Description
60 mL in 1 BOTTLE, DROPPER
Product Code
43742-2221
11-Digit Billing Format
43742222101

Clinical Specifications

Proprietary Name
Metox
Non-Proprietary Name
Allium Sativum, Arsenicum Album, Ascorbicum Acidum, Berberis Vulgaris, Boron, Carbolicum Acidum, Cysteinum, Formalinum, Glycyrrhiza Glabra, Lanthanum Metallicum, Lappa Major, L-methionine, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Niobium Metallicum, Nux Vomica, Phytolacca Decandra, Plumbum Metallicum, Stillingia Sylvatica, Tantalum Metallicum, Thyroidinum (suis), Trifolium Pratense, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum,
Substance Name
Garlic; Arsenic Trioxide; Ascorbic Acid; Berberis Vulgaris Root Bark; Boron; Phenol; Cysteine; Formaldehyde Solution; Glycyrrhiza Glabra; Lanthanum; Arctium Lappa Root; Methionine; Lycopodium Clavatum Spore; Mercurius Solubilis; Sodium Chloride; Niobium; Strychnos Nux-vomica Seed; Phytolacca Americana Root; Lead; Stillingia Sylvatica Root; Tantalum; Thyroid; Trifolium Pratense Flower; Uranyl Nitrate Hexahydrate; Aluminum; Antimony Trisulfide; Silver; Gold; Barium Carbonate; Beryllium; Bismuth; Bromine; Cadmium; Cerium; Cesium Chloride; Dysprosium; Erbium; Europium; Gadolinium; Germanium Sesquioxide; Holmium; Indium; Manganese; Neodymium Oxide; Nickel; Osmium; Palladium; Platinum; Praseodymium; Rhodium; Rubidium; Samarium; Tin; Terbium; Thallium; Ytterbium Oxide; Tribasic Calcium Phosphate; Chromium; Cobalt; Copper; Iron; Iodine; Iridium; Potassium Carbonate; Lithium Carbonate; Magnesium; Molybdenum; Phosphorus; Selenium; Strontium Carbonate; Sulfur; Vanadium; Zinc
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
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Regulatory & Marketing

Labeler Name
Deseret Biologicals, 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
01-17-2025
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 43742-2221-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of Metox, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains garlic; arsenic trioxide; ascorbic acid; berberis vulgaris root bark; boron; phenol; cysteine; formaldehyde solution; glycyrrhiza glabra; lanthanum; arctium lappa root; methionine; lycopodium clavatum spore; mercurius solubilis; sodium chloride; niobium; strychnos nux-vomica seed; phytolacca americana root; lead; stillingia sylvatica root; tantalum; thyroid; trifolium pratense flower; uranyl nitrate hexahydrate; aluminum; antimony trisulfide; silver; gold; barium carbonate; beryllium; bismuth; bromine; cadmium; cerium; cesium chloride; dysprosium; erbium; europium; gadolinium; germanium sesquioxide; holmium; indium; manganese; neodymium oxide; nickel; osmium; palladium; platinum; praseodymium; rhodium; rubidium; samarium; tin; terbium; thallium; ytterbium oxide; tribasic calcium phosphate; chromium; cobalt; copper; iron; iodine; iridium; potassium carbonate; lithium carbonate; magnesium; molybdenum; phosphorus; selenium; strontium carbonate; sulfur; vanadium; zinc 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 Deseret Biologicals, Inc. on January 17, 2025. The current certification is valid through December 31, 2026.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742222101. 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)
43742-2221-1
11-Digit CMS (5-4-2)
43742-2221-01

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