Fungus Fighter Pellet
NDC Package 55714-2557-1

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

Package Information

Fungus Fighter (candida albicans, sanicula, tellurium metallicum, torula cerevisiae, antimon. crud., arsenicum alb., baryta carb., bryonia, calc. carb., carbo veg., cuprum met., dulcamara, graphites, kali carb., lachesis, lycopodium, mezereum, nitricum ac., phosphorus, phytolacca, sepia, silicea, sulphur, sulphuricum ac., zinc. met., apis mel., thuja occ.) pellets is formulated for symptoms associated with ringworm, athlete's foot and other fungal conditions of the nails, scalp and skin. This formulation utilizes a pellet delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-2557.

Identification & Billing

NDC Package Code
55714-2557-1
Package Description
28 g in 1 BOTTLE, GLASS
Product Code
55714-2557
11-Digit Billing Format
55714255701

Clinical Specifications

Proprietary Name
Fungus Fighter
Non-Proprietary Name
Candida Albicans, Sanicula, Tellurium Metallicum, Torula Cerevisiae, Antimon. Crud., Arsenicum Alb., Baryta Carb., Bryonia, Calc. Carb., Carbo Veg., Cuprum Met., Dulcamara, Graphites, Kali Carb., Lachesis, Lycopodium, Mezereum, Nitricum Ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum Ac., Zinc. Met., Apis Mel., Thuja Occ.
Substance Name
Activated Charcoal; Antimony Trisulfide; Apis Mellifera; Arsenic Trioxide; Barium Carbonate; Bryonia Alba Root; Candida Albicans; Copper; Daphne Mezereum Bark; Graphite; Lachesis Muta Venom; Lycopodium Clavatum Spore; Nitric Acid; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Phytolacca Americana Root; Potassium Carbonate; Saccharomyces Cerevisiae; Sanicula Europaea Leaf; Sepia Officinalis Juice; Silicon Dioxide; Solanum Dulcamara Top; Sulfur; Sulfuric Acid; Tellurium; Thuja Occidentalis Leafy Twig; Zinc
Dosage Form
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Formulated for symptoms associated with ringworm, athlete's foot and other fungal conditions of the nails, scalp and skin.

Regulatory & Marketing

Labeler Name
Newton Laboratories, 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
09-02-2019
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 55714-2557-1 identifies a specific commercial package of 28 g in 1 bottle, glass of Fungus Fighter, a human over the counter drug labeled by Newton Laboratories, Inc.. This pellet is formulated for oral use and contains activated charcoal; antimony trisulfide; apis mellifera; arsenic trioxide; barium carbonate; bryonia alba root; candida albicans; copper; daphne mezereum bark; graphite; lachesis muta venom; lycopodium clavatum spore; nitric acid; oyster shell calcium carbonate, crude; phosphorus; phytolacca americana root; potassium carbonate; saccharomyces cerevisiae; sanicula europaea leaf; sepia officinalis juice; silicon dioxide; solanum dulcamara top; sulfur; sulfuric acid; tellurium; thuja occidentalis leafy twig; 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 Newton Laboratories, Inc. on September 02, 2019. The current certification is valid through December 31, 2026.

How is this Newton Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55714255701. 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)
55714-2557-1
11-Digit CMS (5-4-2)
55714-2557-01

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