Tri-relief Antifungal Solution/ Drops
NDC Package 51393-7621-4

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

Package Information

Tri-relief Antifungal (sodium chloride, silicon dioxide, and thuja occidentalis leafy twig) solution/ dropses is shake well before use. This formulation utilizes a solution/ drops delivery system. Marketed by Forces Of Nature, this product is identified by NDC 51393-7621.

Identification & Billing

NDC Package Code
51393-7621-4
Package Description
1 BOTTLE, DISPENSING in 1 CARTON / 4 mL in 1 BOTTLE, DISPENSING
Product Code
51393-7621
11-Digit Billing Format
51393762104

Clinical Specifications

Proprietary Name
Tri-relief Antifungal
Non-Proprietary Name
Sodium Chloride, Silicon Dioxide, And Thuja Occidentalis Leafy Twig
Substance Name
Silicon Dioxide; Sodium Chloride; Thuja Occidentalis Leafy Twig
Dosage Form
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Shake well before use. Wash and dry the area. Apply thin layer over the affected area 3 times daily. For athlete's foot and ringworm apply daily for 4 weeks. For jock itch, use daily for 2 weeks. If condition persists, consult a doctor. This product does not prevent the transmission of fungal infection.

Regulatory & Marketing

Labeler Name
Forces Of Nature
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
11-01-2025
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 51393-7621-4 identifies a specific commercial package of 1 bottle, dispensing in 1 carton / 4 ml in 1 bottle, dispensing of Tri-relief Antifungal, a human over the counter drug labeled by Forces Of Nature. This solution/ drops is formulated for topical use and contains silicon dioxide; sodium chloride; thuja occidentalis leafy twig 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 Forces Of Nature on November 01, 2025. The current certification is valid through December 31, 2026.

How is this Forces Of Nature product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51393762104. 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)
51393-7621-4
11-Digit CMS (5-4-2)
51393-7621-04

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