Purewellness Fungal Fusion Antifungal And Antimicrobial Kit
NDC Package 87817-200-01

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

Package Information

Purewellness Fungal Fusion Antifungal And Antimicrobial Kit (fungal fusion antifungal and antimicrobial kit) kits is uses■ cures most athlete’s foot (tineapedis), jock itch (tinea cruris) and ringworm(tinea corporis) ■ relieves itching, cracking,burning and scaling, which accompany theseconditions Uses ■ cures most athlete’s foot (tineapedis) relieves discomfort, irritation,cracking, scaly skin between the toes, andburning feet ■ clinically proven to preventmost athlete’s foot (tinea pedis) with daily use. This formulation utilizes a kit delivery system. Marketed by Purewellness Llc, this product is identified by NDC 87817-200 and is authorized under FDA application M005.

Identification & Billing

NDC Package Code
87817-200-01
Package Description
1 KIT in 1 CARTON * 1 BOTTLE in 1 KIT (87817-110-01) / 57 g in 1 BOTTLE * 1 BOTTLE, GLASS in 1 KIT (87817-101-01) / 30 mL in 1 BOTTLE, GLASS
Product Code
87817-200
11-Digit Billing Format
87817020001

Clinical Specifications

Proprietary Name
Purewellness Fungal Fusion Antifungal And Antimicrobial Kit
Non-Proprietary Name
Fungal Fusion Antifungal And Antimicrobial Kit
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Uses■ cures most athlete’s foot (tineapedis), jock itch (tinea cruris) and ringworm(tinea corporis) ■ relieves itching, cracking,burning and scaling, which accompany theseconditions Uses ■ cures most athlete’s foot (tineapedis) relieves discomfort, irritation,cracking, scaly skin between the toes, andburning feet ■ clinically proven to preventmost athlete’s foot (tinea pedis) with daily use

Regulatory & Marketing

Labeler Name
Purewellness Llc
Product Type
Human Otc Drug
FDA Application #
M005
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-06-2026
Listing Expiration
12-31-2027
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 87817-200-01 identifies a specific commercial package of 1 kit in 1 carton * 1 bottle in 1 kit (87817-110-01) / 57 g in 1 bottle * 1 bottle, glass in 1 kit (87817-101-01) / 30 ml in 1 bottle, glass of Purewellness Fungal Fusion Antifungal And Antimicrobial Kit, a human over the counter drug labeled by Purewellness Llc. This kit is formulated for use and contains 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 Purewellness Llc on July 06, 2026. The current certification is valid through December 31, 2027.

How is this Purewellness Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87817020001. 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 (5-3-2)
87817-200-01
11-Digit CMS (5-4-2)
87817-0200-01

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