Antifungal Foot Treatment
NDC Package 83004-016-01

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Antifungal Foot Treatment is ● adults and children 12 years and over:       ● wash the affected skin with the soap and water and dry completly before applying. Marketed by Rida Llc, this product is identified by NDC 83004-016.

Identification & Billing

NDC Package Code
83004-016-01
Package Description
1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Code
83004-016
11-Digit Billing Format
83004001601

Clinical Specifications

Proprietary Name
Antifungal Foot Treatment
Dosage Form
-
Usage Information
● adults and children 12 years and over:       ● wash the affected skin with the soap and water and dry completly before applying.       ● to open the applicator, twist the base to the ON position. Squeeze tube to dispence cream.       ● for athlete's foot between the toes: apply to affected skin between and around the toes twice a day for 1 week (morning and night), or          once a day for 4 weeks, or as directed by a doctor. Wear well-fitting, ventilated shoes. Change shoes and socks at least once daily. Wipe applicator tip with a tissue and close the applicator by twisting the base to the OFF positionwash hands after each use.Childern under 12 years: ask a doctor

Regulatory & Marketing

Labeler Name
Rida Llc
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-27-2025
End Marketing Date
02-27-2025
Listing Expiration
02-27-2025
Exclude Flag
D
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 83004-016-01 identifies a specific commercial package of 1 tube in 1 carton / 20 g in 1 tube of Antifungal Foot Treatment, labeled by Rida Llc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Rida Llc on February 27, 2025. The current certification is valid through February 27, 2025.

How is this Rida Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83004001601. 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)
83004-016-01
11-Digit CMS (5-4-2)
83004-0016-01

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