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  5. NDC Package Code: 83004-016-01 Antifungal Foot Treatment

NDC Package 83004-016-01 Antifungal Foot Treatment

View Billable Units, 11-Digit Format, RxNorm

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 inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
83004-016-01
Package Description:
1 TUBE in 1 CARTON / 20 g in 1 TUBE
Product Code:
83004-016
Proprietary Name:
Antifungal Foot Treatment
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
11-Digit NDC Billing Format:
83004001601
Labeler Name:
Rida Llc
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
02-27-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
I
Code Structure:

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 disclaimer below.

Frequently Asked Questions

What is NDC 83004-016-01?

The NDC Packaged Code 83004-016-01 is assigned to a package of 1 tube in 1 carton / 20 g in 1 tube of Antifungal Foot Treatment, labeled by Rida Llc. The product's dosage form is and is administered via form.

Is NDC 83004-016 included in the NDC Directory?

No, Antifungal Foot Treatment with product code 83004-016 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rida Llc on February 27, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 83004-016-01?

The 11-digit format is 83004001601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-283004-016-015-4-283004-0016-01