Medicated Callus Removers
NDC Package 79481-0593-1

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.

Medicated Callus Removers is wash affected area and dry thoroughlyif necessary, cut medicated patch to fit calluscarefully adhere medicated patch directly over calluscover medicated patch with padafter 48 hours, remove medicated patchrepeat procedure every 48 hours as needed for up to 14 days (until callus is removed)may soak callus in warm water for 5 minutes to assist in removal. Marketed by Meijer Distribution Inc., this product is identified by NDC 79481-0593 and is authorized under FDA application M030.

Identification & Billing

NDC Package Code
79481-0593-1
Package Description
4 PATCH in 1 PACKAGE
Product Code
79481-0593
11-Digit Billing Format
79481059301

Clinical Specifications

Proprietary Name
Medicated Callus Removers
Dosage Form
-
Usage Information
Wash affected area and dry thoroughlyif necessary, cut medicated patch to fit calluscarefully adhere medicated patch directly over calluscover medicated patch with padafter 48 hours, remove medicated patchrepeat procedure every 48 hours as needed for up to 14 days (until callus is removed)may soak callus in warm water for 5 minutes to assist in removal

Regulatory & Marketing

Labeler Name
Meijer Distribution Inc.
FDA Application #
M030
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
02-22-2023
End Marketing Date
05-31-2026
Listing Expiration
05-31-2026
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 79481-0593-1 identifies a specific commercial package of 4 patch in 1 package of Medicated Callus Removers, labeled by Meijer Distribution Inc.. 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 Meijer Distribution Inc. on February 22, 2023. The current certification is valid through May 31, 2026.

How is this Meijer Distribution Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481059301. 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)
79481-0593-1
11-Digit CMS (5-4-2)
79481-0593-01

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