Barielle Fungus Rx Maximum Strength Anti-fungal
NDC Package 42593-002-30

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 inactivated by the FDA.

Barielle Fungus Rx Maximum Strength Anti-fungal is - To prevent athlete's foot, wash the feet and dry thoroughly. Marketed by Fisk Industries, this product is identified by NDC 42593-002 and is authorized under FDA application part333C.

Identification & Billing

NDC Package Code
42593-002-30
Package Description
1 BOTTLE in 1 PACKAGE / 30 mL in 1 BOTTLE
Product Code
42593-002
11-Digit Billing Format
42593000230
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Barielle Fungus Rx Maximum Strength Anti-fungal
Dosage Form
-
Usage Information
- To prevent athlete's foot, wash the feet and dry thoroughly. - Apply a thin layer of the product to the feet once or twice daily ( morning and/or night ). - Supervise children in the use of this product. - Pay special attention to spaces between the toes - Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Regulatory & Marketing

Labeler Name
Fisk Industries
FDA Application #
part333C
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
01-01-2012
Listing Expiration
12-31-2017
Exclude Flag
I
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 42593-002-30 identifies a specific commercial package of 1 bottle in 1 package / 30 ml in 1 bottle of Barielle Fungus Rx Maximum Strength Anti-fungal, labeled by Fisk Industries. 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 Fisk Industries on January 01, 2012. The current certification is valid through December 31, 2017.

How is this Fisk Industries product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42593000230. 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)
42593-002-30
11-Digit CMS (5-4-2)
42593-0002-30

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