Kiss Fungi-gone
NDC Package 42432-101-06

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Kiss Fungi-gone is shake well before usingClean area with soap and water, dry thoroughlyApply thin layer over affected area 2 times a dayFor athlete's foot, use daily for 4 weeks or as directed by a physicianAllow solution to soak into the skin before putting socks onThis product is not effective on nails and scalp. Marketed by Kiss Products, Inc., this product is identified by NDC 42432-101 and is authorized under FDA application part333C.

Identification & Billing

NDC Package Code
42432-101-06
Package Description
1 BOTTLE, WITH APPLICATOR in 1 BOX / 30 mL in 1 BOTTLE, WITH APPLICATOR (42432-101-05)
Product Code
42432-101
11-Digit Billing Format
42432010106
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Kiss Fungi-gone Anti-fungal Treatment
Dosage Form
-
Usage Information
Shake well before usingClean area with soap and water, dry thoroughlyApply thin layer over affected area 2 times a dayFor athlete's foot, use daily for 4 weeks or as directed by a physicianAllow solution to soak into the skin before putting socks onThis product is not effective on nails and scalp

Regulatory & Marketing

Labeler Name
Kiss Products, Inc.
FDA Application #
part333C
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
10-23-2012
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (42432-101). Click a package code to view its specific billing and regulatory data.

42432-101-04
1 BOTTLE, WITH APPLICATOR in 1 BOX / 15 mL in 1 BOTTLE, WITH APPLICATOR (42432-101-03)
42432-101-51
1 BOTTLE, WITH APPLICATOR in 1 BOX / 15 mL in 1 BOTTLE, WITH APPLICATOR (42432-101-11)

* 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 42432-101-06 identifies a specific commercial package of 1 bottle, with applicator in 1 box / 30 ml in 1 bottle, with applicator (42432-101-05) of Kiss Fungi-gone Anti-fungal Treatment, labeled by Kiss Products, 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 Kiss Products, Inc. on October 23, 2012. The current certification is valid through December 31, 2017.

How is this Kiss Products, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42432010106. 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)
42432-101-06
11-Digit CMS (5-4-2)
42432-0101-06

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