Foot Clean Gold
NDC Package 71059-010-02

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.

Foot Clean Gold is directions: - 1 liter of water should be boiled to 100 °C - Pour the boiled water into a bucket with 1 bottle of this product - Place your feet in the bucket after the temperature of the water and solution have decreased to 38~40°C (be careful of scalding) - After leaving your feet in the bucket with the solution for 1 hour or longer, wipe the water off your feet without rinsing your feet with water - Do not use soap or cleanser for 24 hours after using this product - On average, the outer skin will start to peel in 3~10 days and will show improvements in 2~4 weeks (varies per body type) - If the amount of water used is more than the suggested amount, it may lower the efficacy. Marketed by Konel, this product is identified by NDC 71059-010.

Identification & Billing

NDC Package Code
71059-010-02
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 30 g in 1 BOTTLE, PLASTIC (71059-010-01)
Product Code
71059-010
11-Digit Billing Format
71059001002

Clinical Specifications

Proprietary Name
Foot Clean Gold
Dosage Form
-
Usage Information
Directions: - 1 liter of water should be boiled to 100 °C - Pour the boiled water into a bucket with 1 bottle of this product - Place your feet in the bucket after the temperature of the water and solution have decreased to 38~40°C (be careful of scalding) - After leaving your feet in the bucket with the solution for 1 hour or longer, wipe the water off your feet without rinsing your feet with water - Do not use soap or cleanser for 24 hours after using this product - On average, the outer skin will start to peel in 3~10 days and will show improvements in 2~4 weeks (varies per body type) - If the amount of water used is more than the suggested amount, it may lower the efficacy

Regulatory & Marketing

Labeler Name
Konel
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
11-01-2016
Listing Expiration
12-31-2023
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 71059-010-02 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 30 g in 1 bottle, plastic (71059-010-01) of Foot Clean Gold, labeled by Konel. 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 Konel on November 01, 2016. The current certification is valid through December 31, 2023.

How is this Konel product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71059001002. 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)
71059-010-02
11-Digit CMS (5-4-2)
71059-0010-02

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