NDC 71059-010 Foot Clean Gold

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71059-010
Proprietary Name:
Foot Clean Gold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
71059
Start Marketing Date: [9]
11-01-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 71059-010?

The NDC code 71059-010 is assigned by the FDA to the product Foot Clean Gold which is product labeled by Konel. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71059-010-02 1 bottle, plastic in 1 carton / 30 g in 1 bottle, plastic (71059-010-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Foot Clean Gold?

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

Which are Foot Clean Gold UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Foot Clean Gold Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".