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  4. NDC Product Code: 10096-4423 Foot Works Cracked Heel

NDC 10096-4423 Foot Works Cracked Heel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10096-4423?
  4. Foot Works Cracked Heel Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10096-4423
Proprietary Name:
Foot Works Cracked Heel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avon Products, Inc.
Labeler Code:
10096
Product Label ID:
b03b24ce-0790-4b79-ae7c-d2e734e18472
Start Marketing Date: [9]
05-30-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 10096-4423?

The NDC code 10096-4423 is assigned by the FDA to the product Foot Works Cracked Heel which is product labeled by Avon Products, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10096-4423-1 50 ml in 1 tube , 10096-4423-2 75 ml in 1 tube . 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 Works Cracked Heel?

Uses• first aid to help reduce the risk of skin infection in minor cuts, scrapes and burns• first aid for the temporary relief of pain in minor cuts, scrapes and burns

Which are Foot Works Cracked Heel UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Foot Works Cracked Heel?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1424037 - benzalkonium chloride 0.13 % / lidocaine 2 % Topical Cream
  • RxCUI: 1424037 - benzalkonium chloride 1.3 MG/ML / lidocaine 20 MG/ML Topical Cream

* Please review the disclaimer below.

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".