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  4. NDC Product Code: 10096-0284 Footworks Maximum Strength Cracked Heel

NDC 10096-0284 Footworks Maximum Strength Cracked Heel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 10096-0284?
  4. Active Ingredients UNII Codes
  5. 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:
10096-0284
Proprietary Name:
Footworks Maximum Strength Cracked Heel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
New Avon Llc
Labeler Code:
10096
Product Label ID:
9b4b1e56-c113-4955-974d-46e687789e8e
Start Marketing Date: [9]
09-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 10096-0284-1

Package Description: 75 mL in 1 TUBE

Product Details

What is NDC 10096-0284?

The NDC code 10096-0284 is assigned by the FDA to the product Footworks Maximum Strength Cracked Heel which is product labeled by New Avon Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10096-0284-1 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.

Which are Footworks Maximum Strength Cracked Heel UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Footworks Maximum Strength 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: 1356071 - benzalkonium chloride 0.13 % / lidocaine 4 % Topical Cream
  • RxCUI: 1356071 - benzalkonium chloride 1.3 MG/ML / lidocaine 40 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".