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  4. NDC Product Code: 69418-004 Elite Pain Relief

NDC 69418-004 Elite Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69418-004?
  4. Elite Pain Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
69418-004
Proprietary Name:
Elite Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meds Direct Rx, Inc.
Labeler Code:
69418
Product Label ID:
26911234-231b-4867-8fa6-3458a352a774
Start Marketing Date: [9]
05-05-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69418-004-15

Package Description: 15 g in 1 PATCH

Product Details

What is NDC 69418-004?

The NDC code 69418-004 is assigned by the FDA to the product Elite Pain Relief which is product labeled by Meds Direct Rx, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69418-004-15 15 g in 1 patch . 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 Elite Pain Relief?

•Clean and dry affected area•Remove mesh from backing and apply to affected area•Use only one mesh at a time, and maximum of 4 mesh/day• Leave mesh on affected area for up to 8 hours•Do not use mesh for longer than 5 consecutive days•Children under 12 should consult physician prior to use

Which are Elite Pain Relief UNII Codes?

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

Which are Elite Pain Relief 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:

What is the NDC to RxNorm Crosswalk for Elite Pain Relief?

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: 1540663 - allantoin 2 % / lidocaine 4 % / petrolatum 30 % Medicated Patch
  • RxCUI: 1540663 - allantoin 0.02 MG/MG / lidocaine 0.04 MG/MG / petrolatum 0.3 MG/MG Medicated Patch

* 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".