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  4. NDC Product Code: 65923-700 Pain Relief Therapy Patch

NDC 65923-700 Pain Relief Therapy Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65923-700?
  4. Pain Relief Therapy Patch 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:
65923-700
Proprietary Name:
Pain Relief Therapy Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corp
Labeler Code:
65923
Product Label ID:
99af1a89-26d5-4366-85c3-71df27479e99
Start Marketing Date: [9]
01-31-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 65923-700?

The NDC code 65923-700 is assigned by the FDA to the product Pain Relief Therapy Patch which is product labeled by United Exchange Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65923-700-05 5 patch in 1 pouch . 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 Pain Relief Therapy Patch?

Directionsadults and children 12 years of age and older:peel off protective backing and apply sticky side to affected areacarefully remove backing from patchshould be used up to 8 hours should be used no more than 3 times a daychildren under 12 years of age:consult a doctor

Which are Pain Relief Therapy Patch UNII Codes?

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

Which are Pain Relief Therapy Patch 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 Pain Relief Therapy Patch?

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:

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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".