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  4. NDC Product Code: 55264-269 Medicated Heat

NDC 55264-269 Medicated Heat

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55264-269?
  5. Medicated Heat Uses
  6. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55264-269
Proprietary Name:
Medicated Heat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corporation
Labeler Code:
55264
Product Label ID:
74758792-aa41-4e89-97c9-8a801ab2dd9a
Start Marketing Date: [9]
05-20-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 55264-269-64

Package Description: 25 POUCH in 1 CARTON / 3 PATCH in 1 POUCH

Product Details

What is NDC 55264-269?

The NDC code 55264-269 is assigned by the FDA to the product Medicated Heat which is product labeled by United Exchange Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55264-269-64 25 pouch in 1 carton / 3 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 Medicated Heat?

This product is used as PurposeTopical AnalgesicUsesTemporarily relieves minor pain associated with:arthritissimple backachestrainssprainsbruises

Which are Medicated Heat UNII Codes?

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

* 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".