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  4. NDC Product Code: 51452-005 Cold Spot Point Relief

NDC 51452-005 Cold Spot Point Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51452-005?
  4. Cold Spot Point 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:
51452-005
Proprietary Name:
Cold Spot Point Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fabrication Enterprises, Inc.
Labeler Code:
51452
Product Label ID:
28b9127e-d9bc-4da4-8444-07246ebe4a62
Start Marketing Date: [9]
10-13-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51452-005-04

Package Description: 4 mL in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 51452-005?

The NDC code 51452-005 is assigned by the FDA to the product Cold Spot Point Relief which is product labeled by Fabrication Enterprises, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51452-005-04 4 ml in 1 tube, with applicator . 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 Cold Spot Point Relief?

For temporary relief of minor aches and pains of the muscles and joints associated with simple backache, arthritis, bruises, strains and/or sprains.

Which are Cold Spot Point Relief UNII Codes?

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

Which are Cold Spot Point 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 Cold Spot Point 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: 1045442 - menthol 12 % / methyl salicylate 4 % Topical Gel
  • RxCUI: 1045442 - menthol 0.12 MG/MG / methyl salicylate 0.04 MG/MG Topical Gel
  • RxCUI: 1235996 - ColdSpot POINT RELIEF 12 % / 4 % Topical Gel
  • RxCUI: 1235996 - menthol 0.12 MG/MG / methyl salicylate 0.04 MG/MG Topical Gel [Cold Spot with Methyl Salicylate]
  • RxCUI: 1235996 - Cold Spot Point Relief with Methyl Salicylate (menthol 12 % / methyl salicylate 4 % ) Topical Gel

* 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".