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  4. NDC Product Code: 70859-028 Nudroxicin Pain Relief Roll-on

NDC 70859-028 Nudroxicin Pain Relief Roll-on

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70859-028?
  4. Nudroxicin Pain Relief Roll-on 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:
70859-028
Proprietary Name:
Nudroxicin Pain Relief Roll-on
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nucare Pharmaceuticals Inc
Labeler Code:
70859
Product Label ID:
64bc6acc-58bf-0881-e053-2a91aa0a35e4
Start Marketing Date: [9]
11-18-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 70859-028?

The NDC code 70859-028 is assigned by the FDA to the product Nudroxicin Pain Relief Roll-on which is product labeled by Nucare Pharmaceuticals Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70859-028-03 1 container in 1 carton / 90 ml in 1 container. 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 Nudroxicin Pain Relief Roll-on?

For the management of the signs and symptoms of OA [ see Clinical Studies (14.1)]

Which are Nudroxicin Pain Relief Roll-on UNII Codes?

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

Which are Nudroxicin Pain Relief Roll-on 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 Nudroxicin Pain Relief Roll-on?

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: 1989491 - capsaicin 0.025 % / menthol 6 % / methyl salicylate 25 % Topical Solution
  • RxCUI: 1989491 - capsaicin 0.25 MG/ML / menthol 60 MG/ML / methyl salicylate 250 MG/ML Topical Solution
  • RxCUI: 205323 - celecoxib 200 MG Oral Capsule

* 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".