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  4. NDC Product Code: 72826-140 Neuriterx

NDC 72826-140 Neuriterx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72826-140?
  4. Neuriterx 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:
72826-140
Proprietary Name:
Neuriterx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Semprae Laboratories Inc
Labeler Code:
72826
Product Label ID:
38130cd4-d589-4319-8a1a-b4a18dc72753
Start Marketing Date: [9]
11-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 72826-140?

The NDC code 72826-140 is assigned by the FDA to the product Neuriterx which is product labeled by Semprae Laboratories Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72826-140-14 1 container in 1 carton / 56.7 g 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 Neuriterx?

Adults and children over 18 years: Apply to affected areaMassage into painful area until thoroughly absorbedRepeat as necessary, but no more than 3 to 4 times dailyChildren 18 years or younger: ask a doctor

Which are Neuriterx UNII Codes?

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

Which are Neuriterx 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 Neuriterx?

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".