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NDC 50436-9991 Medrox

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50436-9991?
  4. Medrox 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:
50436-9991
Proprietary Name:
Medrox
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unit Dose Services
Labeler Code:
50436
Product Label ID:
1844febf-30be-40ba-b0c1-5cffe6c6a7d0
Start Marketing Date: [9]
06-13-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 50436-9991?

The NDC code 50436-9991 is assigned by the FDA to the product Medrox which is product labeled by Unit Dose Services. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50436-9991-1 5 g in 1 box . 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 Medrox?

Adults and children 12 years and over apply to affected area: change patch 1 to 2 times dailyChildren under 12 years, consult physician before useHow to apply:Clean and dry affected areaCut open pouch and remove patchRemove protective film and apply directly to area of painApply to affected area not more than 3 times dailyWash hands with soap after applying patchReseal pouch containing unused patches

Which are Medrox UNII Codes?

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

Which are Medrox 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 Medrox?

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: 1300889 - capsaicin 0.0375 % / menthol 5 % Medicated Patch
  • RxCUI: 1300889 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG Medicated Patch

* 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".