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  4. NDC Product Code: 50488-1701 Mencaps

NDC 50488-1701 Mencaps

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50488-1701?
  4. Mencaps 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:
50488-1701
Proprietary Name:
Mencaps
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Alexso Inc
Labeler Code:
50488
Product Label ID:
09299ae8-ab15-4291-ab51-f476c9e2f0fd
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 50488-1701?

The NDC code 50488-1701 is assigned by the FDA to the product Mencaps which is product labeled by Alexso Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50488-1701-1 3 pouch in 1 box / 5 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 Mencaps?

Adults and children 12 years and over: Apply 1 patch to the affected area of intact skin up to 3 times a day. Do not leave patch on for more than 8 hours at a time. Instructions for Use: •Clean and dry the affected area.•Open pouch and remove one patch.•Remove any protective film and apply directly to affected area of pain. Apply immediately after removal from the protective envelope.•Wash hands with soap and water after handling the patches.•Reseal pouch containing unused patches after each use. Do not store patch outside the sealed envelope.•Discontinue use at least 1 hour before a bath or shower and do not use immediately after a bath or shower.•Fold used patches so that the adhesive side sticks to itself and safely discard used patches or pieces of cut patches where children and pets cannot get to them.

Which are Mencaps UNII Codes?

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

Which are Mencaps 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 Mencaps?

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: 1658663 - capsaicin 0.0225 % / menthol 4.5 % Medicated Patch
  • RxCUI: 1658663 - capsaicin 0.000225 MG/MG / menthol 0.045 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".