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  4. NDC Product Code: 46144-162 Allevess

NDC 46144-162 Allevess

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 46144-162?
  4. Allevess 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:
46144-162
Proprietary Name:
Allevess
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Api Solutions, Inc.
Labeler Code:
46144
Product Label ID:
1982db88-d00d-4ba7-ae87-190799556709
Start Marketing Date: [9]
12-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 46144-162-01

Package Description: 3 POUCH in 1 BOX / 5 PATCH in 1 POUCH / 100 g in 1 PATCH

Product Details

What is NDC 46144-162?

The NDC code 46144-162 is assigned by the FDA to the product Allevess which is product labeled by Api Solutions, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 46144-162-01 3 pouch in 1 box / 5 patch in 1 pouch / 100 g in 1 patch. 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 Allevess?

ADULTS AND CHILDREN 16 YEARS AND OVER: APPLY DIRECTLY TO AFFECTED AREA OF PAIN; CHANGE PATCH 1 TO 2 TIMES DAILY, OR AS DIRECTED BY A DOCTOR ∙ CHILDREN UNDER 16 YEARS: ASK A DOCTOR BEFORE USINGHOW TO APPLY:− CLEAN AND DRY AFFECTED AREA - TEAR OPEN POUCH AND REMOVE ONE PATCH− REMOVE PROTECTIVE FILM AND APPLY DIRECTLY TO AFFECTED AREA OF PAIN− RESEAL POUCH CONTAINING UNUSED PATCHES AFTER EACH USE− WASH HANDS WITH SOAP AND WATER AFTER APPLYING

Which are Allevess UNII Codes?

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

Which are Allevess 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 Allevess?

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: 1552450 - capsaicin 0.05 % / menthol 5 % Medicated Patch
  • RxCUI: 1552450 - capsaicin 0.0005 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".