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  4. NDC Product Code: 49430-053 Vexa

NDC 49430-053 Vexa

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49430-053?
  4. Vexa 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:
49430-053
Proprietary Name:
Vexa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmaceutics Corporation
Labeler Code:
49430
Product Label ID:
85933294-59de-4465-a02c-4225f0c20ce8
Start Marketing Date: [9]
03-19-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 49430-053?

The NDC code 49430-053 is assigned by the FDA to the product Vexa which is product labeled by Pharmaceutics Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49430-053-15 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 Vexa?

Clean and dry affected areaRemove mesh from backing and apply to affected areaUse only one mesh at a time, and maximum of four mesh/dayLeave mesh on affected area for up to 8 hoursDo not use mesh for longer than five consecutive daysChildren under 12 should consult physician prior to use

Which are Vexa UNII Codes?

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

Which are Vexa 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 Vexa?

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: 1540663 - allantoin 2 % / lidocaine 4 % / petrolatum 30 % Medicated Patch
  • RxCUI: 1540663 - allantoin 0.02 MG/MG / lidocaine 0.04 MG/MG / petrolatum 0.3 MG/MG Medicated Patch
  • RxCUI: 1540669 - Vexa-D 2 % / 4 % / 30 % Medicated Patch
  • RxCUI: 1540669 - allantoin 0.02 MG/MG / lidocaine 0.04 MG/MG / petrolatum 0.3 MG/MG Medicated Patch [Vexa]
  • RxCUI: 1540669 - Vexa (allantoin 2 % / lidocaine 4 % / petrolatum 30 % ) 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".