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  4. NDC Product Code: 50488-6541 Lidocaine 4 Percent And Menthol 1 Percent Roll-on

NDC 50488-6541 Lidocaine 4 Percent And Menthol 1 Percent Roll-on

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50488-6541?
  4. Lidocaine 4 Percent And Menthol 1 Percent Roll-on 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:
50488-6541
Proprietary Name:
Lidocaine 4 Percent And Menthol 1 Percent Roll-on
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Alexso, Inc
Labeler Code:
50488
Product Label ID:
511ee92e-f69c-4d21-aadd-84a06aca00c2
Start Marketing Date: [9]
02-17-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50488-6541-1

Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 50488-6541?

The NDC code 50488-6541 is assigned by the FDA to the product Lidocaine 4 Percent And Menthol 1 Percent Roll-on 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 50488-6541-1 50 ml in 1 bottle, with applicator . 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 Lidocaine 4 Percent And Menthol 1 Percent Roll-on?

 adults and children 2 years and older apply externally to the affected area up to 3 to 4  times a day children under 2 years do not use except under the advice and supervision of a physician

Which are Lidocaine 4 Percent And Menthol 1 Percent Roll-on UNII Codes?

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

Which are Lidocaine 4 Percent And Menthol 1 Percent Roll-on 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 Lidocaine 4 Percent And Menthol 1 Percent Roll-on?

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: 252967 - lidocaine 4 % / menthol 1 % Topical Solution
  • RxCUI: 252967 - lidocaine 40 MG/ML / menthol 10 MG/ML Topical Solution

* 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".