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  4. NDC Product Code: 50943-001 Top Medicated

NDC 50943-001 Top Medicated

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50943-001?
  4. Top Medicated 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:
50943-001
Proprietary Name:
Top Medicated
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A&a Medical Supplies
Labeler Code:
50943
Product Label ID:
eb440866-9a10-44ac-af1d-e76c4733325e
Start Marketing Date: [9]
05-24-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 50943-001?

The NDC code 50943-001 is assigned by the FDA to the product Top Medicated which is product labeled by A&a Medical Supplies. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50943-001-01 50 ml in 1 bottle . 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 Top Medicated?

Adults and children 3 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 to 2 times daily. After applying the product, a warm pad may be placed on the affected area for 10 minutes and then massaged as shown in the illustrations.children under 3 years of age: consult your physician.refer to the above warnings; use otherwise than as directed may be dangerous.

Which are Top Medicated UNII Codes?

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

Which are Top Medicated 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 Top Medicated?

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: 1193297 - camphor 10 % / menthol 16 % / methyl salicylate 50 % Topical Oil
  • RxCUI: 1193297 - camphor 100 MG/ML / menthol 160 MG/ML / methyl salicylate 500 MG/ML Topical Oil

* 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".