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  4. NDC Product Code: 76092-101 Smart Pro Medicated Analgesic Pain Relieving Cataplasm

NDC 76092-101 Smart Pro Medicated Analgesic Pain Relieving Cataplasm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76092-101?
  4. Smart Pro Medicated Analgesic Pain Relieving Cataplasm 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:
76092-101
Proprietary Name:
Smart Pro Medicated Analgesic Pain Relieving Cataplasm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
M J Winston International Ltd..
Labeler Code:
76092
Product Label ID:
ad334d10-9053-4c40-96a5-db7236564542
Start Marketing Date: [9]
07-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 76092-101?

The NDC code 76092-101 is assigned by the FDA to the product Smart Pro Medicated Analgesic Pain Relieving Cataplasm which is product labeled by M J Winston International Ltd... The product's dosage form is . The product is distributed in a single package with assigned NDC code 76092-101-05 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 Smart Pro Medicated Analgesic Pain Relieving Cataplasm?

Adults and children 12 years of age and olderclean and dry affected remove patch from filmapply to affected area not more than 3 to 4 times daily for 7 daysChildren under 12 years of age consult a doctor

Which are Smart Pro Medicated Analgesic Pain Relieving Cataplasm UNII Codes?

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

Which are Smart Pro Medicated Analgesic Pain Relieving Cataplasm 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 Smart Pro Medicated Analgesic Pain Relieving Cataplasm?

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: 853260 - camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated Patch
  • RxCUI: 853260 - camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 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".