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  4. NDC Product Code: 59779-551 Cvs Medicated Pain Relieving

NDC 59779-551 Cvs Medicated Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59779-551?
  4. Cvs Medicated Pain Relieving 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:
59779-551
Proprietary Name:
Cvs Medicated Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy, Inc.
Labeler Code:
59779
Product Label ID:
84ce8bbd-51b7-4915-8e70-1d22999e34dc
Start Marketing Date: [9]
06-30-2013
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 59779-551?

The NDC code 59779-551 is assigned by the FDA to the product Cvs Medicated Pain Relieving which is product labeled by Cvs Pharmacy, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-551-40 2 pouch in 1 box / 20 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 Cvs Medicated Pain Relieving?

Directions Adults and children 12 years of age and over:Clean and dry affected areaRemove patch from filmApply to affected area not more than 3 to 4 times daily for 7 daysRemove patch from skin after at most 8 hours applicationChildren under 12 years of age: consult a doctor

Which are Cvs Medicated Pain Relieving UNII Codes?

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

Which are Cvs Medicated Pain Relieving 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 Cvs Medicated Pain Relieving?

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".