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  4. NDC Product Code: 41167-7516 Capzasin Quick Relief

NDC 41167-7516 Capzasin Quick Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41167-7516?
  4. Capzasin Quick Relief 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 expired due to lack of listing certification.

Get all the details for National Drug Code (NDC) 41167-7516 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
41167-7516
Proprietary Name:
Capzasin Quick Relief
Product Type: [3]
Labeler Name: [5]
Chattem, Inc.
Labeler Code:
41167
Product Label ID:
d6c313a3-8dc6-4231-95b6-ac9399e1c1be
FDA Application Number: [6]
M017
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
12-01-2008
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
U
Code Navigator:

Code Structure Chart

Product Details

What is NDC 41167-7516?

The NDC code 41167-7516 is assigned by the FDA to the product Capzasin Quick Relief which is product labeled by Chattem, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41167-7516-0 1 tube, with applicator in 1 carton / 42.5 g in 1 tube, 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 Capzasin Quick Relief?

Adults and children over 18 years:squeeze desired amount of Capzasin Quick Relief Gel onto affected areausing the sponge-top applicator, massage dispensed gel into painful area until thoroughly absorbedrepeat as necessary, but no more than 3 to 4 times dailyIF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATERchildren 18 years or younger: ask a doctor

Which are Capzasin Quick Relief UNII Codes?

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

Which are Capzasin Quick Relief 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 Capzasin Quick Relief?

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: 1043539 - CAPZASIN Quick Relief 0.025 % / 10 % Topical Gel
  • RxCUI: 1043539 - capsaicin 0.00025 MG/MG / menthol 0.1 MG/MG Topical Gel [Capzasin Quick Relief]
  • RxCUI: 1043539 - Capzasin Quick Relief (capsaicin 0.025 % / menthol 10 % ) Topical Gel
  • RxCUI: 855923 - capsaicin 0.025 % / menthol 10 % Topical Gel
  • RxCUI: 855923 - capsaicin 0.00025 MG/MG / menthol 0.1 MG/MG Topical Gel

* 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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".