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  4. NDC Product Code: 69329-025 Releevia

NDC 69329-025 Releevia

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69329-025?
  4. Releevia 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:
69329-025
Proprietary Name:
Releevia
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Patchwerx Labs, Inc
Labeler Code:
69329
Product Label ID:
07eaac2c-60ad-578b-e054-00144ff8d46c
Start Marketing Date: [9]
11-17-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69329-025-05

Package Description: 5 PATCH in 1 CARTON / 100 g in 1 PATCH

NDC Code 69329-025-15

Package Description: 15 PATCH in 1 CARTON / 100 g in 1 PATCH

Product Details

What is NDC 69329-025?

The NDC code 69329-025 is assigned by the FDA to the product Releevia which is product labeled by Patchwerx Labs, Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69329-025-05 5 patch in 1 carton / 100 g in 1 patch, 69329-025-15 15 patch in 1 carton / 100 g in 1 patch. 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 Releevia?

Releevia Patch is indicated for the temporary relief of minor aches and muscle pains associated with arthritis, simple backache, strains, muscle soreness and stiffness.Releevia Patch is an external analgesic/counterirritant.

Which are Releevia UNII Codes?

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

Which are Releevia 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 Releevia?

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: 1300889 - capsaicin 0.0375 % / menthol 5 % Medicated Patch
  • RxCUI: 1300889 - capsaicin 0.000375 MG/MG / menthol 0.05 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".