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  4. NDC Product Code: 47219-341 Qpr Quick Pain Relief

NDC 47219-341 Qpr Quick Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 47219-341?
  4. Qpr Quick Pain Relief Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
47219-341
Proprietary Name:
Qpr Quick Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nutra Pharma Corporation
Labeler Code:
47219
Product Label ID:
cd4abf5a-8862-4fcd-9101-a8625e3e71c7
Start Marketing Date: [9]
09-15-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 47219-341-02

Package Description: 60 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 47219-341?

The NDC code 47219-341 is assigned by the FDA to the product Qpr Quick Pain Relief which is product labeled by Nutra Pharma Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 47219-341-02 60 ml in 1 bottle, 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 Qpr Quick Pain Relief?

Remove protective wrapping Liberally apply gel to the affected area and rub into jointsUse 3-4 times per day for the first week. Use as needed thereafter to relieve discomfortAllow several days for drug to take maximum effect

Which are Qpr Quick Pain Relief UNII Codes?

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

Which are Qpr Quick Pain 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:

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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".