1. Home
  2. Labeler Index
  3. Nutri-dyn Products Ltd. Dba Professional Health Products
  4. NDC Product Code: 49795-227 Pro-flex

NDC 49795-227 Pro-flex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49795-227?
  4. Pro-flex 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:
49795-227
Proprietary Name:
Pro-flex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nutri-dyn Products Ltd. Dba Professional Health Products
Labeler Code:
49795
Product Label ID:
3ca7e006-069f-4991-b457-6d4501673d78
Start Marketing Date: [9]
02-01-2004
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 49795-227?

The NDC code 49795-227 is assigned by the FDA to the product Pro-flex which is product labeled by Nutri-dyn Products Ltd. Dba Professional Health Products. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 49795-227-01 120 g in 1 jar , 49795-227-02 500 g in 1 bottle, plastic , 49795-227-03 5 g in 1 jar . 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 Pro-flex?

Uses for the temporary relief of minor aches and joint pain associated with backpain, arthritis, strains, bruises and sprains.

Which are Pro-flex UNII Codes?

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

Which are Pro-flex 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 Pro-flex?

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:

* 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".