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  4. NDC Product Code: 50452-773 Pure Foam

NDC 50452-773 Pure Foam

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50452-773?
  4. Pure Foam 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:
50452-773
Proprietary Name:
Pure Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Phoenix Research Industries, Inc.
Labeler Code:
50452
Product Label ID:
a2f9014c-0497-4be7-9e78-21506b4db8fd
Start Marketing Date: [9]
01-31-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50452-773-25

Package Description: 199 g in 1 CAN

NDC Code 50452-773-26

Package Description: 454 g in 1 CAN

Product Details

What is NDC 50452-773?

The NDC code 50452-773 is assigned by the FDA to the product Pure Foam which is product labeled by Phoenix Research Industries, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 50452-773-25 199 g in 1 can , 50452-773-26 454 g in 1 can . 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 Pure Foam?

For hand-washing to decrease bacteria on the skin, only when water is not available

Which are Pure Foam UNII Codes?

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

Which are Pure Foam 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 Pure Foam?

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".