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  4. NDC Product Code: 76315-1017 Fresh Foam Disinfectant

NDC 76315-1017 Fresh Foam Disinfectant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76315-1017?
  4. Fresh Foam Disinfectant 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:
76315-1017
Proprietary Name:
Fresh Foam Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Devere Company, Inc.
Labeler Code:
76315
Product Label ID:
f5c2f152-c124-4eaa-87f6-b58c6478bfc2
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 76315-1017?

The NDC code 76315-1017 is assigned by the FDA to the product Fresh Foam Disinfectant which is product labeled by Devere Company, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 76315-1017-1 3.8 l in 1 jug , 76315-1017-2 1 l in 1 cartridge . 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 Fresh Foam Disinfectant?

Directions1. Wet hands with water2. Apply FRESH FOAM DISINFEFCTANT SOAP to hands3. Rub hands together to spread lather4. Rinse hands and dry thoroughly

Which are Fresh Foam Disinfectant UNII Codes?

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

Which are Fresh Foam Disinfectant 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 Fresh Foam Disinfectant?

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: 1996972 - chloroxylenol 0.4 % / isopropyl alcohol 1 % Medicated Liquid Soap
  • RxCUI: 1996972 - chloroxylenol 4 MG/ML / isopropyl alcohol 10 MG/ML Medicated Liquid Soap

* 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".