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  4. NDC Product Code: 78003-120 Dermaphex Hand Sanitizer

NDC 78003-120 Dermaphex Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78003-120?
  4. Dermaphex Hand Sanitizer 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:
78003-120
Proprietary Name:
Dermaphex Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aphex Biocleanse Systems, Inc
Labeler Code:
78003
Product Label ID:
a8c90a99-0e22-5ea1-e053-2a95a90a4a3e
Start Marketing Date: [9]
06-01-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78003-120-70

Package Description: 208000 mL in 1 DRUM

NDC Code 78003-120-80

Package Description: 1054000 mL in 1 CONTAINER

Product Details

What is NDC 78003-120?

The NDC code 78003-120 is assigned by the FDA to the product Dermaphex Hand Sanitizer which is product labeled by Aphex Biocleanse Systems, Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 78003-120-70 208000 ml in 1 drum , 78003-120-80 1054000 ml in 1 container . 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 Dermaphex Hand Sanitizer?

Uses: For hand sanitizing. Helps prevent the risk and spread of infection as well as communicable diseases by killing germs that reside on the surface of the skin.

Which are Dermaphex Hand Sanitizer UNII Codes?

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

Which are Dermaphex Hand Sanitizer 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".