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NDC 77368-902 Durokleen Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77368-902?
  4. Durokleen 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:
77368-902
Proprietary Name:
Durokleen Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nugentec
Labeler Code:
77368
Product Label ID:
b8e9f88a-d086-98a2-e053-2a95a90a9666
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 77368-902?

The NDC code 77368-902 is assigned by the FDA to the product Durokleen Sanitizer which is product labeled by Nugentec. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 77368-902-01 3786 ml in 1 bottle , 77368-902-02 60 ml in 1 bottle, spray , 77368-902-05 18927 ml in 1 bottle , 77368-902-10 1000 ml in 1 bottle , 77368-902-75 750 ml in 1 bottle, spray . 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 Durokleen Sanitizer?

Spray product on hands to cover and wet all surfaces. Rub thoroughly. Allow to dry without wipingSupervise children under 6 years of age when using this product to avoid swallowing.

Which are Durokleen Sanitizer UNII Codes?

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

Which are Durokleen 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:

  • DIMETHYLTETRADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: N7BH1NTV97)
  • WATER (UNII: 059QF0KO0R)

* 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".