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  4. NDC Product Code: 40096-0802 Tough Guy Hand Sanitizer Wipes Tough Guy

NDC 40096-0802 Tough Guy Hand Sanitizer Wipes Tough Guy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 40096-0802?
  4. Tough Guy Hand Sanitizer Wipes Tough Guy 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:
40096-0802
Proprietary Name:
Tough Guy Hand Sanitizer Wipes Tough Guy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
W.w. Grainger, Inc.
Labeler Code:
40096
Product Label ID:
119fbc90-1064-4b7d-af06-96a206030d5c
Start Marketing Date: [9]
03-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 40096-0802-0

Package Description: 4 mL in 1 PACKET

NDC Code 40096-0802-1

Package Description: 438 mL in 1 CONTAINER

NDC Code 40096-0802-2

Package Description: 77 mL in 1 PACKAGE

NDC Code 40096-0802-3

Package Description: 206 mL in 1 CONTAINER

NDC Code 40096-0802-4

Package Description: 619 mL in 1 CONTAINER

NDC Code 40096-0802-5

Package Description: 1134 mL in 1 CONTAINER

NDC Code 40096-0802-6

Package Description: 1247 mL in 1 CONTAINER

Product Details

What is NDC 40096-0802?

The NDC code 40096-0802 is assigned by the FDA to the product Tough Guy Hand Sanitizer Wipes Tough Guy which is product labeled by W.w. Grainger, Inc.. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 40096-0802-0 4 ml in 1 packet , 40096-0802-1 438 ml in 1 container , 40096-0802-2 77 ml in 1 package , 40096-0802-3 206 ml in 1 container , 40096-0802-4 619 ml in 1 container , 40096-0802-5 1134 ml in 1 container , 40096-0802-6 1247 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 Tough Guy Hand Sanitizer Wipes Tough Guy?

This product is used as UsesFor hand washing to decrease bacteria on skin.Recommended for repeated use.

Which are Tough Guy Hand Sanitizer Wipes Tough Guy UNII Codes?

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

Which are Tough Guy Hand Sanitizer Wipes Tough Guy 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 Tough Guy Hand Sanitizer Wipes Tough Guy?

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: 1038764 - benzalkonium Cl 0.1 % / benzethonium Cl 0.1 % Medicated Pad
  • RxCUI: 1038764 - benzalkonium chloride 1 MG/ML / benzethonium chloride 1 MG/ML Medicated Pad
  • RxCUI: 1038764 - benzalkonium chloride 0.1 % / benzethonium chloride 0.1 % Medicated Pad

* 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".