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  4. NDC Product Code: 79421-004 American Hand Sanitizer

NDC 79421-004 American Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79421-004?
  4. American 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:
79421-004
Proprietary Name:
American Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
American Hand Sanitizer Llc
Labeler Code:
79421
Product Label ID:
accac7ac-40f5-0f43-e053-2a95a90a821e
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79421-004-01

Package Description: 150 mL in 1 CONTAINER

NDC Code 79421-004-02

Package Description: 3785 mL in 1 JUG

NDC Code 79421-004-03

Package Description: 59 mL in 1 BOTTLE

Product Details

What is NDC 79421-004?

The NDC code 79421-004 is assigned by the FDA to the product American Hand Sanitizer which is product labeled by American Hand Sanitizer Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 79421-004-01 150 ml in 1 container , 79421-004-02 3785 ml in 1 jug , 79421-004-03 59 ml in 1 bottle . 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 American Hand Sanitizer?

Read the entire label before using this product.Pump a small amout of liquid into palm of hand.Rub thoroughly over all surfaces on both hands for 15 seconds

Which are American Hand Sanitizer UNII Codes?

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

Which are American 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".