NDC 79208-001 Anti-microbial Alcohol Free Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
79208-001
Proprietary Name:
Anti-microbial Alcohol Free Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ultra Chem Labs
Labeler Code:
79208
Start Marketing Date: [9]
07-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79208-001-01

Package Description: 3785 mg in 1 BOTTLE

NDC Code 79208-001-32

Package Description: 946 mg in 1 BOTTLE

NDC Code 79208-001-50

Package Description: 50 mg in 1 BOTTLE

Product Details

What is NDC 79208-001?

The NDC code 79208-001 is assigned by the FDA to the product Anti-microbial Alcohol Free Hand Sanitizer which is product labeled by Ultra Chem Labs. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 79208-001-01 3785 mg in 1 bottle , 79208-001-32 946 mg in 1 bottle , 79208-001-50 50 mg 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 Anti-microbial Alcohol Free Hand Sanitizer?

• For hand washing to decrease bacteria on the skin • Recommended for repeated use

Which are Anti-microbial Alcohol Free Hand Sanitizer UNII Codes?

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

Which are Anti-microbial Alcohol Free 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".