NDC 50519-221 Sani-gel

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:
Proprietary Name:
Product Type: [3]
Labeler Code:
Start Marketing Date: [9]
Listing Expiration Date: [11]
Exclude Flag: [12]
Code Navigator:

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Product Details

What is NDC 50519-221?

The NDC code 50519-221 is assigned by the FDA to the product Sani-gel which is product labeled by American Industrial Supply, Inc.. The product's dosage form is . The product is distributed in 18 packages with assigned NDC codes 50519-221-01 1200 ml in 1 cartridge , 50519-221-03 350 ml in 1 cartridge , 50519-221-05 540 ml in 1 bottle, plastic , 50519-221-06 1 bag in 1 box / 800 ml in 1 bag, 50519-221-07 700 ml in 1 bag , 50519-221-08 1 bag in 1 box / 1000 ml in 1 bag, 50519-221-09 2000 ml in 1 cartridge , 50519-221-10 1000 ml in 1 cartridge , 50519-221-11 1000 ml in 1 bottle, plastic , 50519-221-12 1000 ml in 1 bag , 50519-221-13 800 ml in 1 bag , 50519-221-14 3785 ml in 1 bottle, plastic , 50519-221-15 946 ml in 1 bottle, plastic , 50519-221-17 532 ml in 1 bottle, plastic , 50519-221-24 118 ml in 1 bottle, plastic , 50519-221-27 800 ml in 1 cartridge , 50519-221-28 149 ml in 1 bottle, plastic , 50519-221-55 208200 ml in 1 drum . 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 Sani-gel?

For hand-washing to decrease bacteria on the skin, only when water is not available

Which are Sani-gel UNII Codes?

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

Which are Sani-gel 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".