NDC 79208-001 Anti-microbial Alcohol Free Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79208 - Ultra Chem Labs
- 79208-001 - Anti-microbial Alcohol Free Hand Sanitizer
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?
What are the uses for Anti-microbial Alcohol Free Hand Sanitizer?
Which are Anti-microbial Alcohol Free Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
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[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".