NDC 79310-306 Sterizar Advanced Barrier Control Bactericidal Hand Sanitizer Mist
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79310 - Unicorn Media Partners Llc
- 79310-306 - Sterizar
Product Packages
NDC Code 79310-306-20
Package Description: 1000 mL in 1 BOTTLE, SPRAY
NDC Code 79310-306-21
Package Description: 5000 mL in 1 BOTTLE, PUMP
NDC Code 79310-306-22
Package Description: 500 mL in 1 BOTTLE, SPRAY
NDC Code 79310-306-23
Package Description: 100 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 79310-306?
What are the uses for Sterizar Advanced Barrier Control Bactericidal Hand Sanitizer Mist?
Which are Sterizar Advanced Barrier Control Bactericidal Hand Sanitizer Mist UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Sterizar Advanced Barrier Control Bactericidal Hand Sanitizer Mist 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:
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- SODIUM ETHASULFATE (UNII: 12838560LI)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Sterizar Advanced Barrier Control Bactericidal Hand Sanitizer Mist?
- RxCUI: 2462802 - benzalkonium chloride 1.6 % Topical Spray
- RxCUI: 2462802 - benzalkonium chloride 16 MG/ML Topical Spray
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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".