NDC 78941-001 Mpulse Antimicrobial Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78941 - Antimicrobial Solutions, Llc
- 78941-001 - Mpulse Antimicrobial Hand Sanitizer
Product Packages
NDC Code 78941-001-01
Package Description: .059 L in 1 BOTTLE
NDC Code 78941-001-02
Package Description: .236 L in 1 BOTTLE
NDC Code 78941-001-03
Package Description: .355 L in 1 BOTTLE
NDC Code 78941-001-04
Package Description: .473 L in 1 BOTTLE
NDC Code 78941-001-05
Package Description: .946 L in 1 BOTTLE
NDC Code 78941-001-06
Package Description: 3.785 L in 1 JUG
NDC Code 78941-001-07
Package Description: 18.927 L in 1 JUG
NDC Code 78941-001-08
Package Description: 208.198 L in 1 DRUM
NDC Code 78941-001-09
Package Description: 1040.99 L in 1 CONTAINER
Product Details
What is NDC 78941-001?
What are the uses for Mpulse Antimicrobial Hand Sanitizer?
Which are Mpulse Antimicrobial 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 Mpulse Antimicrobial 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:
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
What is the NDC to RxNorm Crosswalk for Mpulse Antimicrobial Hand Sanitizer?
- RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
- RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
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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".