NDC 42537-024 Qore 24 Antimicrobial Hand Purifier
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42537 - Qore Systems Llc
- 42537-024 - Qore 24
Product Packages
NDC Code 42537-024-01
Package Description: 236.59 mL in 1 BOTTLE, SPRAY
NDC Code 42537-024-02
Package Description: 10 mL in 1 BOTTLE, SPRAY
NDC Code 42537-024-03
Package Description: 59.15 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 42537-024?
What are the uses for Qore 24 Antimicrobial Hand Purifier?
Which are Qore 24 Antimicrobial Hand Purifier UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Qore 24 Antimicrobial Hand Purifier 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)
- ALCOHOL (UNII: 3K9958V90M)
- DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)
What is the NDC to RxNorm Crosswalk for Qore 24 Antimicrobial Hand Purifier?
- RxCUI: 1052947 - benzalkonium chloride 0.1 % Topical Spray
- RxCUI: 1052947 - benzalkonium chloride 1 MG/ML Topical Spray
- RxCUI: 1302627 - Qore-24 0.1 % Topical Spray
- RxCUI: 1302627 - benzalkonium chloride 1 MG/ML Topical Spray [Qore-24]
- RxCUI: 1302627 - Qore-24 1 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".