NDC 43374-575 Quik San
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 43374-575-10
Package Description: 1000 mL in 1 CARTRIDGE
NDC Code 43374-575-12
Package Description: 1000 mL in 1 BAG
NDC Code 43374-575-13
Package Description: 800 mL in 1 BAG
NDC Code 43374-575-14
Package Description: 3785 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-15
Package Description: 946 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-16
Package Description: 236 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-17
Package Description: 532 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-18
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-24
Package Description: 115 mL in 1 BOTTLE, PLASTIC
NDC Code 43374-575-55
Package Description: 208200 mL in 1 DRUM
Product Details
What is NDC 43374-575?
What are the uses for Quik San?
Which are Quik San UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Quik San 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- 1,3-DIMETHYLOL-5,5-DIMETHYL-HYDANTOIN (UNII: BYR0546TOW)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Quik San?
- RxCUI: 1041869 - benzethonium chloride 0.2 % Topical Foam
- RxCUI: 1041869 - benzethonium chloride 2 MG/ML Topical Foam
* Please review the disclaimer below.
[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".