NDC 90042-201 Antibacterial Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 90042-201-01
Package Description: 120 CLOTH in 1 BAG
NDC Code 90042-201-02
Package Description: 70 CLOTH in 1 BAG
NDC Code 90042-201-03
Package Description: 50 CLOTH in 1 BAG
NDC Code 90042-201-04
Package Description: 10 CLOTH in 1 BAG
NDC Code 90042-201-05
Package Description: 80 CLOTH in 1 BAG
NDC Code 90042-201-06
Package Description: 100 CLOTH in 1 BAG
NDC Code 90042-201-07
Package Description: 20 CLOTH in 1 BAG
NDC Code 90042-201-08
Package Description: 1 CLOTH in 1 BAG
NDC Code 90042-201-09
Package Description: 200 CLOTH in 1 CANISTER
NDC Code 90042-201-10
Package Description: 180 CLOTH in 1 CANISTER
NDC Code 90042-201-11
Package Description: 160 CLOTH in 1 CANISTER
NDC Code 90042-201-12
Package Description: 120 CLOTH in 1 CANISTER
NDC Code 90042-201-13
Package Description: 100 CLOTH in 1 CANISTER
NDC Code 90042-201-14
Package Description: 80 CLOTH in 1 CANISTER
NDC Code 90042-201-15
Package Description: 75 CLOTH in 1 CANISTER
NDC Code 90042-201-16
Package Description: 60 CLOTH in 1 CANISTER
NDC Code 90042-201-17
Package Description: 250 CLOTH in 1 CANISTER
NDC Code 90042-201-18
Package Description: 300 CLOTH in 1 CANISTER
NDC Code 90042-201-19
Package Description: 500 CLOTH in 1 CANISTER
NDC Code 90042-201-20
Package Description: 800 CLOTH in 1 CANISTER
NDC Code 90042-201-21
Package Description: 1000 CLOTH in 1 CANISTER
NDC Code 90042-201-22
Package Description: 1200 CLOTH in 1 CANISTER
Product Details
What is NDC 90042-201?
What are the uses for Antibacterial Wipes?
Which are Antibacterial Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- DIDECYLDIMONIUM (UNII: Z7F472XQPA) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Wipes 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)
* 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".