NDC 79293-001 Antibacterial Wet Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 79293-001-01
Package Description: 200 BAG in 1 CARTON / 10 POUCH in 1 BAG / 48 g in 1 POUCH
NDC Code 79293-001-02
Package Description: 100 BAG in 1 CARTON / 15 POUCH in 1 BAG / 72 g in 1 POUCH
NDC Code 79293-001-03
Package Description: 100 BAG in 1 CARTON / 20 POUCH in 1 BAG / 96 g in 1 POUCH
NDC Code 79293-001-04
Package Description: 80 BAG in 1 CARTON / 25 POUCH in 1 BAG / 120 g in 1 POUCH
NDC Code 79293-001-05
Package Description: 60 BAG in 1 CARTON / 30 POUCH in 1 BAG / 144 g in 1 POUCH
NDC Code 79293-001-06
Package Description: 30 BAG in 1 CARTON / 50 POUCH in 1 BAG / 240 g in 1 POUCH
NDC Code 79293-001-07
Package Description: 30 BAG in 1 CARTON / 60 POUCH in 1 BAG / 288 g in 1 POUCH
NDC Code 79293-001-08
Package Description: 20 BAG in 1 CARTON / 80 POUCH in 1 BAG / 384 g in 1 POUCH
NDC Code 79293-001-09
Package Description: 12 BAG in 1 CARTON / 100 POUCH in 1 BAG / 480 g in 1 POUCH
NDC Code 79293-001-10
Package Description: 10 BAG in 1 CARTON / 120 POUCH in 1 BAG / 576 g in 1 POUCH
NDC Code 79293-001-11
Package Description: 200 BAG in 1 CARTON / 10 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-12
Package Description: 100 BAG in 1 CARTON / 15 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-13
Package Description: 100 BAG in 1 CARTON / 20 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-14
Package Description: 80 BAG in 1 CARTON / 25 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-15
Package Description: 60 BAG in 1 CARTON / 30 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-16
Package Description: 30 BAG in 1 CARTON / 50 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-17
Package Description: 30 BAG in 1 CARTON / 60 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-18
Package Description: 20 BAG in 1 CARTON / 80 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-19
Package Description: 12 BAG in 1 CARTON / 100 PATCH in 1 BAG / 4.8 g in 1 PATCH
NDC Code 79293-001-20
Package Description: 10 BAG in 1 CARTON / 120 PATCH in 1 BAG / 4.8 g in 1 PATCH
Product Details
What is NDC 79293-001?
What are the uses for Antibacterial Wet Wipes?
Which are Antibacterial Wet Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Wet 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Antibacterial Wet Wipes?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
* 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".