NDC 79846-151 Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79846 - Jintu Handicraft Factory
- 79846-151 - Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride)
Product Packages
NDC Code 79846-151-05
Package Description: 10 CLOTH in 1 POUCH
NDC Code 79846-151-21
Package Description: 50 CLOTH in 1 POUCH
NDC Code 79846-151-23
Package Description: 60 CLOTH in 1 POUCH
NDC Code 79846-151-25
Package Description: 72 CLOTH in 1 POUCH
NDC Code 79846-151-27
Package Description: 80 CLOTH in 1 POUCH
NDC Code 79846-151-31
Package Description: 100 CLOTH in 1 POUCH
NDC Code 79846-151-50
Package Description: 100 CLOTH in 1 PAIL
NDC Code 79846-151-52
Package Description: 120 CLOTH in 1 PAIL
NDC Code 79846-151-56
Package Description: 160 CLOTH in 1 PAIL
NDC Code 79846-151-58
Package Description: 180 CLOTH in 1 PAIL
NDC Code 79846-151-60
Package Description: 200 CLOTH in 1 PAIL
NDC Code 79846-151-90
Package Description: 500 CLOTH in 1 PAIL
Product Details
What is NDC 79846-151?
What are the uses for Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride)?
Which are Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride) UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride) 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)
What is the NDC to RxNorm Crosswalk for Antiseptic Sanitizing Wipes (0.13% Benzalkonium Chloride)?
- 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
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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".