NDC 79590-006 Disinfecting Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79590 - Mbs Medical Technologies
- 79590-006 - Disinfecting Wipes
Product Packages
NDC Code 79590-006-00
Package Description: 50 BAG in 1 BOX / 50 NOT APPLICABLE in 1 BAG / 50 g in 1 NOT APPLICABLE
NDC Code 79590-006-01
Package Description: 160 BAG in 1 CARTON / 160 NOT APPLICABLE in 1 BAG / 160 g in 1 NOT APPLICABLE
NDC Code 79590-006-02
Package Description: 65 BAG in 1 CARTON / 65 NOT APPLICABLE in 1 BAG / 65 g in 1 NOT APPLICABLE
NDC Code 79590-006-03
Package Description: 500 BAG in 1 CARTON / 500 NOT APPLICABLE in 1 BAG / 500 g in 1 NOT APPLICABLE
Product Details
What is NDC 79590-006?
What are the uses for Disinfecting Wipes?
Which are Disinfecting 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 Disinfecting 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)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Disinfecting 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".