NDC 59647-750 Antiseptic Towelette
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59647 - Med-nap Llc
- 59647-750 - Antiseptic
Product Packages
NDC Code 59647-750-00
Package Description: 60000 PACKET in 1 CONTAINER / 1.4 mL in 1 PACKET (59647-750-01)
Product Details
What is NDC 59647-750?
What are the uses for Antiseptic Towelette?
Which are Antiseptic Towelette 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 Towelette 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)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- MAGNESIUM CHLORIDE ANHYDROUS (UNII: 59XN63C8VM)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
What is the NDC to RxNorm Crosswalk for Antiseptic Towelette?
- RxCUI: 1043307 - benzalkonium Cl 0.133 % Medicated Pad
- RxCUI: 1043307 - benzalkonium chloride 1.33 MG/ML Medicated Pad
- RxCUI: 1043307 - benzalkonium chloride 0.133 % Medicated Towelette
- RxCUI: 1043307 - benzalkonium chloride 0.133 % 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".