NDC 71120-111 Durisan Hand Sanitizer Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71120 - Sanit Technologies Llc
- 71120-111 - Durisan Hand Sanitizer Wipes
Product Packages
NDC Code 71120-111-01
Package Description: 160 mL in 1 CONTAINER
NDC Code 71120-111-02
Package Description: 80 mL in 1 CONTAINER
NDC Code 71120-111-03
Package Description: 240 mL in 1 CONTAINER
Product Details
What is NDC 71120-111?
What are the uses for Durisan Hand Sanitizer Wipes?
Which are Durisan Hand Sanitizer 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 Durisan Hand Sanitizer 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)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
- DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
- GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
What is the NDC to RxNorm Crosswalk for Durisan Hand Sanitizer 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".