NDC 21749-358 Purell Hand Sanitizing Wipes Fresh Citrus Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21749 - Gojo Industries, Inc.
- 21749-358 - Purell Hand Sanitizing Wipes Fresh Citrus Scent
Product Packages
NDC Code 21749-358-40
Package Description: 40 LIQUID in 1 PACKAGE
Product Details
What is NDC 21749-358?
What are the uses for Purell Hand Sanitizing Wipes Fresh Citrus Scent?
Which are Purell Hand Sanitizing Wipes Fresh Citrus Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Purell Hand Sanitizing Wipes Fresh Citrus Scent 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)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Purell Hand Sanitizing Wipes Fresh Citrus Scent?
- 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".