NDC 51053-500 Alcohol Free Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51053 - Sanihealth Products Corporation
- 51053-500 - Alcohol Free Hand Sanitizer
Product Packages
NDC Code 51053-500-10
Package Description: 1000 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 51053-500?
What are the uses for Alcohol Free Hand Sanitizer?
Which are Alcohol Free Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Alcohol Free Hand Sanitizer?
- RxCUI: 1046310 - benzalkonium chloride 0.12 % Topical Foam
- RxCUI: 1046310 - benzalkonium chloride 1.2 MG/ML Topical Foam
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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".