NDC 63002-001 Wsna Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63002 - Advanced Hygienics Llc
- 63002-001 - Wsna Hand Sanitizer
Product Packages
NDC Code 63002-001-99
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 63002-001?
What are the uses for Wsna Hand Sanitizer?
Which are Wsna Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Wsna Hand Sanitizer 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)
- GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
- DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
- POLIHEXANIDE (UNII: 322U039GMF)
- CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
- C12-15 PARETH-7 (UNII: 3XY03A79QH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Wsna Hand Sanitizer?
- RxCUI: 1020365 - benzalkonium chloride 0.13 % Topical Foam
- RxCUI: 1020365 - benzalkonium chloride 1.3 MG/ML Topical Foam
* 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".