NDC 76273-001 Antibacterial Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76273 - Mayborn Usa, Inc.
- 76273-001 - Antibacterial Hand
Product Packages
NDC Code 76273-001-01
Package Description: 50 mL in 1 BOTTLE, PLASTIC
NDC Code 76273-001-02
Package Description: 150 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 76273-001?
What are the uses for Antibacterial Hand?
Which are Antibacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Antibacterial Hand 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)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
- LACTIC ACID (UNII: 33X04XA5AT)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand?
- RxCUI: 1049228 - benzalkonium chloride 0.1 % Topical Gel
- RxCUI: 1049228 - benzalkonium chloride 0.001 MG/MG Topical Gel
* 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".