NDC 51209-017 Covex Antibacterial Bar Active Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51209 - Dalan Kimya Endustri Anonim Sirketi
- 51209-017 - Covex Antibacterial Bar Active Protection
Product Packages
NDC Code 51209-017-00
Package Description: 3 PACKAGE in 1 PACKAGE / 115 g in 1 PACKAGE
Product Details
What is NDC 51209-017?
What are the uses for Covex Antibacterial Bar Active Protection?
Which are Covex Antibacterial Bar Active Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Covex Antibacterial Bar Active Protection 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:
- SODIUM TALLOWATE, BEEF (UNII: 07RIK6QMEW)
- SODIUM PALMATE (UNII: S0A6004K3Z)
- WATER (UNII: 059QF0KO0R)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETIDRONIC ACID (UNII: M2F465ROXU)
- DISODIUM DISTYRYLBIPHENYL DISULFONATE (UNII: 81G7704MYR)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- GERANIOL (UNII: L837108USY)
- EUGENOL (UNII: 3T8H1794QW)
What is the NDC to RxNorm Crosswalk for Covex Antibacterial Bar Active Protection?
- RxCUI: 2057666 - benzalkonium chloride 0.13 % Medicated Bar Soap
- RxCUI: 2057666 - benzalkonium chloride 0.0013 MG/MG Medicated Bar Soap
* 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".