NDC 0519-6262 Cv Medicated
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0519 - Steris Corporation
- 0519-6262 - Cv Medicated
Product Characteristics
Product Packages
NDC Code 0519-6262-87
Package Description: 12 BOTTLE in 1 CASE / 1000 mL in 1 BOTTLE (0519-6262-41)
NDC Code 0519-6262-92
Package Description: 18 BOTTLE in 1 CASE / 444 mL in 1 BOTTLE (0519-6262-13)
NDC Code 0519-6262-94
Package Description: 72 BOTTLE in 1 CASE / 118 mL in 1 BOTTLE (0519-6262-03)
Product Details
What is NDC 0519-6262?
What are the uses for Cv Medicated?
Which are Cv Medicated UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Cv Medicated 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)
- SORBITOL (UNII: 506T60A25R)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)
- GELATIN HYDROLYSATE (PORCINE SKIN, MW 3000) (UNII: 0K9R94573C)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
What is the NDC to RxNorm Crosswalk for Cv Medicated?
- RxCUI: 413247 - triclosan 0.5 % Medicated Liquid Soap
- RxCUI: 413247 - triclosan 5 MG/ML Medicated Liquid Soap
- RxCUI: 413247 - triclosan 0.5 % Foaming Medicated Hand 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".