NDC 63517-418 Cardinal Health Antimicrobial Soap With Triclosan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63517 - Cardinal Health
- 63517-418 - Cardinal Health Antimicrobial Soap With Triclosan
Product Packages
NDC Code 63517-418-10
Package Description: 1 BAG in 1 BOX / 1000 mL in 1 BAG
NDC Code 63517-418-16
Package Description: 12 BOTTLE, PUMP in 1 CASE / 473 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 63517-418?
What are the uses for Cardinal Health Antimicrobial Soap With Triclosan?
Which are Cardinal Health Antimicrobial Soap With Triclosan UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Cardinal Health Antimicrobial Soap With Triclosan 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCONUT ACID (UNII: 40U37V505D)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- OLEIC ACID (UNII: 2UMI9U37CP)
- MONOETHANOLAMINE (UNII: 5KV86114PT)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CORN OIL (UNII: 8470G57WFM)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Cardinal Health Antimicrobial Soap With Triclosan?
- RxCUI: 260054 - triclosan 0.3 % Medicated Liquid Soap
- RxCUI: 260054 - triclosan 3 MG/ML Medicated Liquid Soap
- RxCUI: 260054 - triclosan 0.3 % 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".