NDC 63691-014 Publix Ultradish Detergent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63691 - Sun Products Corporation
- 63691-014 - Publix Ultradish Detergent
Product Packages
NDC Code 63691-014-10
Package Description: 709 mL in 1 BOTTLE
Product Details
What is NDC 63691-014?
What are the uses for Publix Ultradish Detergent?
Which are Publix Ultradish Detergent UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Publix Ultradish Detergent 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)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- ALCOHOL (UNII: 3K9958V90M)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SULISOBENZONE (UNII: 1W6L629B4K)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Publix Ultradish Detergent?
- RxCUI: 1039078 - triclosan 0.1 % Medicated Liquid Soap
- RxCUI: 1039078 - triclosan 1 MG/ML Medicated Liquid Soap
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[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".