NDC 63691-013 Home 360 Ultra Dish Detergent Green Apple Scent
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63691-013?
What are the uses for Home 360 Ultra Dish Detergent Green Apple Scent?
Which are Home 360 Ultra Dish Detergent Green Apple Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Home 360 Ultra Dish Detergent Green Apple Scent 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)
- TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- ALCOHOL (UNII: 3K9958V90M)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)
- METHYL PALMITATE (UNII: DPY8VCM98I)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SULISOBENZONE (UNII: 1W6L629B4K)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Home 360 Ultra Dish Detergent Green Apple Scent?
- 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".