NDC 63691-024 Exchange Select Ultra Citrus Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63691 - Sun Products Corporation
- 63691-024 - Exchange Select Ultra Citrus Scent
Product Packages
NDC Code 63691-024-12
Package Description: 591 mL in 1 BOTTLE
Product Details
What is NDC 63691-024?
What are the uses for Exchange Select Ultra Citrus Scent?
Which are Exchange Select Ultra Citrus Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Exchange Select Ultra Citrus 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)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- ALCOHOL (UNII: 3K9958V90M)
- DISODIUM 2-SULFOPALMITATE (UNII: VS9295575T)
- METHYL PALMITATE (UNII: DPY8VCM98I)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SULISOBENZONE (UNII: 1W6L629B4K)
- D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
What is the NDC to RxNorm Crosswalk for Exchange Select Ultra Citrus Scent?
- RxCUI: 1039078 - triclosan 0.1 % Medicated Liquid Soap
- RxCUI: 1039078 - triclosan 1 MG/ML Medicated Liquid 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".