NDC 41250-187 Antibacterial Foaming Cucumber Melon
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41250 - Meijer Distribution Inc
- 41250-187 - Antibacterial Foaming
Product Packages
NDC Code 41250-187-08
Package Description: 221 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 41250-187?
What are the uses for Antibacterial Foaming Cucumber Melon?
Which are Antibacterial Foaming Cucumber Melon UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Antibacterial Foaming Cucumber Melon 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 LAURETH SULFATE (UNII: BPV390UAP0)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Antibacterial Foaming Cucumber Melon?
- RxCUI: 413249 - triclosan 0.6 % Medicated Liquid Soap
- RxCUI: 413249 - triclosan 6 MG/ML Medicated Liquid Soap
- RxCUI: 413249 - triclosan 0.6 % 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".