NDC 64064-105 Stoko Refresh Food Handler Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64064 - Evonik Stockhausen, Llc
- 64064-105 - Stoko Refresh Food Handler Foam
Product Packages
NDC Code 64064-105-01
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 64064-105?
What are the uses for Stoko Refresh Food Handler Foam?
Which are Stoko Refresh Food Handler Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Stoko Refresh Food Handler Foam 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 CUMENESULFONATE (UNII: 5798KA13PG)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Stoko Refresh Food Handler Foam?
- RxCUI: 413247 - triclosan 0.5 % Medicated Liquid Soap
- RxCUI: 413247 - triclosan 5 MG/ML Medicated Liquid Soap
- RxCUI: 413247 - triclosan 0.5 % 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".