NDC 50036-571 Fikes Foaming Anti-microbial Food Service Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50036 - Fikes Northwest, Corp.
- 50036-571 - Fikes Foaming Anti-microbial Food Service Hand Wash
Product Packages
NDC Code 50036-571-05
Package Description: 3785 mL in 1 BOTTLE
Product Details
What is NDC 50036-571?
What are the uses for Fikes Foaming Anti-microbial Food Service Hand Wash?
Which are Fikes Foaming Anti-microbial Food Service Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Fikes Foaming Anti-microbial Food Service Hand Wash 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- TRICLOSAN (UNII: 4NM5039Y5X)
What is the NDC to RxNorm Crosswalk for Fikes Foaming Anti-microbial Food Service Hand Wash?
- RxCUI: 1092578 - chloroxylenol 1.49 % Medicated LIquid Soap
- RxCUI: 1092578 - chloroxylenol 14.9 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".