NDC 61619-718 Antimicrobial Foaming Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61619 - A-cute Derm, Incorporated
- 61619-718 - Antimicrobial Foaming Sanitizer
Product Packages
NDC Code 61619-718-32
Package Description: 946 g in 1 BOTTLE
NDC Code 61619-718-37
Package Description: 50 g in 1 BOTTLE
NDC Code 61619-718-70
Package Description: 207 g in 1 BOTTLE
Product Details
What is NDC 61619-718?
What are the uses for Antimicrobial Foaming Sanitizer?
Which are Antimicrobial Foaming Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Antimicrobial Foaming Sanitizer 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:
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- 2-HEXENAL PROPYLENE GLYCOL ACETAL, (1E)- (UNII: ZBS49DF5S4)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
What is the NDC to RxNorm Crosswalk for Antimicrobial Foaming Sanitizer?
- RxCUI: 1041869 - benzethonium chloride 0.2 % Topical Foam
- RxCUI: 1041869 - benzethonium chloride 2 MG/ML Topical Foam
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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".