NDC 74653-104 Clinicare Pro Surface Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74653 - Meroven Llc
- 74653-104 - Clinicare Pro Surface Sanitizer
Product Packages
NDC Code 74653-104-21
Package Description: 80 mL in 1 BOTTLE
NDC Code 74653-104-22
Package Description: 500 mL in 1 BOTTLE
NDC Code 74653-104-23
Package Description: 1000 mL in 1 BOTTLE
NDC Code 74653-104-24
Package Description: 3000 mL in 1 BOTTLE
NDC Code 74653-104-25
Package Description: 5000 mL in 1 BOTTLE
Product Details
What is NDC 74653-104?
What are the uses for Clinicare Pro Surface Sanitizer?
Which are Clinicare Pro Surface Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- DIDECYLDIMONIUM (UNII: Z7F472XQPA) (Active Moiety)
Which are Clinicare Pro Surface 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- LAURETH-4 (UNII: 6HQ855798J)
- WATER (UNII: 059QF0KO0R)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDE (UNII: GLJ50K866T)
- DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)
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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".