NDC 78833-010 Disinfectant Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 78833 - Mb Diversity
- 78833-010 - Disinfectant Wipes
Product Packages
NDC Code 78833-010-01
Package Description: 480 mL in 1 CYLINDER
Product Details
What is NDC 78833-010?
What are the uses for Disinfectant Wipes?
Which are Disinfectant Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Disinfectant Wipes 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:
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- CITRONELLAL (UNII: QB99VZZ7GZ)
- .ALPHA.-PINENE (UNII: JPF3YI7O34)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- LINALYL ACETATE (UNII: 5K47SSQ51G)
- MYRCENE (UNII: 3M39CZS25B)
- LIMONENE DIEPOXIDE (UNII: M6TUW5WEJ9)
- 2-METHOXY-1-PROPANOL (UNII: 18B570XOYF)
- CITRAL (UNII: T7EU0O9VPP)
- 4-METHYL-1,4-PENTANEDIYL DIMETHACRYLATE (UNII: 3BHT04VYO9)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- LAURETH-9 PHOSPHATE (UNII: 0N8G76HI1O)
- .BETA.-PINENE (UNII: 4MS8VHZ1HJ)
- TERPINOLENE (UNII: N9830X5KSL)
* 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".