NDC 78411-001 Hand Sanitizer Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 78411-001-01
Package Description: 1 POUCH in 1 BAG / 3 g in 1 POUCH
NDC Code 78411-001-02
Package Description: 10 POUCH in 1 BAG / 30 g in 1 POUCH
NDC Code 78411-001-03
Package Description: 15 POUCH in 1 BAG / 45 g in 1 POUCH
NDC Code 78411-001-04
Package Description: 20 POUCH in 1 BAG / 60 g in 1 POUCH
NDC Code 78411-001-05
Package Description: 100 POUCH in 1 BOX / 300 g in 1 POUCH
NDC Code 78411-001-06
Package Description: 60 POUCH in 1 BAG / 180 g in 1 POUCH
NDC Code 78411-001-07
Package Description: 80 POUCH in 1 BAG / 240 g in 1 POUCH
NDC Code 78411-001-08
Package Description: 600 POUCH in 1 BAG / 1800 g in 1 POUCH
NDC Code 78411-001-09
Package Description: 100 POUCH in 1 PAIL / 170 g in 1 POUCH
NDC Code 78411-001-10
Package Description: 160 POUCH in 1 PAIL / 272 g in 1 POUCH
NDC Code 78411-001-11
Package Description: 250 POUCH in 1 PAIL / 425 g in 1 POUCH
NDC Code 78411-001-12
Package Description: 280 POUCH in 1 PAIL / 476 g in 1 POUCH
Product Details
What is NDC 78411-001?
What are the uses for Hand Sanitizer Wipes?
Which are Hand Sanitizer Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer 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:
- WATER (UNII: 059QF0KO0R)
* 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".