NDC 79795-003 Alcohol Wipes (75% Alcohol)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 79795-003-01
Package Description: 3 CLOTH in 1 BAG
NDC Code 79795-003-02
Package Description: 5 CLOTH in 1 BAG
NDC Code 79795-003-03
Package Description: 10 CLOTH in 1 BAG
NDC Code 79795-003-04
Package Description: 20 CLOTH in 1 BAG
NDC Code 79795-003-05
Package Description: 50 CLOTH in 1 BAG
NDC Code 79795-003-06
Package Description: 80 CLOTH in 1 BAG
NDC Code 79795-003-07
Package Description: 75 CLOTH in 1 BOX
NDC Code 79795-003-08
Package Description: 80 CLOTH in 1 BOX
NDC Code 79795-003-09
Package Description: 100 CLOTH in 1 BOX
NDC Code 79795-003-10
Package Description: 150 CLOTH in 1 BOX
NDC Code 79795-003-11
Package Description: 160 CLOTH in 1 BOX
NDC Code 79795-003-12
Package Description: 200 CLOTH in 1 BOX
NDC Code 79795-003-13
Package Description: 600 CLOTH in 1 BOX
NDC Code 79795-003-14
Package Description: 800 CLOTH in 1 BOX
NDC Code 79795-003-15
Package Description: 1000 CLOTH in 1 BOX
NDC Code 79795-003-16
Package Description: 1200 CLOTH in 1 BOX
Product Details
What is NDC 79795-003?
What are the uses for Alcohol Wipes (75% Alcohol)?
Which are Alcohol Wipes (75% Alcohol) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Alcohol Wipes (75% Alcohol) 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".