NDC 79795-001 Antibacterial Wipes (75% Alcohol)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79795 - Nantong Guarder Medical Technology Co.,ltd.
- 79795-001 - Antibacterial Wipes (75% Alcohol)
- 79795-001-01
- 79795-001-02
- 79795-001-03
- 79795-001-04
- 79795-001-05
- 79795-001-06
- 79795-001-07
- 79795-001-08
- 79795-001-09
- 79795-001-10
- 79795-001-11
- 79795-001-12
- 79795-001-13
- 79795-001-14
- 79795-001-15
- 79795-001-16
- 79795-001-17
- 79795-001-18
- 79795-001-19
- 79795-001-20
- 79795-001-21
- 79795-001-22
- 79795-001-23
- 79795-001-24
- 79795-001-25
- 79795-001-26
- 79795-001-27
- 79795-001-28
- 79795-001-29
- 79795-001-30
- 79795-001-31
- 79795-001-32
- 79795-001-33
- 79795-001 - Antibacterial Wipes (75% Alcohol)
Product Packages
NDC Code 79795-001-01
Package Description: 1 CLOTH in 1 BAG
NDC Code 79795-001-02
Package Description: 5 CLOTH in 1 BAG
NDC Code 79795-001-03
Package Description: 10 CLOTH in 1 BAG
NDC Code 79795-001-04
Package Description: 20 CLOTH in 1 BAG
NDC Code 79795-001-05
Package Description: 50 CLOTH in 1 BAG
NDC Code 79795-001-06
Package Description: 80 CLOTH in 1 BAG
NDC Code 79795-001-07
Package Description: 100 CLOTH in 1 BAG
NDC Code 79795-001-08
Package Description: 70 CLOTH in 1 BOX
NDC Code 79795-001-09
Package Description: 80 CLOTH in 1 BOX
NDC Code 79795-001-10
Package Description: 85 CLOTH in 1 BOX
NDC Code 79795-001-11
Package Description: 100 CLOTH in 1 BOX
NDC Code 79795-001-12
Package Description: 120 CLOTH in 1 BOX
NDC Code 79795-001-13
Package Description: 160 CLOTH in 1 BOX
NDC Code 79795-001-14
Package Description: 400 CLOTH in 1 BOX
NDC Code 79795-001-15
Package Description: 500 CLOTH in 1 BOX
NDC Code 79795-001-16
Package Description: 800 CLOTH in 1 BOX
NDC Code 79795-001-17
Package Description: 900 CLOTH in 1 BOX
NDC Code 79795-001-18
Package Description: 1000 CLOTH in 1 BOX
NDC Code 79795-001-19
Package Description: 1150 CLOTH in 1 BOX
NDC Code 79795-001-20
Package Description: 1200 CLOTH in 1 BOX
NDC Code 79795-001-21
Package Description: 70 CLOTH in 1 PACKAGE
NDC Code 79795-001-22
Package Description: 80 CLOTH in 1 PACKAGE
NDC Code 79795-001-23
Package Description: 85 CLOTH in 1 PACKAGE
NDC Code 79795-001-24
Package Description: 100 CLOTH in 1 PACKAGE
NDC Code 79795-001-25
Package Description: 120 CLOTH in 1 PACKAGE
NDC Code 79795-001-26
Package Description: 160 CLOTH in 1 PACKAGE
NDC Code 79795-001-27
Package Description: 400 CLOTH in 1 PACKAGE
NDC Code 79795-001-28
Package Description: 500 CLOTH in 1 PACKAGE
NDC Code 79795-001-29
Package Description: 800 CLOTH in 1 PACKAGE
NDC Code 79795-001-30
Package Description: 900 CLOTH in 1 PACKAGE
NDC Code 79795-001-31
Package Description: 1000 CLOTH in 1 PACKAGE
NDC Code 79795-001-32
Package Description: 1150 CLOTH in 1 PACKAGE
NDC Code 79795-001-33
Package Description: 1200 CLOTH in 1 PACKAGE
Product Details
What is NDC 79795-001?
What are the uses for Antibacterial Wipes (75% Alcohol)?
Which are Antibacterial 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 Antibacterial 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".