NDC 81496-001 Anmeikang Alcohol Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 81496-001-01
Package Description: 10 CLOTH in 1 BAG
NDC Code 81496-001-02
Package Description: 20 CLOTH in 1 BAG
NDC Code 81496-001-03
Package Description: 22 CLOTH in 1 BAG
NDC Code 81496-001-04
Package Description: 30 CLOTH in 1 BAG
NDC Code 81496-001-05
Package Description: 40 CLOTH in 1 BAG
NDC Code 81496-001-06
Package Description: 50 CLOTH in 1 BAG
NDC Code 81496-001-07
Package Description: 60 CLOTH in 1 BAG
NDC Code 81496-001-08
Package Description: 70 CLOTH in 1 BAG
NDC Code 81496-001-09
Package Description: 80 CLOTH in 1 BAG
NDC Code 81496-001-10
Package Description: 100 CLOTH in 1 BAG
NDC Code 81496-001-11
Package Description: 120 CLOTH in 1 BAG
Product Details
What is NDC 81496-001?
What are the uses for Anmeikang Alcohol Wipes?
Which are Anmeikang Alcohol Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Anmeikang Alcohol 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- 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".