NDC 79247-812 Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79247 - Ivy Rose Inc.
- 79247-812 - Sanitizing Wipes
Product Packages
NDC Code 79247-812-01
Package Description: 183 g in 1 BOX
NDC Code 79247-812-02
Package Description: 122 g in 1 BOX
NDC Code 79247-812-03
Package Description: 338 g in 1 BOX
NDC Code 79247-812-04
Package Description: 540 g in 1 BOX
Product Details
What is NDC 79247-812?
What are the uses for Sanitizing Wipes?
Which are Sanitizing Wipes UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Sanitizing 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE (UNII: V5VD430YW9)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRI-N-BUTYL PHOSPHATE (UNII: 95UAS8YAF5)
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Sanitizing Wipes?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
* 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".