NDC 80404-301 Wipe Out Antibacterial Wipes Fresh Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 80404-301-01
Package Description: 1 CLOTH in 1 BAG
NDC Code 80404-301-02
Package Description: 10 CLOTH in 1 BAG
NDC Code 80404-301-03
Package Description: 20 CLOTH in 1 BAG
NDC Code 80404-301-04
Package Description: 40 CLOTH in 1 BAG
NDC Code 80404-301-05
Package Description: 60 CLOTH in 1 BAG
NDC Code 80404-301-06
Package Description: 80 CLOTH in 1 BAG
NDC Code 80404-301-07
Package Description: 100 CLOTH in 1 BAG
NDC Code 80404-301-08
Package Description: 120 CLOTH in 1 BAG
NDC Code 80404-301-09
Package Description: 200 CLOTH in 1 BAG
NDC Code 80404-301-10
Package Description: 400 CLOTH in 1 BAG
NDC Code 80404-301-11
Package Description: 500 CLOTH in 1 BAG
NDC Code 80404-301-12
Package Description: 600 CLOTH in 1 BAG
NDC Code 80404-301-13
Package Description: 800 CLOTH in 1 BAG
NDC Code 80404-301-14
Package Description: 1000 CLOTH in 1 BAG
Product Details
What is NDC 80404-301?
What are the uses for Wipe Out Antibacterial Wipes Fresh Scent?
Which are Wipe Out Antibacterial Wipes Fresh Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Wipe Out Antibacterial Wipes Fresh Scent 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Wipe Out Antibacterial Wipes Fresh Scent?
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
- RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM 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".