NDC 75111-401 Sanitizing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 75111-401-01
Package Description: 80 CLOTH in 1 CANISTER
NDC Code 75111-401-02
Package Description: 90 CLOTH in 1 CANISTER
NDC Code 75111-401-03
Package Description: 100 CLOTH in 1 CANISTER
NDC Code 75111-401-04
Package Description: 50 CLOTH in 1 CANISTER
NDC Code 75111-401-05
Package Description: 60 CLOTH in 1 CANISTER
NDC Code 75111-401-06
Package Description: 70 CLOTH in 1 CANISTER
NDC Code 75111-401-07
Package Description: 120 CLOTH in 1 CANISTER
NDC Code 75111-401-08
Package Description: 160 CLOTH in 1 CANISTER
Product Details
What is NDC 75111-401?
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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
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[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".