NDC 74149-034 Antibacterial Hand Sanitizer Cucumber Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 74149 - Yiwu Yangjie Daily Chemicals Co.,ltd.
- 74149-034 - Antibacterial Hand Sanitizer Cucumber Scent
Product Packages
NDC Code 74149-034-01
Package Description: 59 mL in 1 BOTTLE
Product Details
What is NDC 74149-034?
What are the uses for Antibacterial Hand Sanitizer Cucumber Scent?
Which are Antibacterial Hand Sanitizer Cucumber 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 Antibacterial Hand Sanitizer Cucumber 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- 2-HYDROXYETHYL ACRYLATE (UNII: 25GT92NY0C)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand Sanitizer Cucumber Scent?
- RxCUI: 1102185 - benzalkonium chloride 0.1 % Topical Lotion
- RxCUI: 1102185 - benzalkonium chloride 1 MG/ML Topical Lotion
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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".