NDC 50988-290 Antibacterial Foaming Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50988 - Jets, Sets, & Elephants Beauty Corp.
- 50988-290 - Antibacterial Foaming Hand
Product Packages
NDC Code 50988-290-00
Package Description: 295.74 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 50988-290?
What are the uses for Antibacterial Foaming Hand?
Which are Antibacterial Foaming Hand 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 Foaming Hand 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:
- SULISOBENZONE (UNII: 1W6L629B4K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)
- SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Antibacterial Foaming Hand?
- RxCUI: 1242883 - benzalkonium chloride 0.11 % Medicated Liquid Soap
- RxCUI: 1242883 - benzalkonium chloride 1.1 MG/ML Medicated Liquid Soap
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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".