NDC 50988-196 Antibacterial Foaming Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 50988-196?
What are the uses for Antibacterial Foaming Hand Sanitizer?
Which are Antibacterial Foaming Hand Sanitizer 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 Sanitizer 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)
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
- SULISOBENZONE (UNII: 1W6L629B4K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Antibacterial Foaming Hand Sanitizer?
- RxCUI: 1047451 - benzalkonium chloride 0.11 % Topical Foam
- RxCUI: 1047451 - benzalkonium chloride 1.1 MG/ML Topical Foam
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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".