NDC 40099-023 Superguard Antibacterial Liquid Handsoap Coconut
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 40099-023?
What are the uses for Superguard Antibacterial Liquid Handsoap Coconut?
Which are Superguard Antibacterial Liquid Handsoap Coconut UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Superguard Antibacterial Liquid Handsoap Coconut 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:
- STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
- WATER (UNII: 059QF0KO0R)
- SULISOBENZONE (UNII: 1W6L629B4K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- EDETATE SODIUM (UNII: MP1J8420LU)
What is the NDC to RxNorm Crosswalk for Superguard Antibacterial Liquid Handsoap Coconut?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 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".