NDC 11084-054 Agrobac Foam Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11084 - Deb Usa, Inc.
- 11084-054 - Agrobac Foam Wash
Product Packages
NDC Code 11084-054-20
Package Description: 2000 mL in 1 BOTTLE, PLASTIC
NDC Code 11084-054-27
Package Description: 1000 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11084-054?
What are the uses for Agrobac Foam Wash?
Which are Agrobac Foam Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Agrobac Foam Wash 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Agrobac Foam Wash?
- RxCUI: 1089990 - benzalkonium chloride 1.3 % Medicated Liquid Soap
- RxCUI: 1089990 - benzalkonium chloride 13 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".