NDC 76772-032 Antibacterial
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What is NDC 76772-032?
What are the uses for Antibacterial?
Which are Antibacterial 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 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- EDETIC ACID (UNII: 9G34HU7RV0)
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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".