NDC 74534-014 Disinfectant Liquid Antibacterial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 74534-014-01
Package Description: 500 g in 1 BOTTLE
NDC Code 74534-014-02
Package Description: 300 g in 1 BOTTLE
NDC Code 74534-014-03
Package Description: 200 g in 1 BOTTLE
NDC Code 74534-014-04
Package Description: 100 g in 1 BOTTLE
NDC Code 74534-014-05
Package Description: 120 g in 1 BOTTLE
NDC Code 74534-014-06
Package Description: 250 g in 1 BOTTLE
NDC Code 74534-014-07
Package Description: 1000000 g in 1 BOTTLE
NDC Code 74534-014-08
Package Description: 100000 g in 1 BOTTLE
NDC Code 74534-014-09
Package Description: 50000 g in 1 BOTTLE
NDC Code 74534-014-10
Package Description: 2000 g in 1 BOTTLE
NDC Code 74534-014-11
Package Description: 1000 g in 1 BOTTLE
NDC Code 74534-014-12
Package Description: 600 g in 1 BOTTLE
Product Details
What is NDC 74534-014?
What are the uses for Disinfectant Liquid Antibacterial?
Which are Disinfectant Liquid Antibacterial UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYPOCHLOROUS ACID (UNII: 712K4CDC10)
- HYPOCHLOROUS ACID (UNII: 712K4CDC10) (Active Moiety)
Which are Disinfectant Liquid 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
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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".