NDC 54340-271 Dial Antibacterial Bar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54340 - The Dial Corporation, A Henkel Company
- 54340-271 - Dial Antibacterial Bar
Product Packages
NDC Code 54340-271-01
Package Description: 180 g in 1 CELLO PACK
NDC Code 54340-271-02
Package Description: 339 g in 1 CELLO PACK
NDC Code 54340-271-03
Package Description: 452 g in 1 CELLO PACK
NDC Code 54340-271-04
Package Description: 678 g in 1 CELLO PACK
NDC Code 54340-271-05
Package Description: 540 g in 1 CELLO PACK
NDC Code 54340-271-06
Package Description: 904 g in 1 CELLO PACK
NDC Code 54340-271-07
Package Description: 1130 g in 1 CELLO PACK
NDC Code 54340-271-08
Package Description: 1080 g in 1 CELLO PACK
Product Details
What is NDC 54340-271?
What are the uses for Dial Antibacterial Bar?
Which are Dial Antibacterial Bar UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dial Antibacterial Bar 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 TALLOWATE, BEEF (UNII: 07RIK6QMEW)
What is the NDC to RxNorm Crosswalk for Dial Antibacterial Bar?
- RxCUI: 1926450 - benzalkonium chloride 0.1 % Medicated Bar Soap
- RxCUI: 1926450 - benzalkonium chloride 0.001 MG/MG Medicated Bar Soap
* Please review the disclaimer below.
[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".