NDC 54340-243 Dial Antibacterial Hand Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54340 - The Dial Corporation, A Henkel Company
- 54340-243 - Dial Antibacterial Hand Wash
Product Characteristics
Product Packages
NDC Code 54340-243-01
Package Description: 162 mL in 1 BOTTLE, PUMP
NDC Code 54340-243-02
Package Description: 221 mL in 1 BOTTLE, PUMP
NDC Code 54340-243-03
Package Description: 277 mL in 1 BOTTLE, PUMP
NDC Code 54340-243-04
Package Description: 946 mL in 1 BOTTLE, DISPENSING
NDC Code 54340-243-05
Package Description: 1537 mL in 1 BOTTLE, DISPENSING
NDC Code 54340-243-06
Package Description: 3785 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 54340-243?
What are the uses for Dial Antibacterial Hand Wash?
Which are Dial Antibacterial Hand Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Dial Antibacterial Hand 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
What is the NDC to RxNorm Crosswalk for Dial Antibacterial Hand Wash?
- RxCUI: 1053207 - benzethonium chloride 0.1 % Medicated Liquid Soap
- RxCUI: 1053207 - benzethonium chloride 1 MG/ML Medicated Liquid 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".