NDC 54340-178 Dial Lavender And Twilight Jasmine Antibacterial Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54340 - The Dial Corporation
- 54340-178 - Dial Lavender And Twilight Jasmine Antibacterial Body Wash
Product Packages
NDC Code 54340-178-01
Package Description: 355 mL in 1 BOTTLE, PLASTIC
NDC Code 54340-178-02
Package Description: 532 mL in 1 BOTTLE, PLASTIC
NDC Code 54340-178-03
Package Description: 621 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54340-178?
What are the uses for Dial Lavender And Twilight Jasmine Antibacterial Body Wash?
Which are Dial Lavender And Twilight Jasmine Antibacterial Body Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOSAN (UNII: 4NM5039Y5X)
- TRICLOSAN (UNII: 4NM5039Y5X) (Active Moiety)
Which are Dial Lavender And Twilight Jasmine Antibacterial Body 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- CHLORIDE ION (UNII: Q32ZN48698)
- MORPHOLINE (UNII: 8B2ZCK305O)
- LACTIC ACID (UNII: 33X04XA5AT)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Dial Lavender And Twilight Jasmine Antibacterial Body Wash?
- RxCUI: 1020118 - triclosan 0.15 % Medicated Liquid Soap
- RxCUI: 1020118 - triclosan 1.5 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".