NDC 72133-151 Personal Care Antibacterial Hand
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72133 - Delta Brands & Products Llc
- 72133-151 - Personal Care
Product Packages
NDC Code 72133-151-15
Package Description: 444 mL in 1 BOTTLE, PUMP
NDC Code 72133-151-75
Package Description: 221.8 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 72133-151?
What are the uses for Personal Care Antibacterial Hand?
Which are Personal Care Antibacterial Hand UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Personal Care Antibacterial Hand 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Personal Care Antibacterial Hand?
- RxCUI: 413261 - chloroxylenol 0.3 % Medicated Liquid Soap
- RxCUI: 413261 - chloroxylenol 3 MG/ML Medicated Liquid Soap
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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".