NDC 54868-2656 Panoxyl
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2656 - Panoxyl
Product Characteristics
Product Packages
NDC Code 54868-2656-0
Package Description: 1 SOAP in 1 CARTON
Product Details
What is NDC 54868-2656?
What are the uses for Panoxyl?
Which are Panoxyl UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Panoxyl 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:
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- LACTIC ACID (UNII: 33X04XA5AT)
- MINERAL OIL (UNII: T5L8T28FGP)
- POTASSIUM PHOSPHATE (UNII: B7862WZ632)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Panoxyl?
- RxCUI: 308685 - benzoyl peroxide 10 % Medicated Bar Soap
- RxCUI: 308685 - benzoyl peroxide 0.1 MG/MG Medicated Bar Soap
- RxCUI: 308692 - benzoyl peroxide 5 % Medicated Bar Soap
- RxCUI: 308692 - benzoyl peroxide 0.05 MG/MG Medicated Bar 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".