NDC 51350-005 Relovox
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51350-005?
What are the uses for Relovox?
Which are Relovox 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 Relovox 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)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ZINC ACETATE (UNII: FM5526K07A)
- ALCOHOL (UNII: 3K9958V90M)
- ALOE (UNII: V5VD430YW9)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CASTOR OIL (UNII: D5340Y2I9G)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SALICYL ALCOHOL (UNII: FA1N0842KB)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
What is the NDC to RxNorm Crosswalk for Relovox?
- RxCUI: 1094744 - Relovox 2.5 % Medicated Liquid Soap
- RxCUI: 1094744 - benzoyl peroxide 25 MG/ML Medicated Liquid Soap [Relovox]
- RxCUI: 1094744 - Relovox 2.5 % Topical Emulsion
- RxCUI: 1094744 - Relovox 25 MG/ML Medicated Liquid Soap
- RxCUI: 845836 - benzoyl peroxide 2.5 % 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".