NDC 50544-150 Acne Wipeout Clinical Acne System
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 50544-150?
What are the uses for Acne Wipeout Clinical Acne System?
Which are Acne Wipeout Clinical Acne System 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 Acne Wipeout Clinical Acne System 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 C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ALLYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: B9J55EA6QX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- JOJOBA OIL (UNII: 724GKU717M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
What is the NDC to RxNorm Crosswalk for Acne Wipeout Clinical Acne System?
- RxCUI: 308693 - benzoyl peroxide 5 % Topical Cream
- RxCUI: 308693 - benzoyl peroxide 50 MG/ML Topical Cream
- RxCUI: 845836 - benzoyl peroxide 2.5 % Medicated Liquid Soap
- RxCUI: 845836 - benzoyl peroxide 25 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".