NDC 50544-152 Acne Wipeout All Day Breakout Control
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50544 - University Medical Pharmaceuticals Corp.
- 50544-152 - Acne Wipeout All Day Breakout Control
Product Packages
NDC Code 50544-152-00
Package Description: 1 TUBE in 1 CARTON / 60 mL in 1 TUBE
Product Details
What is NDC 50544-152?
What are the uses for Acne Wipeout All Day Breakout Control?
Which are Acne Wipeout All Day Breakout Control 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 All Day Breakout Control 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)
What is the NDC to RxNorm Crosswalk for Acne Wipeout All Day Breakout Control?
- RxCUI: 308693 - benzoyl peroxide 5 % Topical Cream
- RxCUI: 308693 - benzoyl peroxide 50 MG/ML Topical Cream
* Please review the disclaimer below.
Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
[Learn More]
* 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".