NDC 42546-016 Benzepro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 42546-016?
What are the uses for Benzepro?
Which are Benzepro 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 Benzepro 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 COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ZINC LACTATE (UNII: 2GXR25858Y)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
What is the NDC to RxNorm Crosswalk for Benzepro?
- RxCUI: 1605441 - Benzepro 6 % Medicated Towelette
- RxCUI: 1605441 - benzoyl peroxide 60 MG/ML Medicated Pad [Benzepro]
- RxCUI: 797704 - benzoyl peroxide 6 % Medicated Pad
- RxCUI: 797704 - benzoyl peroxide 60 MG/ML Medicated Pad
- RxCUI: 797704 - benzoyl peroxide 6 % Towelette
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Patient Education
Benzoyl Peroxide Topical
Benzoyl peroxide is used to treat mild to moderate acne.
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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".