NDC 68071-4393 Rugby Benzoyl Peroxide Acne Medication
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-4393 - Rugby Benzoyl Peroxide
Product Characteristics
Product Packages
NDC Code 68071-4393-1
Package Description: 42.5 mL in 1 BOX
Product Details
What is NDC 68071-4393?
What are the uses for Rugby Benzoyl Peroxide Acne Medication?
Which are Rugby Benzoyl Peroxide Acne Medication 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 Rugby Benzoyl Peroxide Acne Medication 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LAURETH-4 (UNII: 6HQ855798J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Rugby Benzoyl Peroxide Acne Medication?
- RxCUI: 486131 - benzoyl peroxide 10 % Topical Gel
- RxCUI: 486131 - benzoyl peroxide 0.1 MG/MG Topical Gel
* 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".