NDC 80861-003 Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser
Benzoyl Peroxide Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80861 - Acnefree, Llc
- 80861-003 - Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser
Product Packages
NDC Code 80861-003-01
Package Description: 1 KIT in 1 KIT * 118 mL in 1 BOTTLE (80861-004-01)
Product Details
What is NDC 80861-003?
What are the uses for Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser?
Which are Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser 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 Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- CERAMIDE NP (UNII: 4370DF050B)
- CERAMIDE AP (UNII: F1X8L2B00J)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- CERAMIDE 1 (UNII: 5THT33P7X7)
What is the NDC to RxNorm Crosswalk for Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser?
- RxCUI: 845836 - benzoyl peroxide 2.5 % Medicated Liquid Soap
- RxCUI: 845836 - benzoyl peroxide 25 MG/ML Medicated Liquid Soap
* 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.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".