NDC 72934-8022 Benzoyl Peroxide 8% / Niacinamide 4%

Benzoyl Peroxide 8% / Niacinamide 4%

NDC Product Code 72934-8022

NDC Code: 72934-8022

Proprietary Name: Benzoyl Peroxide 8% / Niacinamide 4% What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Benzoyl Peroxide 8% / Niacinamide 4% 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.

NDC Code Structure

  • 72934 - Sincerus Florida
    • 72934-8022 - Benzoyl Peroxide 8% / Niacinamide 4%

NDC 72934-8022-6

Package Description: 120 g in 1 BOTTLE, PLASTIC

NDC Product Information

Benzoyl Peroxide 8% / Niacinamide 4% with NDC 72934-8022 is a a human prescription drug product labeled by Sincerus Florida. The generic name of Benzoyl Peroxide 8% / Niacinamide 4% is benzoyl peroxide 8% / niacinamide 4%. The product's dosage form is suspension and is administered via topical form.

Labeler Name: Sincerus Florida

Dosage Form: Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.

Product Type: Human Prescription Drug 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.

Benzoyl Peroxide 8% / Niacinamide 4% Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BENZOYL PEROXIDE 8 g/100g
  • NIACINAMIDE 4 g/100g

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Sincerus Florida
Labeler Code: 72934
Marketing Category: UNAPPROVED DRUG OTHER - 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.

Start Marketing Date: 05-11-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

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Benzoyl Peroxide 8% / Niacinamide 4% Product Label Images

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