Benzoyl Peroxide Liquid
NDC Package 82568-0054-5

11-digit billing NDC: 82568005405
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Benzoyl Peroxide liquids is shake wellSensitivity Test for a New User. This formulation utilizes a liquid delivery system. Marketed by Aarna Usa Inc., this product is identified by NDC 82568-0054 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
82568-0054-5
Package Description
148 mL in 1 BOTTLE
Product Code
82568-0054
11-Digit Billing Format
82568005405

Clinical Specifications

Proprietary Name
Benzoyl Peroxide
Non-Proprietary Name
Benzoyl Peroxide
Substance Name
Benzoyl Peroxide
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
BENZOYL PEROXIDE 50 mg/mL
Usage Information
Shake wellSensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated below.wet area to be cleansedapply acne wash and gently massage area for 1-2 minutesrinse thoroughly and pat drybecause excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other dayif going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor.

Regulatory & Marketing

Labeler Name
Aarna Usa Inc.
Product Type
Human Otc Drug
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-25-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (82568-0054). Click a package code to view its specific billing and regulatory data.

82568-0054-8
237 mL in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 82568-0054-5 identifies a specific commercial package of 148 ml in 1 bottle of Benzoyl Peroxide, a human over the counter drug labeled by Aarna Usa Inc.. This liquid is formulated for topical use and contains benzoyl peroxide as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Aarna Usa Inc. on August 25, 2026. The current certification is valid through December 31, 2027.

How is this Aarna Usa Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82568005405. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
82568-0054-5
11-Digit CMS (5-4-2)
82568-0054-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.