Proactiv 10% Bpo Wash Gel
NDC Package 11410-220-01

11-digit billing NDC: 11410022001
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Proactiv 10% Bpo Wash (benzoyl peroxide) gel is sensitivity Test for a New User . Apply product sparingly to one or two small affected areas during the first 3 days. This formulation utilizes a gel delivery system. Marketed by Alchemee, Llc, this product is identified by NDC 11410-220 and is authorized under FDA application M006.

Identification & Billing

NDC Package Code
11410-220-01
Package Description
1 BOTTLE in 1 CARTON / 240 mL in 1 BOTTLE
Product Code
11410-220
11-Digit Billing Format
11410022001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Proactiv 10% Bpo Wash
Non-Proprietary Name
Benzoyl Peroxide
Substance Name
Benzoyl Peroxide
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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 10 g/100mL
Usage Information
Sensitivity 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. cover the entire affected area with a thin layer and rinse thoroughlyone to three times daily. because 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 doctor.if bothersome dryness or peeling occurs, reduce application to once a day or every other day.if 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
Alchemee, Llc
Product Type
Human Otc Drug
FDA Application #
M006
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-12-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 11410-220-01 identifies a specific commercial package of 1 bottle in 1 carton / 240 ml in 1 bottle of Proactiv 10% Bpo Wash, a human over the counter drug labeled by Alchemee, Llc. This gel 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 Alchemee, Llc on August 12, 2026. The current certification is valid through December 31, 2027.

How is this Alchemee, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11410022001. 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 (5-3-2)
11410-220-01
11-Digit CMS (5-4-2)
11410-0220-01

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