Proactiv 10% BPO Wash

Proactiv 10% BPO Wash is an FDA-registered drug product whose active ingredient is BENZOYL PEROXIDE. It is labelled by Alchemee, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 11410-220, application M006, label effective 20260810. It is one of 56 FDA drug label records sharing the active ingredient BENZOYL PEROXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing BENZOYL PEROXIDE are most often described in connection with: management acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use for the management of acne

Directions 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 thoroughly one 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.

Warnings For external use only When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. avoid unnecessary sun exposure and use a sunscreen. avoid contact with eyes, lips and mouth. avoid contact with hair and dyed fabrics, which may be bleached by this product. skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration. Do not use if you have very sensitive skin are sensitive to benzoyl peroxide Stop use and ask a doctor if irritation becomes severe. If pregnant or breast‑feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 56 drug label records with BENZOYL PEROXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Proactiv 10% BPO Wash used for?
Use for the management of acne

Who makes Proactiv 10% BPO Wash?
Alchemee, LLC is the labeler of record for Proactiv 10% BPO Wash. 56 FDA label records share the active ingredient BENZOYL PEROXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Proactiv 10% BPO Wash come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Proactiv 10% BPO Wash prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing BENZOYL PEROXIDE?
Yes. 56 FDA drug label records list BENZOYL PEROXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Proactiv 10% BPO Wash been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.