Touch Acne Treatment Benzoyl Peroxide

Touch Acne Treatment Benzoyl Peroxide is an FDA-registered drug product whose active ingredient is BENZOYL PEROXIDE. It is labelled by Diractions Capital LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73246-001, application M006, label effective 20260710. 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: treatment acne. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the treatment of acne

Directions Clean the skin thoroughly before applying this product Cover the entire affected area with a thin layer 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. Other sun protection measures include limiting sun exposure and wearing protective clothing.

Warnings For external use only Do not use if you Have very sensitive skin Are sensitive to benzoyl peroxide 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 the 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 erduced by using the product less frequently or in a lower concentartion. If going outside, apply sunscreen after using this product. If sensitivity develops or irritation becomes severe, stop use and ask a doctor Keep out of reach of children If swallowed get medical help or call a poison control center immediately Keep away from excessive heat or heat sources

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.

What is Touch Acne Treatment Benzoyl Peroxide used for?
Uses For the treatment of acne

Who makes Touch Acne Treatment Benzoyl Peroxide?
Diractions Capital LLC is the labeler of record for Touch Acne Treatment Benzoyl Peroxide. 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 Touch Acne Treatment Benzoyl Peroxide 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 Touch Acne Treatment Benzoyl Peroxide 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 Touch Acne Treatment Benzoyl Peroxide been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

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.