PREOP

PREOP is an FDA-registered drug product whose active ingredient is HYDROGEN PEROXIDE. It is labelled by Everbrands, Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72655-200, application M022, label effective 20260420. It is one of 28 FDA drug label records sharing the active ingredient HYDROGEN 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 HYDROGEN PEROXIDE are most often described in connection with: dental procedural, rinsing help, prevent infection, minor oral. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses for dental procedural rinsing to help prevent infection in minor oral irritations

Directions: • Adults and children 2 years of age and older: rinse two pumps (4-5 mL) around in the mouth over the affected area for at least 15 seconds, then spit out • Children under 12 years of age should be supervised in the use of this product • Children under 2 years of age: consult a dentist or physician

Warnings Do not use this product for more than 7 days unless directed by a dentist or physician.

FDA lists 28 drug label records with HYDROGEN 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.

5 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 PREOP used for?
Uses for dental procedural rinsing to help prevent infection in minor oral irritations

Who makes PREOP?
Everbrands, Inc. is the labeler of record for PREOP. 28 FDA label records share the active ingredient HYDROGEN 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 PREOP come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is PREOP 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 HYDROGEN PEROXIDE?
Yes. 28 FDA drug label records list HYDROGEN 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 PREOP been recalled?
5 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.