Hand San

Hand San is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Rochester Midland Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 59503-2605, application M004, label effective 20260514. It is one of 582 FDA drug label records sharing the active ingredient ALCOHOL. 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 ALCOHOL are most often described in connection with: drug facts, box otc-indications, usage section, hand-washing decrease, skin only. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Drug Facts Box OTC-Indications and Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Dosage & Administration Section Wet hands thoroughly with product and allow to dry without wiping

Drug Facts Box OTC-Warnings Section Flammable, keep away from fire and flames For external use only

FDA lists 582 drug label records with ALCOHOL 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 Hand San used for?
Drug Facts Box OTC-Indications and Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available

Who makes Hand San?
Rochester Midland Corporation is the labeler of record for Hand San. 582 FDA label records share the active ingredient ALCOHOL, 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 Hand San 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 Hand San 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 ALCOHOL?
Yes. 582 FDA drug label records list ALCOHOL 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 Hand San 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.