Stone Hand Sanitizer

Stone Hand Sanitizer is an FDA-registered drug product whose active ingredient is ISOPROPYL ALCOHOL. It is labelled by handetizer, LLC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85782-018, application 505G(a)(3), label effective 20260826. It is one of 128 FDA drug label records sharing the active ingredient ISOPROPYL 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.

Use Section Use Section

Dosage and Administration Section Directions Section

Warnings Warning Section 1 Warning Section 2

FDA lists 128 drug label records with ISOPROPYL 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.

What is Stone Hand Sanitizer used for?
Use Section Use Section

Who makes Stone Hand Sanitizer?
handetizer, LLC. is the labeler of record for Stone Hand Sanitizer. 128 FDA label records share the active ingredient ISOPROPYL 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 Stone Hand Sanitizer 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 Stone Hand Sanitizer 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 ISOPROPYL ALCOHOL?
Yes. 128 FDA drug label records list ISOPROPYL 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 Stone Hand Sanitizer 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.