PURE O2 S

PURE O2 S is an FDA-registered drug product whose active ingredient is CHLORINE DIOXIDE(CLO2). It is labelled by Pure O2 taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 75124-0007, label effective 20200501. 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 CHLORINE DIOXIDE(CLO2) are most often described in connection with: hand sanitizer. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

hand sanitizer

for external use only

■ For external use only. ■ Do not use in eyes. ■ lf swallowed, get medical help promptly. ■ Stop use, ask doctor lf irritation occurs. ■ Keep out of reach of children.

What is PURE O2 S used for?
hand sanitizer

Who makes PURE O2 S?
Pure O2 is the labeler of record for PURE O2 S.

What form does PURE O2 S 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 PURE O2 S 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.

Has PURE O2 S 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.