Blume Sunburst Sunscreen

Blume Sunburst Sunscreen is an FDA-registered drug product whose active ingredient is ZINC OXIDE. It is labelled by Blume taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83656-2106, application M020, label effective 20260521. It is one of 404 FDA drug label records sharing the active ingredient ZINC OXIDE. 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 ZINC OXIDE are most often described in connection with: blume sunburst, sunscreen indications. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Blume Sunburst Sunscreen Indications & usage

Blume Sunburst Sunscreen Dosage and Administration

Blume Sunburst Sunscreen Warning Label

FDA lists 404 drug label records with ZINC OXIDE 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 Blume Sunburst Sunscreen used for?
Blume Sunburst Sunscreen Indications & usage

Who makes Blume Sunburst Sunscreen?
Blume is the labeler of record for Blume Sunburst Sunscreen. 404 FDA label records share the active ingredient ZINC OXIDE, 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 Blume Sunburst Sunscreen 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 Blume Sunburst Sunscreen 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 ZINC OXIDE?
Yes. 404 FDA drug label records list ZINC OXIDE 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 Blume Sunburst Sunscreen 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.