Ollie Fresh Mint

Ollie Fresh Mint is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE, POTASSIUM NITRATE. It is labelled by Brio Product Group LLC. taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 87493-000, application M022, label effective 20260806. It is one of 4 FDA drug label records sharing the active ingredient SODIUM FLUORIDE, POTASSIUM NITRATE. 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 SODIUM FLUORIDE, POTASSIUM NITRATE are most often described in connection with: helps protect, against cavities. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Helps protect against cavities

Directions • Adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or us as directed by a dentist • Do not swallow • To minimize swallowing use a pea-sized amount in children under 6. • Supervise children’s brushing until good habits • Children under 2 years ask a dentist.

Warnings Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a poison Control Center right away.

FDA lists 4 drug label records with SODIUM FLUORIDE, POTASSIUM NITRATE 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 Ollie Fresh Mint used for?
Uses Helps protect against cavities

Who makes Ollie Fresh Mint?
Brio Product Group LLC. is the labeler of record for Ollie Fresh Mint. 4 FDA label records share the active ingredient SODIUM FLUORIDE, POTASSIUM NITRATE, 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 Ollie Fresh Mint come in?
administered by dental. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Ollie Fresh Mint 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 SODIUM FLUORIDE, POTASSIUM NITRATE?
Yes. 4 FDA drug label records list SODIUM FLUORIDE, POTASSIUM NITRATE 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 Ollie Fresh Mint 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.