SprinJene Fresh Boost

SprinJene Fresh Boost is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE. It is labelled by Health and Natural Beauty USA Corp taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 63404-0910, application M021, label effective 20260814. It is one of 263 FDA drug label records sharing the active ingredient SODIUM FLUORIDE. 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 are most often described in connection with: prevention caries. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use Helps in the prevention of caries

Directions Supervise children as necessary until capable of using without supervision Adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day as directed by a dentist or physician. Children under 2 to 6 years instruct in good brushing and rinsing habbits (to minimize swallowing). Children under 2 years do not use unless directed by a dentist or physician.

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 263 drug label records with SODIUM FLUORIDE 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 SprinJene Fresh Boost used for?
Use Helps in the prevention of caries

Who makes SprinJene Fresh Boost?
Health and Natural Beauty USA Corp is the labeler of record for SprinJene Fresh Boost. 263 FDA label records share the active ingredient SODIUM FLUORIDE, 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 SprinJene Fresh Boost 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 SprinJene Fresh Boost 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?
Yes. 263 FDA drug label records list SODIUM FLUORIDE 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 SprinJene Fresh Boost 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.