Plak Smacker Anti Cavity Fluoride

Plak Smacker Anti Cavity Fluoride is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE. It is labelled by YOUNG PS ACQUISITION, LLC taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 72326-8002, application M021, label effective 20231016. 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 dental. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use Aids in the prevention of dental cavities.

Directions Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician. Do not swallow To minimize swallowing use a pea sized amount in children under 6 years. Supervise children's brushing until good habits are established. Children under 2 years of age, consult a dentist or physician.

Warnings Keep out of the 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. Do not use if inner foil is torn, cut, or missing. Keep out of reach of children.

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 Plak Smacker Anti Cavity Fluoride used for?
Use Aids in the prevention of dental cavities.

Who makes Plak Smacker Anti Cavity Fluoride?
YOUNG PS ACQUISITION, LLC is the labeler of record for Plak Smacker Anti Cavity Fluoride. 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 Plak Smacker Anti Cavity Fluoride 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 Plak Smacker Anti Cavity Fluoride 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 Plak Smacker Anti Cavity Fluoride 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.