Essentials Whiten and Strengthen

Essentials Whiten and Strengthen is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE 0.24%. It is labelled by Church & Dwight Co., Inc. taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 10237-672, application M021, label effective 20260723. It is one of 3 FDA drug label records sharing the active ingredient SODIUM FLUORIDE 0.24%. 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 0.24% 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 decay

Directions do not swallow supervise children as necessary until capable of using without supervision rinse away toothpaste residue thoroughly after brushing adults and children 2 years and older - brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician children under 6 years - instruct in good brushing and rinsing habits (to minimize swallowing) children under 2 years - ask a dentist or physician

Do not use if irritation occurs and persists

FDA lists 3 drug label records with SODIUM FLUORIDE 0.24% 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.

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Essentials Whiten and Strengthen used for?
Use aids in the prevention of dental decay

Who makes Essentials Whiten and Strengthen?
Church & Dwight Co., Inc. is the labeler of record for Essentials Whiten and Strengthen. 3 FDA label records share the active ingredient SODIUM FLUORIDE 0.24%, 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 Essentials Whiten and Strengthen 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 Essentials Whiten and Strengthen 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 0.24%?
Yes. 3 FDA drug label records list SODIUM FLUORIDE 0.24% 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 Essentials Whiten and Strengthen been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.