Dentalclean Advanced Pro

Dentalclean Advanced Pro is an FDA-registered drug product whose active ingredient is SODIUM FLUORIDE 0.24%. It is labelled by Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 84035-013, application M021, label effective 20260904. 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 cavities, helps prevent, harmful effects, plaque associated, gingivitis builds, increasing protection, against painful, teeth cold. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use • Aids in the prevention of cavities • Helps prevent gingivitis •Helps interfere with harmful effects of plaque associated with gingivitis • Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact.

Directions Adults and children 12 years of age and older: apply at least a 1 inch strip of the product onto a soft bristled toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth. Do not swallow. Children under 12 year of age: consult a dentist.

WARNINGS: When using this product for sensitivity , do not use longer than 4 weeks unless recommended by a dentist. Stop use and ask a dentist if the sensitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. Keep out of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Stop use and ask a dentist if • gingivitis, bleeding, or redness persists for more than 2 weeks • you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs of periodontitis, a serious form of gum disease.

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.

What is Dentalclean Advanced Pro used for?
Use • Aids in the prevention of cavities • Helps prevent gingivitis •Helps interfere with harmful effects of plaque associated with gingivitis • Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact.

Who makes Dentalclean Advanced Pro?
Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda is the labeler of record for Dentalclean Advanced Pro. 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 Dentalclean Advanced Pro 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 Dentalclean Advanced Pro 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 Dentalclean Advanced Pro 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.