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Acclean Anti-Cavity Sensitivity Relief

Generic: POTASSIUM NITRATE, SODIUM FLUORIDE

Verified·Apr 23, 2026
Manufacturer
Henry Schein
NDC
0404-0174
RxCUI
637365
Route
TOPICAL
ICD-10 indication
K03.81

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About Acclean Anti-Cavity Sensitivity Relief

What is this medication? Acclean Anti-Cavity Sensitivity Relief is a prescription-strength fluoride treatment used primarily to prevent dental cavities and reduce tooth hypersensitivity. It contains a high concentration of sodium fluoride, which helps to remineralize tooth enamel and protect surfaces from acid erosion and bacterial decay. This medication is often prescribed for individuals who are at a higher risk for developing tooth decay or for those who have weakened enamel that requires more intensive protection than standard over-the-counter toothpastes provide.

The second key component of this medication is potassium nitrate, which is specifically included to alleviate discomfort caused by sensitive teeth. It works by reaching the nerves inside the teeth and blocking the transmission of pain signals triggered by hot, cold, sweet, or acidic stimuli. By combining enamel-strengthening fluoride with a desensitizing agent, this product offers a comprehensive solution for patients who experience chronic tooth pain alongside a need for professional-grade cavity prevention.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Acclean Anti-Cavity Sensitivity Relief. Official source: DailyMed (NLM) · Label effective Nov 14, 2024

Indications and usage
1 INDICATIONS AND USAGE Acclean Prescription Strength Anti-Cavity Toothpaste for Sensitivity Relief is indicated for use as part of a professional program for the prevention and control of dental caries.
Dosage and administration
2 DOSAGE AND ADMINISTRATION Follow these instructions or use as instructed by a dental professional. Adults and children age 12 or older, apply a thin ribbon or pea-sized amount of Acclean Prescription Strength Anti-Cavity Toothpaste for Sensitivity Relief to a toothbrush and brush thoroughly on all tooth surfaces for at least one minute. After use: Adults should expectorate. For best results, do not eat, drink, or rinse for 30 minutes. Children, age 12 to 16, should expectorate after use and rinse mouth thoroughly. Use twice daily as your normal dentifrice or as directed by your dental professional.
Contraindications
4 CONTRAINDICATIONS Do not use in children under 12 years of age unless recommended by a dentist or physician.
Warnings and precautions
5 WARNINGS AND PRECAUTIONS DO NOT SWALLOW. Keep out of reach of children under 12 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Prolonged daily ingestion may result in various degrees of dental fluorosis in children with developing dentition, especially if the water fluoridation exceeds 0.6 ppm, since younger children frequently cannot perform the brushing process without significant swallowing. Use in children under age 6 years requires special supervision to prevent repeated swallowing of toothpaste which could cause dental fluorosis. Read directions carefully before using. Keep out of reach of infants and children. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or physician.
Adverse reactions
6 ADVERSE REACTIONS Allergic reactions and other idiosyncrasies have rarely been reported.
Use in pregnancy
8.1 Pregnancy Pregnancy Category B It has been shown that fluoride crosses the placenta of rats, but only 0.01% of the amount administered is incorporated in fetal tissues. Animal studies (rats, mice, rabbits) have shown that fluoride is not a teratogen. Maternal exposure to 12.2 mg fluoride/kg of body weight (rats) or 13.1 mg/kg of body weight (rabbits) did not affect the litter size or fetal weight and did not increase the frequency of skeletal or visceral malformations. There are no adequate or well controlled clinical studies in pregnant women. However, epidemiological studies conducted in areas with high levels of naturally fluoridated water showed no increase in birth defects. Heavy exposure to fluoride during in utero development may result in skeletal fluorosis which becomes evident in childhood.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.