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Topical 60 Sec Sodium Fluoride Strawberry Package Insert

Status:
Prescription (Rx) Facts
Strength:
123 mg/g
Brand names:
Active ingredient:
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Prescribing information (package insert) - Topical 60 Sec Sodium Fluoride Strawberry

INDICATIONS AND USAGE

For topical application to aid in the prevention of dental caries.

Treatment frequency should not exceed 4 treatments per year.

DOSAGE AND ADMINISTRATION

Shake can thoroughly for at least 10 seconds before each use.

Hold can completely upside down to dispense. Point can toward applicator tray and slowly press nozzle to fill tray. Dry tooth surface and insert tray(s) into mouth. Have patient bite down for 1 minute or up to 4 minutes.

Remove tray(s) and have patient expectorate excess. Instruct patient not to eat, drink, or rinse for 30 minutes.

DOSAGE FORMS AND STRENGTHS

This topical foam contains 1.23% fluoride ion.

CONTRAINDICATIONS

Do not use if patient has a known allergy to fluoride or any of the other ingredients in this product.

WARNINGS AND PRECAUTIONS

  • Do not swallow. Harmful if swallowed.
  • Keep out of reach of children.
  • Contents under pressure. Do not puncture or incinerate can.
  • This product is not intended for home or unsupervised consumer use.
  • Safety and effectiveness below age 3 have not been established.

    There have been no long-term animal studies with this product to evaluate carcinogenic, mutagenic, or impairment of fertility potential.

    Laboratory studies have indicated that repeated use of APF may dull porcelain, composite restorations and sealants.

OVERDOSAGE

If treatment dose is swallowed (less than 100 mg F), administer milk, limewater, or calcium-type antacid. In case of larger doses (1 pint contains 4.5 grams F ion, which is a lethal dose), use ipecac syrup emetic and immediately seek medical help.

Overdose symptoms include nausea, vomiting, diarrhea, and abdominal pain.

ADVERSE REACTIONS

Developing teeth of children under age 6 may become permanently discolored if excessive amounts are repeatedly swallowed. The following adverse reactions are possible in individuals hypersensitive to fluoride: eczema, atopic dermatitis, urticarial, gastric distress, headache, and weakness.

INGREDIENTS

Purified Water, Heptafluoropropane (Propellant), Denatured Ethyl Alcohol (Benzaldehyde), Sodium Fluoride, Crodafos 03A-LQ, Polyethylene Glycol 400, Crodafos MCASA-PA, Cetyl Alcohol, Sodium Methyl Cocoyl Taurate, Sodium Phosphate Monobasic Monohydrate, Artificial Strawberry Flavor, Sodium Saccharin, Sodium Benzoate

STORAGE

Store at 20°C - 25°C (68°F - 77°F); excursions permitted between 15°C - 30°C (59°F - 86°F) [See USP Controlled room temperature.]

Made in U.S.A.

0531150LA, R2-012018

About this document

Source: FDA drug labeling via NLM DailyMed · View the label on DailyMed

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Drug information for Topical 60 Sec Sodium Fluoride Strawberry

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Active ingredient Sodium fluoride 123 mg/g
Dosage form Aerosol, foam
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Patterson Dental Supply Inc
FDA approval UNAPPROVED DRUG OTHERUnapproved drug
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
123 mg/g – 125 g in 1 canister / 1 in 1 box NDC 50227-0501-6

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.