One Minute Sodium Fluoride Gel
Generic name: sodium fluoride, phosphoric acid and hydrofluoric acidsodium fluoride, phosphoric acid and hydrofluoric acid
Dosage form: dental gel
Drug class:Mouth and throat products
Medically reviewed by Drugs.com. Last updated on Apr 21, 2022.
Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
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Indications and Usage:
Topical application of APF gel is indicated in the prevention of dental caries.
Warning:
Keep out of reach of children. Do not swallow.
If swallowed during treatment, administer milk, limewater, or antacid. If larger dose is ingested (more than 1/4 ounce), contact poison control and immediately seek medical help.Precautions:
For professional use only. Repeated use may cause dulling of porcelain and ceramic restorations.
Adverse reactions:
Developing teeth of children under age 6 may become permanently discolored if excessive amounts are repeatedly swallowed. Individuals hypersensitive to fluoride may have an adverse reaction.
Dosage and Administration:
After thorough prophylaxis, place gel in applicator tray (not more than 1/3 full). Throughly air-dry teeth and insert tray(s) in mouth. Gel may also be swab applied. Instruct patient to bite down slightly but firmly for one to four minutes. A slight chewing motion enhances coverage interproximally. Remove tray(s) and have patient expectorate excess gel. Instruct patient not to eat, drink or rinse for at least 30 minutes.
How Supplied:
A gel, one bottle contains up to 68 individual applications. Store at controlled room temperature 20°- 25°C (68°-77°F).
Do not allow to freeze.
Active Ingredients:
1.23% w/w Fluoride Ion (0.79% from Sodium Fluoride and 0.44% from Hydrogen Fluoride) in 0.1 Molar Phosphoric Acid
Contains: FDandC Red #40 and FDandC Blue #1
TIME TO REORDER! CALL YOUR DENTAL DEALER.
DISTRIBUTED BY
BIOTROL
Earth City, MO 63045
www.biotrol.com
Questions or Comments?
Call: 1-800-822-8550
12000335 Rev 12/2006
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NDC 0273-7001-16
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