Alpha-Pro SODIUM FLUORIDE AND HYDROFLUORIC ACID DENTAL TECHNOLOGIES, INC. FDA Approved Active Ingredients: 1.23% w/w Fluoride Ion (0.79% from Sodium Fluoride and 0.44% from Hydrogen Fluoirde) in 0.1 Molar Phosphoric Acid. DENTAL TECHNOLOGIES LINCOLNWOOD, ILLINOIS 60712 USA www.dentaltech.com Questions or Comments? Call: 1-800-835-0885 (US) or 1-847-677-5500 PM-5097 Rev002
FunFoxMeds bottle
Substance Hydrofluoric Acid
Route
DENTAL
Package NDC

Drug Facts

Composition & Profile

Quantities
68 count
Treats Conditions
Indications And Usage Topical Application Of Apf Gel Is Indicated In The Prevention Of Dental Caries This Treatment Is Normally Used Two Times Per Year And Should Not Exceed Four Times A Year

Identifiers & Packaging

Container Type BOTTLE
All Product Codes
UNII
RGL5YE86CZ 8ZYQ1474W7
Packaging

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.; Principal Display Panel DENTAL TECHNOLOGIES www.dentaltech.com ALPHA-PRO® APF TOPICAL GEL 60 SECOND TREATMENT Acidulated Phosphate Fluoride 1.23% Fluoride Ion Rx Only Strawberry REF No. 009-4201-002 NET WEIGHT: 17.5 oz. (497g) APF_Strawberry

Package Descriptions
  • 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.
  • Principal Display Panel DENTAL TECHNOLOGIES www.dentaltech.com ALPHA-PRO® APF TOPICAL GEL 60 SECOND TREATMENT Acidulated Phosphate Fluoride 1.23% Fluoride Ion Rx Only Strawberry REF No. 009-4201-002 NET WEIGHT: 17.5 oz. (497g) APF_Strawberry

Overview

Active Ingredients: 1.23% w/w Fluoride Ion (0.79% from Sodium Fluoride and 0.44% from Hydrogen Fluoirde) in 0.1 Molar Phosphoric Acid. DENTAL TECHNOLOGIES LINCOLNWOOD, ILLINOIS 60712 USA www.dentaltech.com Questions or Comments? Call: 1-800-835-0885 (US) or 1-847-677-5500 PM-5097 Rev002

Indications & Usage

: Topical application of APF gel is indicated in the prevention of dental caries. This treatment is normally used two times per year and should not exceed four times a year.

Dosage & 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.

Warnings & Precautions
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. Contains FD&C Red No. 40.
Contraindications

: Hypersensitivity to fluoride.

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, urticaria, gastric distress, headache, and weakness.


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