Multivitamins, Sodium Fluoride 0.25 mg

FDA Drug Profile — Flotrex

Multivitamins, Sodium Fluoride 0.25 mg is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Flotrex. Available dosage form: tablet, chewable.

Drug Details

Generic Name
Multivitamins, Sodium Fluoride 0.25 mg
Brand Names
Flotrex
Application Number
Sponsor
PureTek Corporation
NDC Codes
1
Dosage Forms
TABLET, CHEWABLE
Routes
ORAL
Active Ingredients
SODIUM FLUORIDE, VITAMIN A, ASCORBIC ACID, SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN

Indications and Usage

INDICATIONS AND USAGE This prescription chewable tablet is indicated for the prevention and treatment of vitamin and fluoride deficiencies in patients at high risk for dental caries and inadequate dietary intake of essential vitamins. It is specifically formulated to support normal growth and development, promote bone and dental health, and aid in the maintenance of overall metabolic and immune function.

Warnings

WARNING Keep out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. Caution: Do not eat or drink dairy products within one hour of fluoride administration. Should be chewed. This product, as all chewable tablets, is not recommended for children under age 4 due to risk of choking.