DentiCare Pro-Foam description, usages, side effects, indications, overdosage, supplying and lots more!

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DentiCare Pro-Foam

AR Medicom Inc
AR Medicom Inc

DentiCare Pro-Foam 2.72% Topical Sodium Fluoride Foam CinnaMint




FULL PRESCRIBING INFORMATION

Keep out of reach o children. Avoid spraying towards open flame. Store at room temperature. Do not expose to excessive heat over 40C or 104F. Contents under pressure. Do not puncture or incinerate. Do not use if seal is broken.

DentiCare Pro-Foam

Medicom

DentiCare  Pro-Foam

2.72% Topical Sodium Fluoride Foam

CinnaMint

NDC 64778-1372-1

10037-CINM

Purified water, sucralose, sodium phosphate monobasic, xylitol, cocamidopropyl betaine, poloxamer 407, cinnamon flavor, peppermint oil.

Uses

Following prophylaxis treatment, fill 1/4 of tray with foam. To dispense, shake bottle vigorously then invert applicator 180° downward to the bottom of the tray. Insert tray, have patient bite down lightly for a minimun of 60 seconds, up to 4 minutes, remove tray and have patient expectorate excess. Advise patient not to eat, drink or rinse for 30 minutes after the treatment

DentiCare Pro-Foam

Sodium Fluoride AEROSOL, FOAM

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:64778-1372
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 0.0272 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64778-1372-1 125 in 1 BOTTLE, SPRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2003-05-01


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