DOCTORS CHOICE description, usages, side effects, indications, overdosage, supplying and lots more!

DOCTORS CHOICE

Massco Dental A Division of Dunagin Pharmaceuticals
Massco Dental A Division of Dunagin Pharmaceuticals

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT


Active Ingredient: Stannous Fluoride

INACTIVE INGREDIENTS

Glycerine, Hydroxy Ethyl Celluulose, Natural Flavor, Xylitol

USE

Aids in the prevention of dental decay.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS FOR USE

Adults and Children 12 years and Older: Use after regular brushing and flossing.  Place gel across length of toothbrush.  Brush Thoroughly.  Keep on teeth for 1 - 1 1/2 minutes and then expectorate (spit out).  Do not swallow.  Use once a day for cavity prevention.  Supervise children until capable of using without supervision.

Children 6-11 Years:  See directions above.  Adult supervision required.

Children Under 6: Consult a Dentist or Physician.

OTHER INFORMATION

This is a fluoride prevention treatment gel, not a toothpaste.  Read directions carefully before use.  This product may produce surface discoloration of the teeth.  Adequate toothbrushing may prevent discoloration.  Discoloration is not harmful or permanent and may be removed by a dental professional.  Do not freeze or expose to extreme heat.

QUESTIONS ? COMMENTS ?

Questions?? Comments??

Call 1-479-787-5168 M-F 9am to 5pm CST

WARNINGS

If more than amount used for brushing is accidentally swallowed, seek medical help from a poison control center.

PACKAGE LABEL

Brush on Therapy for Cavity Prevention - Doctor's Choice 0.4% Stannous Fluoride Gel

Manufactured by Massco Dental


PACKAGE LABEL


PACKAGE LABEL


PACKAGE LABEL

PACKAGE LABEL

DOCTORS CHOICE

STANOUS FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-011
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
stannous fluoride Fluoride Ion .45103 g

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
Xylitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-011-04 120 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 1989-01-01


DOCTORS CHOICE

STANNOUS FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-012
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
stannous fluoride Fluoride Ion .4510 g

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
Xylitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-012-04 120 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 1989-01-01


DOCTORS CHOICE

STANNOUS FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-013
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
stannous fluoride Fluoride Ion .4510 g

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
Xylitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-013-04 120 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 1989-01-01


DOCTORS CHOICE

STANNOUS FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-016
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
stannous fluoride Fluoride Ion .4510 g

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
Xylitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-016-04 120 in 1 BOTTLE, DISPENSING

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 1989-01-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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