ORTHO GUARD description, usages, side effects, indications, overdosage, supplying and lots more!

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ORTHO GUARD

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


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

ACTIVE INGREDIENT (IN EACH 10 ml) 

SODIUM FLUORIDE 4.4 mg  PURPOSE - ANTICAVITY

INACTIVE INGREDIENTS

INACTIVE INGREDIENTS: DEMINERALIZED WATER, MONOSODIUM PHOSPHATE, SODIUM BENZOATE, SODIUM SACCHARIN, ARTIFICIAL COLORING, ARTIFICIAL FLAVORING

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 6 YEARS AND OLDER

USE ONCE A DAY AFTER BRUSHING YOUR TEETH WITH TOOTHPASTE.  VIGOROUSLY SWISH 10 MILLILITERS (10 ml ON CAP OR 2 TEASPOONS) OF RINSE BETWEEN YOUR TEETH FOR 1 MINUTE THEN SPIT OUT.  DO NOT EAT OR DRINK FOR 30 MINUTES AFTER RINSING.  INSTRUCT CHILDREN UNDER 12 YEARS OF AGE IN GOOD RINSING HABITS TO AVOID SWALLOWING.

CHILDREN UNDER 6

CONSULT A DENTIST OR PHYSICIAN

OTHER INFORMATION

STORE AT ROOM TEMPERATURE

QUESTIONS ? COMMENTS ?

QUESTIONS? COMMENTS?  CALL 1-479-787-5168 M-F 9 am TO 5pm CST

WARNINGS

WHEN USING THIS PRODUCT DO NOT SWALLOW UNLESS TOLD TO DO SO BY A DENTIST OR PHYSICIAN.

IF MORE SOLUTION IS ACCIDENTALLY SWALLOWED THAN USED FOR RINSING, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

PACKAGE LABEL

ORTHOGUARD ANTI-CAVITY FLUORIDE RINSE 0.044% SODIUM FLUORIDE IN AN ACIDULATED PHOSPHATE TOPICAL SOLUTION.  MANUFACTURED BY MASSCO DENTAL A DIVISION OF DUNAGIN PHARMACEUTICALS, GRAVETTE AR (479) 787-5168.  WWW.MASSCODENTAL.NET


ORTHO GUARD


ORTHO GUARD


ORTHO GUARD

ORTHO GUARD

ORTHO GUARD

SODIUM FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-400
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION .044 mL

Inactive Ingredients

Ingredient Name Strength
Sodium Phosphate, Monobasic, Monohydrate
SODIUM BENZOATE
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-400-16 473 in 1 BOTTLE

Marketing Information

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


ORTHO GUARD

SODIUM FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-401
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION .044 mL

Inactive Ingredients

Ingredient Name Strength
water
Sodium Phosphate, Monobasic, Monohydrate
SODIUM BENZOATE
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-401-16 473 in 1 BOTTLE

Marketing Information

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


ORTHO GUARD

SODIUM FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-402
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION .044 mL

Inactive Ingredients

Ingredient Name Strength
water
Sodium Phosphate, Monobasic, Monohydrate
SODIUM BENZOATE
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-402-16 473 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 1998-01-01


ORTHO GUARD

SODIUM FLUORIDE GEL, DENTIFRICE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:63783-403
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION .044 mL

Inactive Ingredients

Ingredient Name Strength
water
Sodium Phosphate, Monobasic, Monohydrate
SODIUM BENZOATE
saccharin sodium

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63783-403-16 473 in 1 BOTTLE

Marketing Information

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


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Be sure to consult your doctor before taking any medication!
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