FLUORITAB CHEWABLE description, usages, side effects, indications, overdosage, supplying and lots more!

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FLUORITAB CHEWABLE

Fluoritab Corporation
Fluoritab Corporation




FULL PRESCRIBING INFORMATION

Active ingredient

CONTAINS: 2.2 MG SODIUM FLUORIDE

EACH TABLET CONTAINS 1 MG FLUORIDE

PPM FLUORIDE IONDAILY DOSAGE

IN DRINKING WATERAGE 6 MO. – 3 YRS.AGE 3-6 YRS.AGE 6-16 YRS.

LESS THAN 0.3 PPM0.25 MG 0.50 MG1 MG

0.3 TO 0.6 PPMNONE 0.25 MG 0.50 MG

OVER 0.6 PPMNONENONENONE




Uses

DIRECTIONS: ONE TABLET PER DAY, CHEWED OR PARTIALLY DISSOLVED IN MOUTH BEFORE SWALLOWING, PREFERABLY AT NIGHT AFTER BRUSHING TEETH.

INACTIVE INGREDIENTS: LACTOSE, FLAVOR, SACCHARIN SODIUM, MAGNESIUM STEARATE

PRECAUTION -RECOMMEND DOSAGE ON CHART BELOW SHOULD NOT BE EXCEEDED AS PROLONGED OVERDOSE MAY RESULT IN DENTAL FLUOROSIS.

FLUORITAB CHEWABLE

FLUORITAB CHEWABLE

SODIUM FLUORIDE TABLET, CHEWABLE

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:0288-2203
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 1 mg

Inactive Ingredients

Ingredient Name Strength
LACTOSE
SACCHARIN SODIUM ANHYDROUS
MAGNESIUM STEARATE

Product Characteristics

Color Size Shape
white 7 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0288-2203-01 100 in 1 BOTTLE
2 NDC:0288-2203-10 1000 in 1 BOTTLE
3 NDC:0288-2203-02 5000 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2011-01-09


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