Dental plus Whitening description, usages, side effects, indications, overdosage, supplying and lots more!

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Dental plus Whitening

Tropical International Manufacturing Inc


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Sodium Monofluorophosphate 0.8% (1,000 ppmF)

Purpose

anticavity

Use

For cavity prevention, Tooth Protection and Whiter Teeth.

Warnings


Keep out of the reach of children under 6 years of age.

If more than used for brushing is accidentally swallowed, get medical help or contact a poison control center right away.


Drug Facts (continued)

Dental plus Whitening 172g

Directions










Adults and children 2 years of age and older
Children 2 to 6 years

Children under 2 years
Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by dentist or physician.
Use only a pea-sized amount and supervise child brushing and rinsing (to minimize swallowing)
Ask a dentist or a physician

Inactive ingredients

Water, Sorbitol, Calcium Carbonate, Silica, PEG-32, Sodium Lauryl Sulphate, Cellulose Gum, Sodium Bicarbonate, Flavor, Titanium Dioxide, Sodium Saccharin, Sodium Benzoate, Zinc Citrate

Questions? Comments?

call toll-free 1-888-777-8767. Monday-Friday 9am-5pm

Made by Tropical Degil Cosmetics

Ind. Ltd. Kiryat Shmona, Israel for

Tropical International Cosmetics, Inc.

18 Stewart Street,

Brooklyn, NY 11207 USA

Made in Israel

PRINCIPAL DISPLAY PANEL - 6 oz Tube

ANTICAVITY FLUORIDE TOOTHPASTE

Tropical DEGIL Dental plus Whitening

FOR HEALTHY AND BRIGHT TEETH

NET WT.6 OZ (172 G) Cont. Neto: 6 oz (172 G)

Dental plus Whitening

For best results, squeeze tube from

the bottom and flatten as you go up

Dental plus Whitening

SODIUM MONOFLUOROPHOSPHATE PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62678-216
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION 8 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 172 in 1 TUBE
2 NDC:62678-216-16 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2010-05-19


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