Iodent Sensitive Extra Whitening description, usages, side effects, indications, overdosage, supplying and lots more!

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Iodent Sensitive Extra Whitening

UNITED EXCHANGE CORP.




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients                                        Purpose

Potassium nitrate 5%................................. Antihypersensitivity

Sodium fluoride (0.15% w/v fluoride ion)...... Anticavity

Purpose

Uses

  • builds increasing protection against painful sensitivity of the teeth due to cold, heat, acids, sweets or contact
  • aids in the prevention of dental cavities

Warnings

Stope use and ask a dentist if

  • the problem persists or worsens. Sensitive teeth mauy indicate a serious problem that may prompt care by a dentist
  • pain/sensitivity stil persists after 4 weeks of use

Keep out of reach of children. If more than used for brushing is accidently swallowed, get medical help or contact a Poison Control Center right away.

Uses

Directions

  • adults and children 12 years of age and older
  • apply at least a 1-inch strip of product onto a soft bristle toothbrush
  • brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing.
  • children under 12 years of age: consult a dentist or doctor

Other information

  • store belowe 30°C (86°F)
  • Lot No. & Exp Date: see box or see crimp of tube

Inactive ingredients

sorbitol, silica, treated water, polyethylene glycol 1500, sodium lauryl sulphate, glycerin, flavor, sodium carboxy methyl cellulose, tetra sodium pyrophosphate, titanium dioxide, sodium benzoate, tri sodium orth phosphate, sodium saccharin, sodium hydroxide, methyl paraben, propyl paraben

Distributed by:

United Exchange Corp.

17211 Valley View Ave.

Cerritos, CA 90703

Iodent Sensitive Extra Whitening

Iodent Sensitive Extra Whitening

Sodium Fluoride Potassium Nitrate PASTE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65923-105
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 5 mg
POTASSIUM NITRATE NITRATE ION 2.43 mg

Inactive Ingredients

Ingredient Name Strength
sorbitol
HYDRATED SILICA
water
POLYETHYLENE GLYCOL 1500
GLYCERIN
CARBOXYMETHYLCELLULOSE SODIUM
titanium dioxide
SODIUM BENZOATE
saccharin sodium
SODIUM HYDROXIDE
METHYLPARABEN
PROPYLPARABEN

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 113 in 1 TUBE
2 NDC:65923-105-04 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2014-06-12


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