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Crest

Procter & Gamble Manufacturing Company

Crest 3D White Luxe


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
Potassium nitrate 5% Toothpaste for sensitive teeth
Sodium fluoride 0.243% (0.14% w/v fluoride ion) Toothpaste for cavity prevention

Crest Uses

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

Warnings

When using this product do not use longer than four weeks unless recommended by a dentist.

Stop use and ask a dentist if problem lasts or gets worse. Sensitive teeth may indicate a serious problem that may need prompt care.

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

Directions

  • do not swallow
  • 12 yrs. & older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth.
  • do not use in children under 12 yrs.

Inactive ingredients

water, hydrated silica, glycerin, sorbitol, trisodium phosphate, sodium lauryl sulfate, flavor, cellulose gum, alcohol (1.09%), xanthan gum, sodium saccharin, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, polyethylene, titanium dioxide, blue 1

Questions?

1-800-492-7378

Dist. by Procter & Gamble,
Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 116 g Tube Carton

Crest ®
3DWHITE

LUXE®

COMPARE TO
SENSODYNE™*+

DUAL ACTION: SENSITIVITY RELIEF +
POWER OF 3D WHITE

SENSITIVITY

TOOTHPASTE FOR SENSITIVE TEETH
AND CAVITY PREVENTION
ENAMEL SAFE WHITENING

PAMPERING MINT

NET WT 4.1 OZ (116 g)

Crest

Crest

Sodium Fluoride and Potassium Nitrate PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-844
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 1.4 mg
POTASSIUM NITRATE NITRATE ION 50 mg

Inactive Ingredients

Ingredient Name Strength
water
HYDRATED SILICA
GLYCERIN
sorbitol
SODIUM LAURYL SULFATE
CARBOXYMETHYLCELLULOSE SODIUM
ALCOHOL
XANTHAN GUM
saccharin sodium
polysorbate 80
SODIUM BENZOATE
cetylpyridinium chloride
BENZOIC ACID
HIGH DENSITY POLYETHYLENE
titanium dioxide
FD&C BLUE NO. 1

Product Characteristics

Color
TURQUOISE (with white specs)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 116 in 1 TUBE
2 NDC:37000-844-04 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2014-02-04


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Be sure to consult your doctor before taking any medication!
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