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Crest

Procter & Gamble Manufacturing Company

Crest Sensi-Relief™


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 lake, yellow 10 lake, iron oxides, blue 1, yellow 5

Questions?

1-800-492-7378

Dist. by Procter & Gamble, Cincinnati, OH 45202

PRINCIPAL DISPLAY PANEL - 116 g Tube Carton

SAME CLINICALLY PROVEN ACTIVE INGREDIENT AS SENSODYNE™

Crest ®

SENSI • RELIEF™

NET WT 4.1 OZ (116 g)
TOOTHPASTE FOR SENSITIVE TEETH AND CAVITY PREVENTION

MAXIMUM STRENGTH*
SENSITIVITY RELIEF

WHITENING

Crest

Crest

Sodium Fluoride and Potassium Nitrate PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-850
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
ALUMINUM OXIDE
D&C YELLOW NO. 10
ferric oxide red
FD&C YELLOW NO. 5

Product Characteristics

Color
GREEN (with dark green gel)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 116 in 1 TUBE
2 24 in 1 TUBE
3 NDC:37000-850-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part356 2013-11-13


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Be sure to consult your doctor before taking any medication!
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