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Church & Dwight Co., Inc.

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients        
Potassium nitrate 5.0%
Sodium fluoride 0.243%

Purpose

Purpose

Uses

Use 

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

      

Warnings
When using this product
do not use longer than 4 weeks unless recommended by a dentist or physician.

Stop use and ask a dentist if the problem persists or worsens.  Sensitive teeth may indicate a serious problem that may need prompt care by a dentist.

Keep out of 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.

Directions    do not swallow   

adults and children 12 years and older

  • apply at least a 1-inch strip of the product onto a soft bristly toothbrush. Brush teeth for at least one minute, preferable after each meal or at least twice a day (morning and evening) or as recommended by a dentist or physician.  Make sure to brush all sensitive areas of the teeth.

children under 12 years

  • consult a dentist or physician

Inactive ingredients   sodium bicarbonate (baking soda), water, sorbitol, glycerin, hydrated silica, flavor, sodium saccharin, sodium lauroyl sarcosinate, sodium lauryl sulfate, cellulose gum, titanium dioxide, xanthan gum

Questions or comments?  Call 1-800-786-513 5 Monday-Friday 9am-5pm ET or visit www.myoralcare.com

Principal Display Panel


ARM AND HAMMER The Standard of Purity
Fluoride Anti-Cavity Toothpaste     Frosted Mint Flavor

Sensitive                  From the Makers of
                                      Orajel

                Maximum Relief Without a Prescription

NET WT.                                               
4.5 OZ. (127g)           Whitening          with Baking Soda                 

Carton imageSensitive

Sensitive

Sodium Fluoride PASTE, DENTIFRICE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10237-660
Route of Administration DENTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE FLUORIDE ION 2.43 mg
POTASSIUM NITRATE NITRATE ION 50 mg

Inactive Ingredients

Ingredient Name Strength
SODIUM BICARBONATE
water
sorbitol
GLYCERIN
HYDRATED SILICA
SACCHARIN SODIUM DIHYDRATE
SODIUM LAURYL SULFATE
SODIUM LAUROYL SARCOSINATE
CARBOXYMETHYLCELLULOSE SODIUM
titanium dioxide
XANTHAN GUM

Product Characteristics

Color
white

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 127 in 1 TUBE
2 25 in 1 TUBE
3 NDC:10237-660-09 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part355 2012-01-29


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Be sure to consult your doctor before taking any medication!
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