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Up and Up Sensitive Toothpaste Whitening

Medically reviewed on Aug 27, 2018

Dosage form: paste
Ingredients: POTASSIUM NITRATE 5mg in 1g, SODIUM FLUORIDE 2.43mg in 1g
Labeler: Team Technologies, Inc
NDC Code: 67659-079

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

UP AND UP SENSITIVE TOOTHPASTE WHITENING

Active IngredientsPotassium nitrate 5%...........................................Antihypersensitivity
Sodium Fluoride 0.243% (0.15% w/v fluoride ion)....Anticavity toothpaste

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

WARNINGS: when using this product do not use longer than 4 weeks unless recommended by a dentist or doctor. Stop and ask a dentist if problems persists or worsens. Sensitive teeth may indicate a serious problem that may require prompt care by a dentist. Keep out of reach of children. If you accidentally swallow more that used for brushing seek professional help or contact a Poison Control Center immediately.

Directions

Adults and children 12 years and older     Brush teeth for at least one minute, preferably after each meal, or at least twice a day or as directed by your dentist. Be sure to brush sensitive areas.

Children under 12 years of age Consult a dentist or doctor

Other information Store in a cool, dry place.

Inactive ingredients:

Sorbitol, Silica, Water, Sodium Lauryl Sulphate, Flavor, Cellulose Gum,Titanium Dioxide, Sodium Benzoate, Sodium Phosphate, Tetrasodium Pyrophosphate, Sodium Saccharin

Principal Display Panel

Antihypersensitivity, Anticavity toothpaste

KEEP OUT OF REACH OF CHILDREN
UP AND UP SENSITIVE TOOTHPASTE WHITENING  
potassium nitrate and sodium fluoride paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67659-079
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM NITRATE (POTASSIUM CATION) POTASSIUM NITRATE5 mg  in 1 g
SODIUM FLUORIDE (FLUORIDE ION ) SODIUM FLUORIDE 2.43 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL 
SILICON DIOXIDE  
WATER 
SODIUM LAURYL SULFATE  
CROSCARMELLOSE SODIUM  
TITANIUM DIOXIDE  
SODIUM BENZOATE  
SODIUM PHOSPHATE  
SODIUM PYROPHOSPHATE  
SACCHARIN SODIUM  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorMINT (Mint Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:67659-079-021 TUBE (TUBE) in 1 CARTON
1NDC:67659-079-01113 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35608/25/2010
Labeler - Team Technologies, Inc (192339703)

 
Team Technologies, Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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