UP AND UP SENSITIVE TOOTHPASTE ENAMEL STRENGTHENING FORMULA PLUS WHITENING- potassium nitrate and sodium fluoride paste

Up and UP Sensitive Toothpaste Enamel Strengthening formula plus whitening by

Drug Labeling and Warnings

Up and UP Sensitive Toothpaste Enamel Strengthening formula plus whitening by is a Otc medication manufactured, distributed, or labeled by Team Technologies, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Potassium nitrate 5%................................Antihypersensitivity
Sodium Fluoride 0.15% w/v fluoride ion ......Anticavity

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

If pain/ sensitivity still persists after 4 weeks of use, please visit your dentist. 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. If you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.

Directions

Adults and children 12 years and older             Brush teeth thoroughly at least 1 minute after each meal or at least twice a day or as directed by your dentist. Be sure to brush sensitive areas of the teeth.

Children under 12 years of age                         Consult a dentist or doctor

Other information                                                Store in a cool, dry place.

Inactive ingredients:

Sorbitol, Water, Silica, Glycerin, PEG-6, COCAMIDOPROPYL BETAINE, Xanthan Gum, Flavor, Sodium Saccharin, Titanium Dioxide, Sodium Hydroxide.

Principal Display Panel

PURPOSE

Antihypersensitivity, Anticavity

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

INGREDIENTS AND APPEARANCE

UP AND UP SENSITIVE TOOTHPASTE ENAMEL STRENGTHENING FORMULA PLUS WHITENING 
potassium nitrate and sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67659-081
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM NITRATE	5 mg  in 1 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	1.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
XANTHAN GUM (UNII: TTV12P4NEE)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT (refreshing mint flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67659-081-02	1 in 1 CARTON
1	NDC: 67659-081-01	113 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	08/25/2010

Labeler - Team Technologies, Inc (192339703)