FRESHEN UP- sodium fluoride, potassium nitrate gel, dentifrice 
MKJ BRANDS LLC

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Freshen-up Extra Strength Extra Whitening Sensitive Toothpaste

Drug Facts

Active ingredient

Sodium fluoride 0.24% (0.15% w/v fluoride ion)

Potassium Nitrate 5%

Purpose

Anticavity

Antihypersensitivity

Use

builds increasing protection against painful sensitivity of teeth to cold, heat, acids, sweets or contact

aids in prevention of dental cavities

Warnings

Stop use and ask a dentist if the problem persists or worsens, snesitive teeth may indicate a serious problem that may need prompt care by dentist. Pain senstivity still persists after 4 weeks of use

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

adults and children 12 years of age and olderapply atleast a 1-inch strip of paste onto a soft bristle toothrush. bursh atleast for 2 minutes preferably after each meal or at least twice a day, or as directed by a dentist or physician. Make sure to brush all sensitve areas of the teeth. minimizi swallowing. Spit out after brushing
children under 12 years and underask a dentist or physician

Inactive ingredients

sorbitol, water, hydrated silica, PEG-32, sodium lauryl sulfate, flavor, tetrasodium pyrophosphate, cellulose gum, xlitol, sodium saccharin,titanium dioxide, benzyl alcohol,Tri sodium phosphate, sodium benzoate

Questions?

1-888-880-1504

Dist. by:
MKJ Brands

PRINCIPAL DISPLAY PANEL

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FRESHEN UP 
sodium fluoride, potassium nitrate gel, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77782-002
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE5 g  in 100 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION24 mg  in 100 g
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SODIUM SACCHARIN (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
PEG-32 (UNII: 1212Z7S33A)  
CELLULOSE GUM (UNII: K679OBS311)  
TETRASODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
XYLITOL (UNII: VCQ006KQ1E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77782-002-13113 g in 1 BOTTLE; Type 0: Not a Combination Product02/10/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02102/10/2025
Labeler - MKJ BRANDS LLC (827648101)

Revised: 6/2025
Document Id: 3763947b-98bb-c1f3-e063-6394a90a89ab
Set id: 2ee626d1-6150-87db-e063-6294a90a64d8
Version: 2
Effective Time: 20250612
 
MKJ BRANDS LLC