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DR. Fresh Dailies Travel by Dr. Fresh, Inc.

Dosage form: paste
Ingredients: SODIUM FLUORIDE 0.15g in 100g
Labeler: Dr. Fresh, Inc.
NDC Code: 64893-210

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.

DR. Fresh Dailies Travel Kit

Drug Facts

Active Ingredient

Sodium fluoride 0.243 percent    (0.15 percent w v fluoride ion)        

Purpose

Anticavity Toothpaste

Use:

aids in the prevention of dental cavities

Warnings

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 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.
 Children under the age of 6: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
 Children under 2 years of age: Ask a dentist or doctor

Inactive Ingredients:

Aloe Vera Extract, Carbomer, Fragrance, Glycerin, Isopropyl Myristate, Propylene Glycol, Titanium Dioxide, Triethanolamine, Vitamin E, Water

Questions or Comments

Toll Free: 1-866-DR-Fresh (1-866-373-7374) or comments drfresh.com

Visit us online at: www.drfresh.com

Monday-Friday 8:30 am to 5:30 pm

Package Labeling:

DR. FRESH DAILIES TRAVEL 
sodium fluoride paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64893-210
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION0.15 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
CARBOXYPOLYMETHYLENE 
GLYCERIN 
ISOPROPYL MYRISTATE 
PROPYLENE GLYCOL 
TITANIUM DIOXIDE 
TROLAMINE 
WATER 
Packaging
#Item CodePackage Description
1NDC:64893-210-001 TUBE in 1 KIT
124 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35507/16/2010
Labeler - Dr. Fresh, Inc. (078508990)
Establishment
NameAddressID/FEIOperations
The Procter & Gamble Manufacturing Company007130032manufacture(64893-210)

 
Dr. Fresh, Inc.

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Medically reviewed on Jul 24, 2018

Further information

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

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