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GUM Cavity Prevention Fluoride Mint

Medically reviewed by Drugs.com. Last updated on Mar 22, 2021.

Dosage form: paste, dentifrice
Ingredients: SODIUM FLUORIDE 0.24g in 100g
Labeler: Sunstar Americas, Inc.
NDC Code: 52376-086

GUM Cavity Prevention Fluoride Toothpaste Mint

Drug Facts

Active ingredient

Sodium Fluoride 0.24% (0.14% w/v fluoride ion)

Purpose

Anticavity

Use

helps 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 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 6 years of age

  Instruct in good brushing and rinsing habits (to minimize swallowing).

  Supervise children as necessary until capable of using without supervision.

 Children under 2 years of age

  Consult a dentist or doctor.

Inactive ingredients

Sorbitol, Water, Hydrated Silica, Glycerin, Sodium Lauryl Sulfate, Flavor, Xanthan Gum, Titanium Dioxide, Trisodium Phosphate, Sodium Saccharin, Cellulose Gum, Methylparaben

Questions?

1-800-528-8537 Mon-Fri (7am-6 pm CST)

SUNSTAR

Manufactured by: Sunstar Americas, Inc., 301 E. Central Road, Schaumburg, IL 60195, U.S.A. TBE000013Z

GUMbrand.com

TWIST OFF CAP AND REMOVE SEAL.

DO NOT USE IF SEAL IS NOT INTACT.

Packaging

GUM CAVITY PREVENTION FLUORIDE MINT 
sodium fluoride paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52376-086
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION0.24 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL 
WATER 
HYDRATED SILICA 
GLYCERIN 
SODIUM LAURYL SULFATE 
XANTHAN GUM 
TITANIUM DIOXIDE 
SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS 
SACCHARIN SODIUM 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
METHYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:52376-086-0524 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35504/01/2018
Labeler - Sunstar Americas, Inc. (025066358)

 
Sunstar Americas, Inc.

Further information

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