GUM Cavity Prevention Fluoride Mint

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

Medically reviewed by Drugs.com. Last updated on Mar 24, 2025.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:52376-086
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (FLUORIDE ION)	FLUORIDE ION	0.24 g in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description
1	NDC:52376-086-05	24 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	04/01/2018

Labeler - Sunstar Americas, Inc. (025066358)

Revised: 04/2018

Document Id: 5b106bb0-abc3-4dda-b90c-85bda3ef90bc

Set id: 48236fcc-bb05-4732-888b-a7d9a4b9b4e2

Version: 1

Effective Time: 20180401

Sunstar Americas, Inc.

Further information

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

Medical Disclaimer

GUM Cavity Prevention Fluoride Mint

Further information

See also:

Rybelsus

Zepbound

Ozempic

Wegovy

Victoza

Saxenda

Alli

Methamphetamine

Amphetamine

Phentermine