EQUATE GLISTENING MINT- sodium fluoride rinse

Equate Glistening Mint by

Drug Labeling and Warnings

Equate Glistening Mint by is a Otc medication manufactured, distributed, or labeled by Walmart Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Sodium Fluoride

Purpose

Anticavity

Use

• Aids in prevention of dental cavities

Warnings

Warnings

Keep out of reach of children.

If more than used for rinsing is accidently swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and Children 6 years of age and older:

• Use once a day after brushing your teeth with a toothpaste
• Vigorously swish 10 mL of rinse between your teeth for 1 minute and then spit out
• Do not swallow the rinse
• Do not eat or drink for 30 minutes after rinsing
• Instruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing)
• Supervise children as necessary until they are capable of using without supervision

Children under 6 years of age: Consult a dentist or doctor

Other information

• Do not use if printed seal is broken or missing
• Recommended storage temperature 59°F-77°F (15°C-25°C)

Inactive ingredients

Citric Acid, Disodium EDTA, Disodium Phosphate, Flavor, Glycerin, Menthol, PEG-40 Hydrogenated Castor Oil, Sodium Benzoate, Sodium Bicarbonate, Sodium Chlorite, Stevia Leaf Extract, Water, Xylitol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE GLISTENING MINT 
sodium fluoride rinse

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-390
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.005 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
SODIUM CHLORITE (UNII: G538EBV4VF)
STEVIA REBAUDIANA LEAF (UNII: 6TC6NN0876)
XYLITOL (UNII: VCQ006KQ1E)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)
DISODIUM PHOSPHATE (UNII: 22ADO53M6F)
MENTHOL (UNII: L7T10EIP3A)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-390-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M022	10/01/2025

Labeler - Walmart Inc. (051957769)