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OTC products · Product label record

Freshmint Premium Anticavity drug information

SODIUM FLUORIDE
New World Imports, Inc · DENTAL

Product NDC: 51824-034

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSODIUM FLUORIDE
Labeler / manufacturerNew World Imports, Inc
RouteDENTAL
Drug classDrug class not supplied in source label
Product NDC51824-034
Label effective date2026-09-08

Official product label reference

Freshmint Premium Anticavity — New World Imports, Inc

This page contains 7 source sections for SODIUM FLUORIDE, dental route. Label set 1a42cf2d-6c48-4e38-97bc-b6f2084bf39b, version 8.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses Aids in the prevention of dental cavities

Purpose

OTC Purpose Anticavity
Dosage and administration — label text
Directions Adults and children 2 years & older: Brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist. Do not swallow. Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing, use a pea-sized amount) Supervise children's brushing until good habits are established. Children under 2 years: Consult a dentist or doctor
Warnings
Warnings Keep out of reach of children under 6 years of age. if you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.
Active ingredient
OTC Active Ingredient Sodium Fluoride - 0.243% (0.15 w/v fluoride ion)
Child safety
Keep out of reach of Children under 6 years of age If you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.
Inactive ingredient
Inactive Ingredients Sorbitol, Silica, Treated Water, Glycerin, PEG-32, Sodium Lauryl Sulfate, Flavor, Titanium Dioxide, Cellulose Gum, Carrageenan, Trisodium Phosphate, Sodium Saccharin, Sodium Benzoate, Tetrasodium Pyrophosphate, FD&C Blue #1

Official sources and product identifiers

Substances listed: SODIUM FLUORIDE

RxNorm identifiers: 891775

Package NDC codes

51824-034-01, 51824-034-09

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.