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Listerine Total Care Fresh Mint Anticavity drug information

SODIUM FLUORIDE
Kenvue Brands LLC · ORAL

Product NDC: 69968-0178

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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 / manufacturerKenvue Brands LLC
RouteORAL
Drug classDrug class not supplied in source label
Product NDC69968-0178
Label effective date2026-08-28

Official product label reference

Listerine Total Care Fresh Mint Anticavity — Kenvue Brands LLC

This page contains 10 source sections for SODIUM FLUORIDE, oral route. Label set b2ce66c3-dc48-47a5-a731-5550bc194679, 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

Use aids in the prevention of dental cavities

Purpose

Purpose Anticavity
Dosage and administration — label text
Directions Adults and children 6 years of age and older: use twice daily after brushing your teeth with a toothpaste vigorously swish 10mL (2 teaspoonfuls) 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 supervise children as necessary until capable of using without supervision Children under 6 years of age: consult a dentist or doctor
Warnings
Warnings Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away .
Unclassified section
Drug Facts Dist: Johnson & Johnson Healthcare Products Division of McNEIL-PPC, Inc. Skillman, NJ 08558-9418
Active ingredient
Active ingredient Sodium fluoride 0.02% (0.01% w/v fluoride ion)
Child safety
Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away .
Storage and handling
Other information store at room temperature cold weather may temporarily cloud this product
Inactive ingredient
Inactive ingredients Water, Alcohol (21.6% v/v), Sorbitol, Poloxamer 407, Eucalyptol, Flavor, Methyl Salicylate, Menthol, Phosphoric Acid, Sodium Saccharin, Thymol, Disodium Phosphate, Sucralose, Red 40, Blue 1
Questions
Questions? Call toll-free 888-222-0182 or 215-273-8755 (collect)

Official sources and product identifiers

Substances listed: SODIUM FLUORIDE

RxNorm identifiers: 313029, 1798474

Package NDC codes

69968-0178-3, 69968-0178-1, 69968-0178-2, 69968-0178-4, 69968-0178-5, 69968-0178-6

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.