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Class III · Lower riskActive recall

Parodontax

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot #: 0665363, Exp 08/31/2027. Lot number and Exp Date may not appear on the 500 mL bottle.
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byHaleon US Holdings LLC
Brand namePARODONTAX
Generic nameCETYLPYRIDINIUM CHLORIDE
Active ingredient(s)CETYLPYRIDINIUM CHLORIDE
Distributed by / forHaleon, Warren, NJ 07059
NDC0135-0651-02
Show the full FDA record
Full product labelparodontax (cetylpyridinium chloride)ACTIVE GUM HEALTH, Mouthwash, Mint. Net Wt 16.9 FL OZ (500 mL), Distributed by Haleon, Warren, NJ 07059. NDC 0135-0651-02
Recalling firmHaleon US Holdings LLC
DistributionNationwide in the USA
Quantity84,764 bottles
Recall initiated2025-12-26
Report date2026-02-04
Recall completed—
Recall numberD-0297-2026
ClassificationClass III
FDA statusOngoing
Origin on fileWarren NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.