Haleon US Holdings LLC parodontax Active GUM Health, Mouthwash, Mint recall: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
The hazard: Drug safety concern
This is an FDA enforcement action. The summary above is the agency’s own description of what went wrong.
What the notice says: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.
Recall details
- Recall number
- D-0297-2026
- Published
- February 4, 2026
- Risk level
- Class III
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Haleon US Holdings LLC
- Product type
- Prescription & OTC drugs
- Units affected
- 84,764 bottles
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot #: 0665363, Exp 08/31/2027. Lot number and Exp Date may not appear on the 500 mL bottle.
Products covered by this recall
parodontax (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
Check your product
The notice names 8 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- 0665363
- Exp 08
- 31
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 08
- 31
NDC number
On the carton and again on the bottle or blister label.
- 0135-0651-02
Package size
Match the net weight or the piece count on the front of the pack.
- 16.9 FL OZ
- 500 mL
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Drug safety
Haleon US Holdings LLC — This is an FDA enforcement action. The summary above is the agency’s own description of what went wrong.
- Check the lot number on your pack against the codes listed above.
- Keep the carton; the lot number is often printed only on the outer pack.
- Report side effects you think the product caused to FDA MedWatch.
- Do not stop a prescribed medicine on your own — speak to your prescriber or pharmacist first.
Refunds and replacements
With medicines, a replacement supply matters more than cash, and that is what pharmacies are set up to provide.
- Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.
- For a mail-order or online pharmacy, use the recall line listed on this page rather than the general support queue.
- If the recall voided a fill you had already paid for, your insurer will normally authorise a replacement ahead of schedule. Quote the recall number.
- If you paid out of pocket, ask for a refund of the co-pay or purchase price and keep the receipt the pharmacy issues.
Company contact: Haleon US Holdings LLC — 184 Liberty Corner Rd Ste 200, Warren, NJ, 07059-6870
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was Haleon US Holdings LLC prescription & otc drugs recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles. Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 0665363, Exp 08, 31; best-by date 08 or 31. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Check the lot number on your pack against the codes listed above.
Can I get my money back?
Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.
Where was the recalled product sold?
It was distributed nationwide.
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