Keystone Industries recalls 10 oz. Perio Maintenance Rinse (0.63% Stannous Fluoride) due to subpotent drug content. This Rx-only rinse may not deliver intended dental benefits. Consumers should contact the manufacturer for details.
Subpotent Drug
Keystone Industries is recalling a prescription dental rinse product because it contains less active ingredient than labeled. This means it may not effectively treat gum disease as intended. The recall affects people using this rinse for dental care.
The rinse has a subpotent drug level, meaning it contains less active ingredient than labeled. This could result in the product being less effective for gum disease treatment. However, it does not pose a direct health risk like injury or poisoning.
Prescription dental patients using the recalled Perio Maintenance Rinse. Those with specific dental conditions requiring this rinse are most at risk.
Look for the product name 'Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution' with a mint flavor. Check the label for NDC 68400-202-10 and lot numbers PVC-003015 (expires Sep 2025) or PVC-003061 (expires Apr 2026).
Look for the NDC code 68400-202-10 and lot numbers PVC-003015 or PVC-003061 on the bottle.
The product is safe for use but may not be as effective as intended due to subpotent drug content.
Check the label for NDC 68400-202-10 and lot numbers PVC-003015 (expires Sep 2025) or PVC-003061 (expires Apr 2026).
The recall does not specify a remedy, so contact Keystone Industries directly for guidance.
We’ve drafted a message you can send Keystone Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0046-2025 — Keystone Industries Keystone Industries Hello, I own a Keystone Industries that is covered by recall D-0046-2025 from Keystone Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
