Revive Personal Products recalls Cool Mint antiseptic rinse due to incorrect labeling and bar code errors. Check for wrong active ingredients listed on back label.
“Revive Natural Dentist Healthy Breath Rinse Recall: Label Mix-Up Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35067-revive-natural-dentist-healthy-breath-rinse-recall-label-mix-up. Based on FDA recall #D-0751-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0751-2022%22&limit=1).
The FDA announced on March 21, 2022, that Revive Personal Products Company is recalling The Natural Dentist Healthy Breath Antiseptic Rinse due to a labeling error. The product's back label incorrectly lists the active ingredient and displays the wrong UPC code.
The recall involves a labeling mix-up where the back label incorrectly states the active ingredient as Peppermint Oil and Sage Oil. It also features the wrong UPC code.
Context
GovInfoNow's records show Revive Personal Products Company has one other recall on record since September 28, 2021. On September 28, 2021, The Natural Dentist issued a mouthwash recall for a label mix-up involving incorrect active ingredients and UPC codes. Other recent recalls of similar products include Beekeeper's Naturals Saline Nasal Spray (June 1, 2026), ORL Kids Natural Toothpaste (December 8, 2025), and Sage Products 2% Chlorhexidine Cloth (August 18, 2026).
How to tell if you have this one
Check for the UPC code 714132000714 and lot number 3640A on the label. The product was manufactured in Madison, NJ and expires December 2022.
Brand
Revive Personal Products
Product
The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, 16.9 FL OZ (500 mL, Manufactured for Revive Personal
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Label Details
Look for the UPC code 714132000714 and lot number 3640A on the back label.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide USA” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #D-0751-2022 (March 21, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0751-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.