CLASS II Drug recall · Reported 13 Apr 2022 · FDA Enforcement Report

The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint recalled

Revive Personal Products is recalling The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, distributed nationwide in the US. The recall was initiated on 21 Mar 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 3640A, Exp 12/22
Quantity recalled6156 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0751-2022
FDA event ID
89873
Recalling firm
Revive Personal Products, Allendale, NJ
Classification
Class II
Status
Terminated
Recall initiated
21 Mar 2022
FDA classified
6 Apr 2022
Reported
13 Apr 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

21 Mar 2022Recall initiated by company
6 Apr 2022Classified by FDA+16 days
13 Apr 2022Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint, 16.9 FL OZ (500 mL, Manufactured for Revive Personal Products Company, Madison, NJ 07940, UPC Code 714132000714.

Where it was distributed

Nationwide USA

Nationwide

Questions about this recall

Is The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint recalled?

Yes. Revive Personal Products recalled The Natural Dentist Healthy Breath Antiseptic Rinse, Cool Mint on 21 Mar 2022. The recall is Class II and its status is Terminated. Recall number D-0751-2022.

Why was it recalled?

Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states active ingredient as Peppermint Oil and Sage Oil and has the wrong UPC

Which lots are affected?

Lot #: 3640A, Exp 12/22

Where was it sold?

Nationwide USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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