CLASS II Drug recall · Reported 15 Mar 2023 · FDA Enforcement Report

Nose Better Gel 75% Camphor, 50% Menthol, 50% Allantoin) recalled

Ecometics is recalling Nose Better Gel 75% Camphor, 50% Menthol, 50% Allantoin), distributed nationwide in the US. The recall was initiated on 24 Feb 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 1E253A, Exp. Date AUG-2024
Quantity recalled37,968 metal tube/folding carton

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-0450-2023
FDA event ID
91719
Recalling firm
Ecometics, Norwalk, CT
Classification
Class II
Status
Terminated
Recall initiated
24 Feb 2023
FDA classified
8 Mar 2023
Reported
15 Mar 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material

Timeline

24 Feb 2023Recall initiated by company
8 Mar 2023Classified by FDA+12 days
15 Mar 2023Published 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

CGMP DEVIATIONS

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Nose Better Gel (0.75% Camphor, 0.50% Menthol, 0.50% Allantoin), packaged in 0.46 oz. (13g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Is Nose Better Gel 75% Camphor, 50% Menthol, 50% Allantoin) recalled?

Yes. Ecometics recalled Nose Better Gel 75% Camphor, 50% Menthol, 50% Allantoin) on 24 Feb 2023. The recall is Class II and its status is Terminated. Recall number D-0450-2023.

Why was it recalled?

CGMP DEVIATIONS

Which lots are affected?

Lot #: 1E253A, Exp. Date AUG-2024

Where was it sold?

Nationwide within the United States

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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