CLASS II ONGOING Drug recall · Reported 10 Jul 2024 · FDA Enforcement Report

Dream Cream (Camphor 45%, Menthol 5%), Packaged as a) recalled

Little Moon Essentials is recalling Little Moon Essentials, Dream Cream (Camphor 45%, Menthol 5%), Packaged as a), distributed nationwide in the US. The recall was initiated on 20 Jun 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codeslot code no expiration dates on product: a) 328260, 321221, 425120, 427230, b) 327150, 326260, 320270, 321301, 422020
Quantity recalled1264 glass jars

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-0574-2024
FDA event ID
94788
Recalling firm
Little Moon Essentials, Dania Beach, FL
Classification
Class II
Status
Ongoing
Recall initiated
20 Jun 2024
FDA classified
2 Jul 2024
Reported
10 Jul 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material

Timeline

20 Jun 2024Recall initiated by company
2 Jul 2024Classified by FDA+12 days
10 Jul 2024Published in enforcement report+8 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

Little Moon Essentials, Dream Cream (Camphor 0.45%, Menthol 5%), Packaged as a) 2OZ (57G) glass jar, UPC Code 6 73673 88214 5, NDC 70722-232-02; b) 4OZ (113G) glass jar, UPC Code 6 73673 88804 8, NDC 70722-232-04; Little Moon Essentials LLC Dania Beach, Fl 33004

Where it was distributed

Nationwide USA and Ontario, Canada (2 retailers)

Nationwide

Questions about this recall

Is Dream Cream (Camphor 45%, Menthol 5%), Packaged as a) recalled?

Yes. Little Moon Essentials recalled Dream Cream (Camphor 45%, Menthol 5%), Packaged as a) on 20 Jun 2024. The recall is Class II and its status is Ongoing. Recall number D-0574-2024.

Why was it recalled?

CGMP deviations

Which lots are affected?

lot code no expiration dates on product: a) 328260, 321221, 425120, 427230, b) 327150, 326260, 320270, 321301, 422020

Where was it sold?

Nationwide USA and Ontario, Canada (2 retailers)

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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