Little Moon Essentials recalls Dream Cream (Camphor 0.45%, Menthol 5%) in 2oz and 4oz glass jars due to CGMP deviations. No specific remedy stated in the recall notice.
CGMP deviations
Little Moon Essentials is recalling Dream Cream products in 2-ounce and 4-ounce glass jars because of manufacturing quality control issues. This recall does not include a specific action for consumers since the remedy is not stated in the official notice.
The recall is for CGMP (Current Good Manufacturing Practice) deviations, which means the product may not meet safety and quality standards during production. This could lead to potential safety concerns, though the exact risk is not specified in the recall notice.
Owners of Little Moon Essentials Dream Cream in 2oz or 4oz glass jars with the listed UPC codes and lot numbers are affected. People using these products for sleep aid may be at risk due to potential quality issues.
Check for glass jars labeled 'Little Moon Essentials Dream Cream' with 2oz (57g) or 4oz (113g) sizes. Look for the UPC codes 6 73673 88214 5 or 6 73673 88804 8 and specific lot numbers listed in the recall.
Identify if your Dream Cream is in a 2oz or 4oz glass jar with the listed UPC codes and lot numbers.
The recall notice does not state a specific remedy or action for consumers.
The recalled products have specific lot numbers: for 2oz jars, 328260, 321221, 425120, 427230; for 4oz jars, 327150, 326260, 320270, 321301, 422020.
The recall notice does not specify a return or disposal action.
We’ve drafted a message you can send Little Moon Essentials to request your refund or repair — edit it as you like.
Subject: Recall D-0574-2024 — Little Moon Essentials Little Moon Essentials Hello, I own a Little Moon Essentials that is covered by recall D-0574-2024 from Little Moon Essentials. 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.
