Menthol Recall: Dr. Bump Natural Pain Relief Gel
Announced 2025-12-03 · FDA
The FDA is recalling 4,890 bottles of Dr. Bump Natural Pain Relief Gel, Menthol 5%, Lot D54947, exp 4/30/2028, due to CGMP deviations. The product was distributed in CA, CO, FL, PR, and WA. Corrective action details were not provided.
| Brand | CA BOTANA International, Inc. |
|---|---|
| Product | Dr. Bump Natural Pain Relief Gel, Menthol 5%, NET WT 4 FL OZ/118 ML per bottle, Distr. by 1Beauty US LLC, Palm Desert, CA 92211. NDC: 35192-052-18, UPC 8 18204 02513 8 |
| Reason | CGMP Deviations |
| Severity | moderate |
| Units affected | 1492 |
| Distribution | CA, CO, FL, PR, WA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using any recalled Dr. Bump Natural Pain Relief Gel from Lot D54947.
- Dispose of the product or return it to the retailer per the distributor’s instructions.
- Check your bottle’s lot number (D54947) and expiry date (4/30/2028) to confirm if it is affected.
- Contact CA BOTANA International, Inc. or 1Beauty US LLC for disposal instructions or more information, or visit the FDA recall page.
How to identify the recalled item
| Lot / date codes | Lot D54947, exp 4/30/2028 |
|---|---|
| Lot / date codes | Lot D54098, exp 3/31/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.