Rock Town Distillery recalls 70% alcohol hand sanitizer due to FDA finding acetal and acetaldehyde levels above specifications. Products with NDC 74492-0002-1 to 4 are affected. No remedy provided in recall notice.
CGMP Deviations: FDA analysis found product to contain acetal and acetaldehyde above specification limits.
Rock Town Distillery is recalling its 70% alcohol hand sanitizer products because FDA testing found acetal and acetaldehyde levels higher than allowed. This could pose a risk of skin irritation or other adverse reactions, though the recall does not specify serious injury.
FDA testing found the hand sanitizer contains acetal and acetaldehyde in amounts exceeding the manufacturer's specifications. These chemicals can cause skin irritation or other adverse reactions in some users, though the risk is not severe enough to cause serious injury.
People who own or use Rock Town Distillery's 70% alcohol hand sanitizer products with NDC codes 74492-0002-1 through 4 are affected. Those with sensitive skin may be at higher risk of irritation.
Check for the NDC codes 74492-0002-1 (375 mL), 74492-0002-2 (3785 mL), 74492-0002-3 (236 mL), or 74492-0002-4 (473 mL) on the product label. Products were made in the USA at Rock Town Distillery in Little Rock, Arkansas.
Look for NDC codes 74492-0002-1 through 4 on the hand sanitizer label.
The recall notice does not provide a remedy, so no action is required beyond checking if you have the affected products.
FDA testing found acetal and acetaldehyde levels above the manufacturer's specifications.
Check for NDC codes 74492-0002-1 (375 mL), 74492-0002-2 (3785 mL), 74492-0002-3 (236 mL), or 74492-0002-4 (473 mL) on the product label.
We’ve drafted a message you can send Rock Town Distillery to request your refund or repair — edit it as you like.
Subject: Recall D-0715-2022 — Rock Town Distillery Rock Town Distillery Hello, I own a Rock Town Distillery that is covered by recall D-0715-2022 from Rock Town Distillery. 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.
