ARG Laboratories recalls ALOE GATOR SPF 40+ sunscreen due to out of specification active ingredients. Consumers should check product labels for the listed ingredients and lot numbers.
Out of Specification for active ingredient
ARG Laboratories is recalling ALOE GATOR SPF 40+ sunscreen because it contains active ingredients at levels outside the required specifications. This could affect the product's effectiveness and safety.
The sunscreen contains active ingredients (Octocrylene, Octyl Methoxycinnamate, Benzophone, Octyl Salicylate) at concentrations that do not meet the required specifications. This could lead to reduced effectiveness or potential safety issues.
People who own or use ALOE GATOR SPF 40+ sunscreen with the specified ingredients and lot numbers are affected. Those with sensitive skin or who rely on sunscreen for protection may be at higher risk.
Check the product label for the ingredients: Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%. The lot number is 04023C1 and expires January 31, 2025.
Look for the ingredients and lot number on the label to confirm if the product is recalled.
The recall is due to out of specification active ingredients, which may affect effectiveness and safety. The official notice does not specify if it is safe to use.
Check the product label for the ingredients: Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%, and lot number 04023C1 (expires 01/31/2025).
The recall record does not specify a remedy, so the official notice does not provide action steps beyond checking the label.
We’ve drafted a message you can send ARG Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0530-2024 — ARG Laboratories ARG Laboratories Hello, I own a ARG Laboratories that is covered by recall D-0530-2024 from ARG Laboratories. 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.
