ALOE GATOR — Class II drug recall D-0523-2024
Ongoing recall by ARG Laboratories, Inc., reported 2024-06-05, distributed nationwide. Out of Specification for active ingredient
| Recall number | D-0523-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARG Laboratories, Inc., Dallas, TX, United States |
| Recall initiated | 2024-04-17 |
| Classified | 2024-05-30 |
| Reported by FDA | 2024-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 4,013 |
| Reason classes | specification failure |
| Lot numbers | 04023C1 |
| Expiration dates | 2025-01-31 |
Product
ALOE GATOR, (Octocrylene 8%, Octyl Methoxycinnamate 6%, Benzophone 3 6%, Octyl Salicylate 5%), Original Formula, SPF 40+, Broad Spectrum Protective Gel, Sport Performance, NET WT 1 OZ (28 g), Manufactured for AGS Brands.
Reason for recall
Out of Specification for active ingredient
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0523-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.