LICEOUT — Class II drug recall D-0073-2025
Ongoing recall by Neogen Corporation, reported 2024-12-04. CGMP violations.
| Recall number | D-0073-2025 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Neogen Corporation, Lexington, KY, United States |
| Recall initiated | 2024-10-08 |
| Classified | 2024-11-27 |
| Reported by FDA | 2024-12-04 |
| Quantity | 5,328 sachets |
| Reason classes | cgmp |
| NDC | 53427-0124-01 |
| Lot numbers | LO09530 |
| Expiration dates | 2025-09-05 |
Product
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 1 FL. OZ. (29.6 mL) per sachet, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53427-124-01
Reason for recall
CGMP violations.
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-0073-2025. 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.