LICEOUT — Class II drug recall D-0074-2025
Ongoing recall by Neogen Corporation, reported 2024-12-04. CGMP violations.
| Recall number | D-0074-2025 |
|---|---|
| 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 | 8,328 jugs |
| Reason classes | cgmp |
| NDC | 53247-0124-02 |
| Lot numbers | LO09530, LO10263, LO106024, LO108624, LO110224, LO11303, LO12153, LO12483, LO13183, LO13412 |
| Expiration dates | 2024-11-03, 2024-12-07, 2025-01-26, 2025-05-10, 2025-08-03, 2025-09-05, 2025-11-14, 2026-03-26, 2026-04-11 |
Product
LICEOUT, Liquid Lice Treatment for Human Use, Contents: 128 FL OZ. (3785.4 mL mL) per jug, Distributed By: Bob Barker Company, Inc., 7925 Purfoy Road, Fuquay-Varina, NC 27526. NDC: 53247-124-02
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-0074-2025. 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.