Unguentine Original Maximum Strength Pain Relieving/Antiseptic… — Class II drug recall D-0452-2023
Terminated recall by Ecometics, Inc., reported 2023-03-15, distributed nationwide. CGMP DEVIATIONS
| Recall number | D-0452-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ecometics, Inc., Norwalk, CT, United States |
| Recall initiated | 2023-02-24 |
| Classified | 2023-03-08 |
| Reported by FDA | 2023-03-15 |
| Terminated | 2023-06-21 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| Lot numbers | 1E346A, 2E304A, NOV-23, OCT-24 |
Product
Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Oxide 6.6%), packaged in 1 oz. (28.3g) metal tubes, Distributed by: Oakhurst Company Levittown, NY 11756
Reason for recall
CGMP DEVIATIONS
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-0452-2023. 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.