Ear Itch MD Anti-Itch Spray — Class II drug recall D-1500-2020
Terminated recall by Eosera, Inc., reported 2020-08-19, distributed nationwide. cGMP Deviations.
| Recall number | D-1500-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Eosera, Inc., Fort Worth, TX, United States |
| Recall initiated | 2020-08-04 |
| Classified | 2020-08-13 |
| Reported by FDA | 2020-08-19 |
| Terminated | 2021-09-10 |
| Distributed | Nationwide (US) |
| Quantity | 43,424 bottles |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00851722007125 |
| NDC | 72429-0071-05 |
| Lot numbers | F193024AUG, F193025, F193026, F193027, F193028, F193029, F193030, F193032, F193054DEC, F193058, F193061JAN, F193069FEB, F193082MAR, F193093APR, F193094MAY, F193095, F203059OCT, F203071SEP |
Product
Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5, UPC 851722007125
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-1500-2020. 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.