Day & Night Pack Ear Itch MD Anti-Itch Spray — Class II drug recall D-1501-2020
Terminated recall by Eosera, Inc., reported 2020-08-19, distributed nationwide. cGMP Deviations.
| Recall number | D-1501-2020 |
|---|---|
| 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 | 15,229 bottles |
| Reason classes | cgmp |
| NDC | 72429-0071-05 |
| Lot numbers | TP203006JUN, TP203009, TP203012, TP203055OCT, TP203073SEP |
Product
Day & Night Pack Ear Itch MD Anti-Itch Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles/Ear Itch MD Nighttime Intensive Soothing Spray (pramoxine HCL 1%), 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0071-5
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-1501-2020. 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.