MakeSense PHARMA — Class II drug recall D-0483-2017
Terminated recall by Cherry Hill Sales Co., reported 2017-03-01, distributed in FL, IL, MI, NY, PA. CGMP Deviations
| Recall number | D-0483-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cherry Hill Sales Co., Chesapeake, VA, United States |
| Recall initiated | 2017-01-27 |
| Classified | 2017-02-18 |
| Reported by FDA | 2017-03-01 |
| Terminated | 2017-04-19 |
| Distributed | FL, IL, MI, NY, PA |
| Quantity | 3,600 cartons |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00857181005108 |
| NDC | 69020-0205-28 |
| Lot numbers | 04/18, 09/17, 103811, 105304 |
Product
MakeSense PHARMA, HEMORRHOIDAL RELIEF CREAM Phenylephrine HCL-0.25% Zinc Oxide-12.50%,1 oz. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-205-28
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-0483-2017. 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.