MakeSense PHARMA recalled over manufacturing violations
- Recall date
- January 27, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Cherry Hill Sales Co. recalls MakeSense PHARMA, HEMORRHOIDAL RELIEF CREAM Phenylephrine HCL-0.25% Zinc Oxide-12.50%,1 oz. (28 g) tube, Made in China,…
- Recall number
- D-0483-2017
- FDA classification
- Class II
- Brand / firm
- Cherry Hill Sales Co.
- Sold / distributed
- Michigan, Illinois, New York, Florida, Pennsylvania .
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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