The Recall Desk
ModerateFDA (Drugs)·D-0483-2017·Announced 2017-03-01

Cherry Hill Sales Recalls Hemorrhoidal Cream Due to Manufacturing Deviations

Cherry Hill Sales Co. is voluntarily recalling 3,600 cartons of MakeSense Hemorrhoidal Relief Cream due to CGMP deviations.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically involves a temporary or medically reversible adverse health consequence. The source cites CGMP deviations without reporting specific injuries or illnesses, aligning with a Moderate severity rating for a voluntary precautionary recall.

Plain-English summary

Cherry Hill Sales Co. is voluntarily recalling 3,600 cartons of MakeSense PHARMA Hemorrhoidal Relief Cream. The product is a 1 oz (28 g) tube containing Phenylephrine HCL-0.25% and Zinc Oxide-12.50%. The recall was initiated on January 27, 2017, and was classified as Class II by the FDA.

The reason for the recall is Current Good Manufacturing Practice (CGMP) deviations. The affected lots are #103811 (Exp. 09/17) and #105304 (Exp. 04/18). The product was distributed in Michigan, Illinois, New York, Florida, and Pennsylvania. The recall status is Terminated as of April 19, 2017.

Consumers who have this product should stop using it and contact the recalling firm for instructions. The recall was initiated by the firm and notified via telephone.

The recalled product

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
Manufacturer
Cherry Hill Sales Co.
Category
Drug — Topical OTC
Hazard
Affected units
3,600

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Lot #103811
  • Exp. 09/17 Lot #105304
  • Exp. 04/18 NDC 69020-205-28 UPC 857181005108

Distribution

Distributed in 5 states:

Part of a larger recall action

This product is one of 5 recalled by Cherry Hill Sales Co. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →

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