CLASS II Drug recall · Reported 1 Mar 2017 · FDA Enforcement Report

MakeSense Pharma Antifungal Cream Clotrimazole 1% tube recalled

Cherry Hill Sales is recalling MakeSense Pharma Antifungal Cream Clotrimazole 1% tube, distributed in Florida, Illinois, Michigan, New York, Pennsylvania. The recall was initiated on 27 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 103803; Exp. 08/17 NDC 69020-203-35 UPC 857181005023
Quantity recalled2,400 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0487-2017
FDA event ID
76407
Recalling firm
Cherry Hill Sales, Chesapeake, VA
Classification
Class II
Status
Terminated
Recall initiated
27 Jan 2017
FDA classified
18 Feb 2017
Reported
1 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone

Timeline

27 Jan 2017Recall initiated by company
18 Feb 2017Classified by FDA+22 days
1 Mar 2017Published in enforcement report+11 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations

Product as listed by the FDA

MakeSense PHARMA ANTIFUNGAL CREAM Clotrimazole 1%, 1.25 oz. (35 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-203-35

Where it was distributed

Michigan, Illinois, New York, Florida, Pennsylvania .

FloridaIllinoisMichiganNew YorkPennsylvania

Questions about this recall

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot # 103803; Exp. 08/17 NDC 69020-203-35 UPC 857181005023

Where was it sold?

Michigan, Illinois, New York, Florida, Pennsylvania .

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 76407

This product is part of a recall event; the main page for the event is MakeSense Pharma, Hemorrhoidal Relief Cream Phenylephrine recalled.

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