CLASS II Drug recall · Reported 10 Oct 2018 · FDA Enforcement Report

Nystatin and Triamcinolone Acetonide Cream, USP/gm & 1 mg/gm recalled

Dr. Reddy's Laboratories is recalling Nystatin and Triamcinolone Acetonide Cream, USP/gm & 1 mg/gm, distributed nationwide in the US. The recall was initiated on 21 Sep 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: a) D06017, D06018, Exp 9/18; D06028 Exp 10/18; b) D06014, D06015, D06016, Exp 9/18; D06024, D06025, D06026, D06027, Exp 10/2018; c) D06011, D06012, D06013, Exp 9/18; D06020, D06021, D06022, D06023, Exp 10/2018
Quantity recalled35020 tubes

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-0007-2019
FDA event ID
81083
Recalling firm
Dr. Reddy's Laboratories, Princeton, NJ
Classification
Class II
Status
Terminated
Recall initiated
21 Sep 2018
FDA classified
4 Oct 2018
Reported
10 Oct 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

21 Sep 2018Recall initiated by company
4 Oct 2018Classified by FDA+13 days
10 Oct 2018Published in enforcement report+6 days

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

Reason for recall

Failed stability specifications - An out of specification result was observed for the test parameter : composition of Nystatin during stability testing.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Nystatin and Triamcinolone Acetonide Cream, USP, 100,000 units/gm & 1 mg/gm, packaged in a) 15 g tube (NDC 43598-431-44), b) 30 g tube (NDC 43598-431-30), c) 60 g tube (NDC 43598-431-60), Rx only, Distributor: Dr. Reddy's Laboratories, Inc. 107 College Road East, Princeton, NJ - 08540 Rx Only Made in India

Where it was distributed

U.S.A. Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Failed stability specifications - An out of specification result was observed for the test parameter : composition of Nystatin during stability testing.

Which lots are affected?

Lot #: a) D06017, D06018, Exp 9/18; D06028 Exp 10/18; b) D06014, D06015, D06016, Exp 9/18; D06024, D06025, D06026, D06027, Exp 10/2018; c) D06011, D06012, D06013, Exp 9/18; D06020, D06021, D06022, D06023, Exp 10/2018

Where was it sold?

U.S.A. Nationwide

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.

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