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Class II · ModerateActive recall

Zicam

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028.
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Distributed by / forChurch & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205
Show the full FDA record
Full product labelZicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.
Recalling firmChurch & Dwight Co., Inc.
DistributionUS Nationwide.
Quantity318,600 cartons
Recall initiated2026-08-10
Report date2026-09-02
Recall completed—
Recall numberD-0790-2026
ClassificationClass II
FDA statusOngoing
Origin on fileEwing NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.