FDAClass II · Drug · Recall D-0790-2026 · Recalled September 2, 2026

Zicam recall — Church & Dwight Co., Inc.

Agency report date: September 2, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Zicam
Company / brand: Church & Dwight Co
Lot / serial / date codes: Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028.
Distribution: US Nationwide.

Agency product description and boundaries

Zicam, 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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Zicam recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: D-0790-2026
Brand: All Church & Dwight Co recalls
Classification: Class II
Units affected: 318,600 cartons
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Zicam recall status

Companies & origin

Recalling firm location: Ewing, NJ, United States
Firm address: 500 Charles Ewing Blvd, N/A, 08628-3448

Identifying details (verbatim from the notice)

Product codes / lots: Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028.
Distribution: US Nationwide.
Firm notified the public via: Letter
FDA event ID: 99604
Recall initiated: August 10, 2026
FDA classified: August 26, 2026
FDA report date: September 2, 2026

Other drug recalls from around the same time

Glutathione 200 mg/mL recall — OPTIMAL BALANCE PHARMACYFDA · September 9, 2026
0 recall — Baxter Healthcare CorporationFDA · September 9, 2026
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Tyenne (tocilizumab-aazg) Injection recall — Fresenius Kabi USA, LLCFDA · September 2, 2026
Papaverine HCl Injection recall — American Regent, Inc.FDA · August 26, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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