Zicam® and Orajel™: Cold Remedy Nasal Swabs, Nasal AllClear Swabs, Baby Teething Swabs — FDA announcement Jun 6, 2025

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Jun 6, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Cold Remedy Nasal Swabs, Nasal AllClear Swabs, Baby Teething Swabs
Reason
Microbial contamination
Classification
Not supplied
Recalling firm
Church & Dwight Co., Inc.
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
e12d904623f33008

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityZicam® Cold Remedy Nasal Swabs, with UPC 732216301205, all lots: A zinc-free, homeopathic cold remedy swab designed to shorten the duration of the common cold.; Zicam® Nasal AllClear Swabs, with UPC 732216301656, all lots: A nasal cleansing swab product (discontinued in December 2024).; Orajel™ Baby Teething Swabs, with UPC 310310400002, all lots: Pre-moistened swabs designed to soothe teething discomfort in infants and toddlers.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

The recalled products were distributed nationwide in the United States and in Puerto Rico.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Fda listing date
Jun 6, 2025
Company announcement date
Jun 6, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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