Church & Dwight Co Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & recall — FDA D-0790-2026
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
Overview of recall records associated with Church & Dwight Co., Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.
This page summarizes recall records in which the official source identifies Church & Dwight Co., Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.