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Manufactured by Bausch Health US, LLC
8 FDA adverse event reports analyzed
Last updated: 2026-04-15
ZINC OXIDE SUNSCREEN is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Bausch Health US, LLC. The most commonly reported adverse reactions for ZINC OXIDE SUNSCREEN include DRUG INEFFECTIVE, DRY SKIN, ERYTHEMA, PRURITUS, SKIN DISCOMFORT. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ZINC OXIDE SUNSCREEN.
Out of 1 classified reports for ZINC OXIDE SUNSCREEN:
The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.
This profile reflects 8 FDA FAERS reports that mention ZINC OXIDE SUNSCREEN. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include DRUG INEFFECTIVE, DRY SKIN, ERYTHEMA, PRURITUS, SKIN DISCOMFORT, SKIN EXFOLIATION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list Bausch Health US, LLC in connection with ZINC OXIDE SUNSCREEN. Always verify the specific product and NDC with your pharmacist.