N/A
Manufactured by 111MedCo LLC
3 FDA adverse event reports analyzed
Last updated: 2026-04-15
ZINC OXIDE, TITANIUM DIOXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by 111MedCo LLC. The most commonly reported adverse reactions for ZINC OXIDE, TITANIUM DIOXIDE include CONDITION AGGRAVATED, ERYTHEMA, RASH PUSTULAR. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for ZINC OXIDE, TITANIUM DIOXIDE.
Out of 1 classified reports for ZINC OXIDE, TITANIUM DIOXIDE:
The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.
Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.
This profile reflects 3 FDA FAERS reports that mention ZINC OXIDE, TITANIUM DIOXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.
Frequently reported terms in FAERS include CONDITION AGGRAVATED, ERYTHEMA, RASH PUSTULAR. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.
Labeling and FAERS entries often list 111MedCo LLC in connection with ZINC OXIDE, TITANIUM DIOXIDE. Always verify the specific product and NDC with your pharmacist.