TITANIUM DIOXIDE, ZINC OXIDE

N/A

Manufactured by Edgewell Personal Care Brands LLC

24 FDA adverse event reports analyzed

Last updated: 2026-04-15

About TITANIUM DIOXIDE, ZINC OXIDE

TITANIUM DIOXIDE, ZINC OXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Edgewell Personal Care Brands LLC. The most commonly reported adverse reactions for TITANIUM DIOXIDE, ZINC OXIDE include SUNBURN, APPLICATION SITE VESICLES, APPLICATION SITE ACNE, APPLICATION SITE ERYTHEMA, APPLICATION SITE EXFOLIATION. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TITANIUM DIOXIDE, ZINC OXIDE.

Top Adverse Reactions

SUNBURN3 reports
APPLICATION SITE VESICLES2 reports
APPLICATION SITE ACNE1 reports
APPLICATION SITE ERYTHEMA1 reports
APPLICATION SITE EXFOLIATION1 reports
APPLICATION SITE HYPERSENSITIVITY1 reports
APPLICATION SITE PAIN1 reports
APPLICATION SITE PRURITUS1 reports
APPLICATION SITE RASH1 reports
APPLICATION SITE SWELLING1 reports
DERMATITIS CONTACT1 reports
DRUG INEFFECTIVE1 reports
EYE IRRITATION1 reports
EYELID CYST1 reports
FEELING HOT1 reports
HYPERHIDROSIS1 reports
JOINT SWELLING1 reports
PAIN1 reports
SKIN EXFOLIATION1 reports
SUPERFICIAL INJURY OF EYE1 reports
SUSPECTED PRODUCT QUALITY ISSUE1 reports

Report Outcomes

Out of 6 classified reports for TITANIUM DIOXIDE, ZINC OXIDE:

Serious 66.7%Non-Serious 33.3%

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 Breakdown

Reports by Sex

Female5 (83.3%)
Male1 (16.7%)

Reports by Age

Age 161 reports
Age 381 reports
Age 391 reports
Age 491 reports
Age 661 reports
Age 721 reports

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with TITANIUM DIOXIDE, ZINC OXIDE?

This profile reflects 24 FDA FAERS reports that mention TITANIUM DIOXIDE, ZINC OXIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for TITANIUM DIOXIDE, ZINC OXIDE?

Frequently reported terms in FAERS include SUNBURN, APPLICATION SITE VESICLES, APPLICATION SITE ACNE, APPLICATION SITE ERYTHEMA, APPLICATION SITE EXFOLIATION, APPLICATION SITE HYPERSENSITIVITY. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures TITANIUM DIOXIDE, ZINC OXIDE?

Labeling and FAERS entries often list Edgewell Personal Care Brands LLC in connection with TITANIUM DIOXIDE, ZINC OXIDE. Always verify the specific product and NDC with your pharmacist.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.