TITANIUM DIOXIDE AND ZINC OXIDE

N/A

Manufactured by KAS Direct LLC dba BabyGanics

69 FDA adverse event reports analyzed

Last updated: 2026-04-15

About TITANIUM DIOXIDE AND ZINC OXIDE

TITANIUM DIOXIDE AND ZINC OXIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by KAS Direct LLC dba BabyGanics. The most commonly reported adverse reactions for TITANIUM DIOXIDE AND ZINC OXIDE include POSTURE ABNORMAL, SEIZURE LIKE PHENOMENA, BLISTER, EYE MOVEMENT DISORDER, APPLICATION SITE RASH. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TITANIUM DIOXIDE AND ZINC OXIDE.

Top Adverse Reactions

POSTURE ABNORMAL4 reports
SEIZURE LIKE PHENOMENA4 reports
BLISTER3 reports
EYE MOVEMENT DISORDER3 reports
APPLICATION SITE RASH2 reports
DERMATITIS CONTACT2 reports
EXTRAPYRAMIDAL DISORDER2 reports
FEELING ABNORMAL2 reports
HYPERSENSITIVITY2 reports
PETIT MAL EPILEPSY2 reports
PRURITUS2 reports
URTICARIA2 reports
ACUTE MYELOID LEUKAEMIA1 reports
ADMINISTRATION SITE RASH1 reports
ADMINISTRATION SITE SWELLING1 reports
APPLICATION SITE BURN1 reports
APPLICATION SITE DRYNESS1 reports
APPLICATION SITE ERYTHEMA1 reports
APPLICATION SITE SWELLING1 reports
ASTHMA1 reports
BALANCE DISORDER1 reports
BURNS SECOND DEGREE1 reports
CHILLS1 reports
COMPLETED SUICIDE1 reports
CRYING1 reports
DEPRESSED LEVEL OF CONSCIOUSNESS1 reports
DEVICE DISLOCATION1 reports
DRUG INEFFECTIVE1 reports
DRY SKIN1 reports
ERYTHEMA1 reports
EXPOSURE TO TOXIC AGENT1 reports
FACIAL PAIN1 reports
GLASSY EYES1 reports
HERPES ZOSTER1 reports
HYPERAESTHESIA1 reports
INTENTIONAL PRODUCT USE ISSUE1 reports
MYOCARDIAL INFARCTION1 reports
PAIN1 reports
PAPULE1 reports
PRODUCT CONTAMINATION CHEMICAL1 reports
PRODUCT LABEL ISSUE1 reports
RASH1 reports
RESPIRATORY DISTRESS1 reports
SCAB1 reports
SCAR1 reports
SEIZURE1 reports
SKIN SWELLING1 reports
SUNBURN1 reports
SWELLING1 reports
SWELLING FACE1 reports
WOUND1 reports

Report Outcomes

Out of 22 classified reports for TITANIUM DIOXIDE AND ZINC OXIDE:

Serious 90.9%Non-Serious 9.1%

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

Female14 (63.6%)
Male5 (22.7%)
Unknown3 (13.6%)

Reports by Age

Age 103 reports
Age 62 reports
Age 41 reports
Age 51 reports
Age 71 reports
Age 81 reports
Age 121 reports
Age 301 reports
Age 611 reports
Age 631 reports
Age 661 reports
Age 671 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 AND ZINC OXIDE?

This profile reflects 69 FDA FAERS reports that mention TITANIUM DIOXIDE AND 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 AND ZINC OXIDE?

Frequently reported terms in FAERS include POSTURE ABNORMAL, SEIZURE LIKE PHENOMENA, BLISTER, EYE MOVEMENT DISORDER, APPLICATION SITE RASH, DERMATITIS CONTACT. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures TITANIUM DIOXIDE AND ZINC OXIDE?

Labeling and FAERS entries often list KAS Direct LLC dba BabyGanics in connection with TITANIUM DIOXIDE AND 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.