Face Makeup
FDA adverse event reports for this category.
Top reactions reported
MedDRA Preferred Terms, ranked by frequency in the reports. Shown as percent of all reports for this category. A single report can list multiple reactions, so percentages can sum above 100%.
Outcomes
How the reports resolved, shown as percent of all reports. Outcomes can overlap (one report can have multiple outcomes), so percentages do not sum to 100%.
Top products reported in this category
Specific brand/product names that appear most often in reports for Face Makeup. The FDA dataset uses one free-text field for product identity, so this list mixes brand-only entries (e.g. "Vitamin D") and full product names (e.g. "WEN Cleansing Conditioner").
- Johnsons Powder No Upc 19 reports
- Shower To Shower No Upc 6 reports
- Coty Airspun Face Powder 4 reports
- Revlon Face Powder 4 reports
- Vitamin C 4 reports
- Avon Skin So Soft 3 reports
- Instant Lifting Eye Contour 3 reports
- Sephora Perfection Mist Airbrush Foundation 3 reports
- Synthroid 3 reports
- Allegra 2 reports
- Alprazolam 2 reports
- Asthma Pump 2 reports
- Bare Minerals Original Foundation 2 reports
- Benadryl 2 reports
- Cashmere Bouquet Talcum Powder 2 reports
- Clinique Face Powder 2 reports
- Clinique Loose Face Powder 2 reports
- Coty Air Spun Face Powder 2 reports
- Dr. Scholls Foot Powder 2 reports
- Estee Lauder Blush 2 reports
What to do next
Tools for reporting or tracking adverse events — both for cosmetics and the wider universe of prescription and OTC drugs.
Submit a MoCRA-compliant adverse event report to the FDA for a cosmetic product. Free, no login required.
Open the form →Generate a completed FDA 3500A form for a prescription or over-the-counter drug. The drug AE dataset is far larger (~25M reports) than cosmetics, with richer fields and tools.
Open the form →Weekly alerts when new research papers or preprints surface adverse events for a drug you care about. Covers up to three drugs per account.
Get started →Share this page
About this data
This page summarizes adverse event reports from the FDA's adverse event reporting system for cosmetic products. Reactions are coded in MedDRA. Reports come from consumers, health professionals, and industry. The presence of a report does not establish that the product caused the event - it only reflects what was reported to FDA.
Limitations: The public dataset does not include free-text case narratives, only structured fields.
Data as of June 15, 2026. Source: FDA.