Eye 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 Eye 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").
- Vitamin D 8 reports
- Johnsons Powder No Upc 6 reports
- Synthroid 6 reports
- Calcium 5 reports
- Fish Oil 5 reports
- Levothyroxine 5 reports
- Maybelline Great Lash Mascara 5 reports
- Multivitamin 5 reports
- Vitamin C 5 reports
- Lancome Cils Booster Xl 3 reports
- Magnesium 3 reports
- Mascara 3 reports
- Maybelline Great Lash Mascara (Blackest Black) 3 reports
- Multi Vitamin 3 reports
- Plaquenil 3 reports
- Sertraline 3 reports
- Zinc 3 reports
- Aleve 2 reports
- Allegra 2 reports
- Avon Skin So Soft 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.
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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.