Brand Family

Hydroxycut Products in FDA Data

Individual FDA adverse event report counts for Hydroxycut product variants. Counts are per-product — they are never combined across SKUs.

These are reports submitted to the FDA. A report does not mean any product caused the effect. Each SKU's count is tracked individually and is never summed across variants.

Hydroxycut Product Variants

Each entry is a distinct product as named in FDA reports. Click any product to see its full adverse event breakdown.

Hydroxycut Regular 353 reports · 2009–2014
Hydroxycut 204 reports · 2004–2025
Hydroxycut Hardcore 195 reports · 2008–2025
Hydroxycut Caffeine-free 53 reports · 2009–2012
Hydroxycut Max Liquid Caps 33 reports · 2009–2012
Hydroxycut With Ephedra 28 reports · 2010–2017

Data Source

Data from FDA's CFSAN Adverse Event Reporting System (CAERS). Reports are voluntary submissions — they do not establish that any product caused any event.

View openFDA CAERS source ↗ · About our methodology