Among fungal pathogens, infections by drug-resistant species continue to pose a major challenge to healthcare. This study aimed to evaluate the activity of the bioactive natural product, penta--galloyl-β-d-glucose (PGG) against multidrug-resistant (MDR) , MDR , and other MDR non- species. Here, we show that PGG has a minimum inhibitory concentration (MIC) of 0.25-8 μg mL (0.265-8.5 μM) against three clinical strains of and a MIC of 0.25-4 μg mL (0.265-4.25 μM) against a panel of other MDR species. Our cytotoxicity studies found that PGG was well tolerated by human kidney, liver, and epithelial cells with an IC > 256 μg mL (>272 μM). We also show that PGG is a high-capacity iron chelator and that deletion of key iron homeostasis genes in rendered strains hypersensitive to PGG. In conclusion, PGG displayed potent anti- activity with minimal cytotoxicity for human cells. We also found that the antifungal activity of PGG is mediated through an iron-chelating mechanism, suggesting that the compound could prove useful as a topical treatment for superficial infections.