A 60-year-old white woman developed lesions of the conjunctiva and skin consistent with iododerma. Excision and examination of one of the skin lesions and the conjunctival lesion disclosed pseudoepitheliomatous hyperplasia associated with acute and chronic inflammation. The remaining lesions disappeared with cessation of iodide. We review the clinical and histopathologic features of the halodermas and discuss the ocular manifestations of iodide hypersensitivity. Recognition may require exceedingly careful testing, but such care is necessary because fatal cases of iododerma have occurred.