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Under Section 503A of the Federal Food, Drug, and Cosmetic Act, compounding pharmacies can legally prepare individualized medications for patients with valid prescriptions provided the bulk drug substance they use meets one of three criteria: it appears on the FDA's Category 1 list of approved bulk substances, it has a USP/NF monograph, or it is a component of an FDA-approved drug

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Siciska assessed the level of lytic cell death and eryptosis in vitro caused by the phthalates di-n-butyl phthalate (DBP) and butylbenzyl phthalate (BBP) and their metabolites: mono-n-butyl phthalate (MBP) and monobenzyl phthalate (MBzP)