Does a gummy vitamin formulator handle FDA compliance and labeling?

A qualified gummy vitamin formulator should produce a Supplement Facts panel, a Master Manufacturing Record compliant with 21 CFR Part 111, and flag any structure/function claims requiring a 30-day FDA notification under DSHEA. Confirm this scope of work upfront. Third-party testing for potency and contaminants is a separate cost but is strongly recommended before retail launch.