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Published on November 30th, 2025

They are not approved by the FDA for any therapeutic indication and are not intended for human or veterinary consumption

2017, 18.: 10.3390/ijms18122589 Zhang Y-P, Chu R-X, Liu H: Vitamin A intake and risk of melanoma: a meta-analysis

Budovsky A, Yarmolinsky L, Ben-Shabat S

That is, prescribers who work in both LTC and non-LTC settings may still be subject to compliance actions on the basis of Schedule II, III, IV, and V controlled substance prescriptions written for covered Part D drugs for beneficiaries in non-LTC settings if such prescribers do not otherwise qualify for an exception or waiver

The field remains in early stages requiring more research establishing optimal protocols, defining responder characteristics, proving long-term safety, and conducting large randomized trials