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On April 30, 2026, the FDA further proposed formally excluding both from the 503B Bulks List - a proposal that, if finalized after the June 29, 2026 comment period, would close the remaining large-scale outsourcing facility pathway
L., & Bjerre, M
Routine clinical follow-up should be considered if patients experience persistent burning that doesn't resolve quickly after injection, burning that progressively worsens with successive doses, or development of nodules, lumps, or skin changes at injection sites
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