Can a med spa in Tennessee offer compounded semaglutide or tirzepatide?

Facility · part of The Practice Perimeter

Short answer
Not directly settled — no cited rule bans compounded GLP-1s; they require any compounded sterile injectable to be prepared in compliance with applicable USP standards, and that duty sits on the supplying pharmacy rather than on the med spa.

Tennessee binds sterile compounding to usp and says so twice. “all sterile products shall be prepared in compliance with applicable usp standards for pharmaceutical compounding”, and separately “any facility that compounds sterile products shall comply with applicable usp standards.” Compounded injectables are sterile products, so USP is the operative standard behind any compounded GLP-1 a Tennessee practice administers.

Tenn. Comp. R. & Regs. 1140-07-.02(1); 1140-07-.04(1) · verified Sep 2, 2026 · regulatory monitoring, not legal advice

Related Tennessee rules

  • ⚠️ read the applicability clause before assuming this reaches your practice. The chapter applies “to all pharmacy practice sites and pharmacists, pharmacy interns, pharmacy technicians and supportive personnel involved in the compounding and dispensing of sterile products.” It governs the pharmacy that supplies a med spa rather than the med spa itself — which is precisely why the diligence question in Tennessee is about the supplier.

    Tenn. Comp. R. & Regs. 1140-07-.01 · verified Sep 2, 2026

  • ⚠️ and the standard is waivable — by the board, not by the practice. “The Board of Pharmacy, upon a showing of good cause and in the best interest of the public health, safety and welfare, may waive the requirements of any applicable portion of usp standards”, and “all waiver requests … shall be submitted in writing”. a supplier claiming an exemption should be able to produce the Board’s written grant of it.

    Tenn. Comp. R. & Regs. 1140-07-.02(2) · verified Sep 2, 2026

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