RedRock Pharmacy
St. George, Utah
1240 East 100 South, Suite 220, St. George, UT 84790
435-703-2900Your prescription should come with a name, clear instructions and a way to ask questions. Start with the pharmacy on your label.

Medically reviewed by Linda West-Conforti, RN · CA RN #389453 ·
A pharmacy name is a starting point for verification. It does not establish which product that pharmacy fills, its current license status in every state, or testing of your specific lot.
Network list last confirmed: July 2026. Confirm the assigned pharmacy for your current prescription with your care team.
Public business details checked September 16, 2026. Use the official lookup for current licensing; this date is not a new confirmation of network assignments.
St. George, Utah
1240 East 100 South, Suite 220, St. George, UT 84790
435-703-2900Florence, Kentucky
7107 Industrial Road, Florence, KY 41042
800-748-7001Bellmore, New York
2657 Merrick Road, Bellmore, NY 11710
516-833-6262Daphne, Alabama
26258 Pollard Road, Daphne, AL 36526
251-380-7630Match the exact name and location on your label. Red Rock and Precision have multiple locations; a business’s general contact page is not proof of the location assigned to your order.
An FDA close-out letter dated May 3, 2023 acknowledges that Triad Rx no longer produced sterile drug products at that time and that the cited warning-letter violations appeared addressed. This historical record does not establish its present capabilities. We do not assign injectable products to Triad based on this directory.
Read the FDA close-out letterUse your prescription label and the official records together.
Use the exact legal name and address from your label in the state board’s public lookup. Check status, expiration, location and any disciplinary record. Also check authorization in the state where you receive medication. An NPI identifies an organization; it is not a pharmacy license or quality certification.
Confirm your name, preparation, concentration, prescribed dose, directions, lot number and beyond-use date. Ask the pharmacist to explain anything unclear before use.
Follow storage instructions for your particular preparation. FDA advises not using injectable GLP-1 medicine that arrives warm or inadequately refrigerated. Contact the pharmacy and care team about damage, temperature concerns or unclear instructions.
They are different federal compounding frameworks with different requirements. Section 503A generally concerns patient-specific compounding; section 503B concerns registered outsourcing facilities. Neither makes a compounded drug FDA-approved. Ask which framework applies to your preparation.
A state license establishes a regulatory registration; an NPI is an identifier. Platform certification addresses the platform. None is FDA approval or proof of a compounded preparation’s clinical results.
Check REMEVi’s LegitScript listing · FDA: compounding questions
Is compounded GLP-1 legal in 2026? What 503A allows →
The network list last confirmed in July 2026 names RedRock Pharmacy, Health Warehouse, Precision Medicine and Triad Rx. A listing does not mean every pharmacy prepares every product. Ask your care team which pharmacy is assigned to your prescription, and confirm the name and address on your label.
Assignment can depend on state authorization, the prescribed preparation and availability. Confirm your assigned pharmacy with the care team. This directory does not promise a specific pharmacy for any product or state.
Use the exact legal name and address from your label in the state board’s public lookup. Check status, expiration, location and any disciplinary record. Also check authorization in the state where you receive medication. An NPI identifies an organization; it is not a pharmacy license or quality certification.
They are different federal compounding frameworks with different requirements. Section 503A generally concerns patient-specific compounding; section 503B concerns registered outsourcing facilities. Neither makes a compounded drug FDA-approved. Ask which framework applies to your preparation.
No. Compounded preparations are not FDA-approved medicines or approved generics. Clinical trial results for the manufacturers’ medicines do not establish the safety or effectiveness of a compounded preparation.
The payment term and shipment schedule are different. Multi-month injectable plans include shipments every four weeks; prepaying does not extend a vial’s usable life. Follow the pharmacy’s storage and beyond-use instructions. FDA recommends discarding compounded multidose GLP-1 vials within 28 days after first use, even if a compounder gives a longer period; follow any shorter limit.
Ask the dispensing pharmacy what testing applies to your preparation and whether documentation is available for your lot. A network listing does not verify potency, sterility, endotoxin testing or a particular accreditation.
Yes. Confirm the pharmacy assigned to your current order. Public contact details can be checked independently, but they do not confirm REMEVi’s current dispensing arrangements.
Your dispensing pharmacist can answer preparation and storage questions. Your REMEVi care team can help you identify the pharmacy assigned to your order.
Contact the care team