Compounding Pharmacy · Irving, TX · Both

Carie Boyd Pharmaceuticals Review

Carie Boyd Pharmaceuticals is a Texas-based compounding pharmacy operated by Right Value Drug Stores, LLC. The company runs an FDA-registered 503B outsourcing facility at 8400 Esters Blvd, Suite 190, Irving, TX 75063 (registered with FDA as an outsourcing facility on July 3, 2019), plus a 503A patient-specific compounding pharmacy doing business as Carie Boyd's Prescription Shop in Denton, TX (also referenced at 122 Grapevine Hwy, Hurst, TX per NPPES NPI 1205253085, Texas pharmacy license 165). The 503A pharmacy roots trace to a community pharmacy founded in 1965 in the Dallas-Fort Worth area. For GLP-1 weight management, Carie Boyd markets a sublingual semaglutide suspension compounded exclusively with commercially available Rybelsus tablets in a SubMagna sublingual base (starting dose 1 mg/day, titrated to ~1.5 mg/day); no public marketing was found for compounded tirzepatide. The company received an FDA Warning Letter on December 17, 2024 (reference 694687) citing 503B compliance and labeling deficiencies, and a prior Warning Letter on September 20, 2021 (reference 610751) following a 2019 inspection. Both warning letters reduce confidence in this pharmacy for telehealth-provider sourcing relative to peers without active FDA enforcement on file.

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BothFDA-registered 503B outsourcing facility
Location: Irving, TX
States licensed: 0
5.0
★★☆☆2.5/5

Editorial score · methodology

Top-Rated GLP-1 Partners

Not sourced from Carie Boyd Pharmaceuticals — these are our highest-scored vetted telehealth partners for compounded GLP-1s, if you'd rather start with a provider we've walked through end to end.

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No insurance needed · HSA/FSA eligible · vetted by our editors

8.2

Gala

Compounded GLP-1/GIP combo on a yearly plan with free shipping

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6.9

TMates

Nationwide compounded GLP-1 availability including Puerto Rico

Starting price: $249/mo

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7.9

Trimi Health

Budget-conscious shoppers

Starting price: $99/mo

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8.0

ShedRx

Mainstream telehealth GLP-1 access

Starting price: $149/mo

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Certifications & Compliance

All sterile compounding pharmacies in the United States are required to follow United States Pharmacopeia General Chapter <797> sterile compounding standards[4], with finished preparations evaluated against USP <71> sterility testing[5] and USP <85> bacterial endotoxin testing[6] as appropriate for the product type.

FDA-registered 503B outsourcing facility
Registered directly with the FDA as a 503B outsourcing facility. Subject to FDA inspection and required to follow cGMP standards.

Drugs Produced

Compounding pharmacies' ability to produce semaglutide or tirzepatide depends on the FDA Drug Shortage List status for each reference product; compounding eligibility can change when a drug moves on or off the shortage list[7].

Semaglutide
Compounded semaglutide produced
Tirzepatide
Not produced

States Licensed

Carie Boyd Pharmaceuticals has not published a state-by-state licensure list. Verify licensure for your state directly with your state board of pharmacy before filling a prescription here.

Regulatory Actions

2024-12-17
2021-09-20

Weight Loss Rankings Score Breakdown

Accreditation & Compliance6/10
Regulatory Standing5/10
State Coverage0/10
GLP-1 Production5/10
Track Record5/10

Scores are independently researched. See our methodology for details.

Medium confidence · Last verified 2026-05-28 via Eli Marsden · How we verify provider data

Frequently Asked Questions

Carie Boyd Pharmaceuticals is a Both compounding pharmacy based in Irving, TX. It operates under state board of pharmacy licensure. Note: our records show 2 documented regulatory action(s) — see the Regulatory Actions section below.
Carie Boyd Pharmaceuticals is headquartered in Irving, TX. The pharmacy is licensed to ship to 0 US states.
Carie Boyd Pharmaceuticals produces compounded semaglutide in addition to other compounded preparations. As a Both pharmacy, it operates both a patient-specific 503A division and an FDA-registered 503B outsourcing facility.
503A pharmacies prepare compounded medications for individual patients in response to specific prescriptions and are regulated primarily by state boards of pharmacy under USP <797> sterile compounding standards. 503B outsourcing facilities register directly with the FDA, follow current Good Manufacturing Practices (cGMP), and can produce compounded medications in larger batches without patient-specific prescriptions. 503B facilities are subject to FDA inspection.

Key terms, explained

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Sources & methodology — as of August 2026
  1. 1.FDA — Compounding and the 503A Pharmacy FrameworkU.S. Food & Drug Administration.
  2. 2.FDA — 503B Outsourcing Facility Registration and RequirementsU.S. Food & Drug Administration.
  3. 3.PCAB — Pharmacy Compounding Accreditation Board StandardsAccreditation Commission for Health Care (ACHC) / PCAB.
  4. 4.USP General Chapter <797> — Pharmaceutical Compounding: Sterile PreparationsUnited States Pharmacopeia.
  5. 5.USP General Chapter <71> — Sterility TestsUnited States Pharmacopeia.
  6. 6.USP General Chapter <85> — Bacterial Endotoxins TestUnited States Pharmacopeia.
  7. 7.FDA — Drug Shortages Database (current shortage listings)U.S. Food & Drug Administration.