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Semaglutide is a synthetic formulation prepared with a focus on quality, consistency, and verified formulation standards. It is manufactured and handled under controlled processes to support dependable purity and composition.
| Component | Description |
|---|---|
| Active Ingredient | Semaglutide (synthetic formulation) |
| Net Content | 5 mg per vial |
| Form | Lyophilized powder |
| Excipients | None added unless otherwise specified |
| Quality Verification | Identity and purity independently confirmed using validated analytical methods such as HPLC or mass spectrometry |
Semaglutide is a well-characterized synthetic formulation with documented structural properties. Any references to published materials are provided for general informational context only and do not constitute usage, dosage, or application guidance.
This product is intended for research purposes only. It is designated strictly for in vitro testing and laboratory experimentation and is not approved for human or animal consumption. All information provided on this website is for educational and informational purposes only. This product should be handled only by licensed and qualified professionals. It is not a drug, food, or cosmetic, and must not be misbranded, misused, or mislabeled as such.
Semaglutide 5 mg is a GLP-1 receptorārelated formulation prepared with a focus on purity, consistency, and verified quality standards. Its molecular profile is manufactured and handled under controlled processes to support dependable formulation integrity.
Each unit is prepared to maintain stability, consistency, and reliable composition across batches.
Semaglutide features a well-defined molecular structure designed to support consistent formulation characteristics and verified quality parameters. Each batch is prepared and managed under strict quality control systems to ensure dependable specifications.
GLP-1 pathwayārelated molecular structure
Verified formulation consistency
Independently tested for purity and composition
Controlled manufacturing and handling standards
Transparent documentation available
Name: Semaglutide
Net Content: 5 mg per vial
Form: Lyophilized powder
Quality Verification: Identity and purity independently verified using validated analytical methods
Storage: Store under recommended cold-storage conditions to maintain integrity
Each vial is prepared to support accurate measurement and consistent handling.
All batches undergo independent analytical verification to confirm identity, purity, and composition prior to availability. Supporting documentation is maintained to ensure transparency and quality assurance.
This offering is not intended to diagnose, treat, cure, or prevent any disease.
No medical, therapeutic, or physiological claims are made or implied.
Purchasers are responsible for ensuring appropriate handling, storage, and compliance with applicable regulations.
Semaglutide is a synthetic formulation prepared with a focus on quality, consistency, and verified formulation standards. It is manufactured and handled under controlled processes to support dependable purity and composition.
| Component | Description |
|---|---|
| Active Ingredient | Semaglutide (synthetic formulation) |
| Net Content | 5 mg per vial |
| Form | Lyophilized powder |
| Excipients | None added unless otherwise specified |
| Quality Verification | Identity and purity independently confirmed using validated analytical methods such as HPLC or mass spectrometry |
Semaglutide is a well-characterized synthetic formulation with documented structural properties. Any references to published materials are provided for general informational context only and do not constitute usage, dosage, or application guidance.
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