Gonasi 5000 IU
$80.00
Iron Ascension Gonasi 5000 IU (Human Chorionic Gonadotropin / hCG) is a high-purity polypeptide hormone engineered to maintain testicular function, preserve fertility, and accelerate Leydig cell reactivation. Mimicking Luteinizing Hormone (LH), it prevents testicular atrophy during heavy anabolic protocols and lays the essential foundation for full HPTA recovery. Each kit includes dedicated bacteriostatic water for multi-dose reconstitutions.
Guaranteed safe checkout
Description
Description
Iron Ascension Gonasi 5000 IU
Specifications & Composition
| Specification | Details |
|---|---|
| Active Compound | Human Chorionic Gonadotropin (hCG) |
| Concentration | 5,000 IU per vial |
| Total Quantity | 10 mL bacteriostatic water (listed separately as diluent; confirm supplied quantity and packaging) |
| Delivery System | Subcutaneous or intramuscular injection, as prescribed |
| Formulation Standard | Pharmaceutical-grade lyophilized powder (manufacturer claim; verification required) |
| Batch Testing | High-Performance Liquid Chromatography (HPLC) (manufacturer-reported method; confirm suitability for the product) |
Key Performance Features
- LH Receptor Activity: hCG acts on luteinizing hormone (LH) receptors in the testes, stimulating Leydig cells and supporting testosterone production.
- Testicular Function: In selected medical settings, hCG may be used to support testicular steroid production and fertility-related treatment. It should not be described as guaranteed prevention of testicular atrophy during suppressive anabolic steroid use.
- Hormonal Treatment Context: hCG has established medical uses in specific reproductive and endocrine conditions. Claims that it reliably accelerates post-cycle recovery or prepares the body for subsequent SERM treatment are not established guarantees. Treatment requires individualized medical assessment.
Important Health Considerations: hCG can cause hormonal fluctuations, breast tenderness or enlargement, fluid retention, headaches, and injection-site reactions. It may also affect fertility treatment outcomes and requires appropriate clinical monitoring. Injectable products must be sterile and suitable for injection; an assay result alone cannot establish either.
Quality Control & Lab Verification
The manufacturer reports that each batch undergoes quantitative testing before allocation.
| Quality Control Parameter | Reported Result |
|---|---|
| Compound | Human Chorionic Gonadotropin (lyophilized powder) |
| Assay Result | 99.8% active compound (reported) |
| Testing Method | HPLC (reported; method suitability should be confirmed) |
| Verification Status | PASSED (reported; “PERFORMANCE & SUPPORT” is promotional wording, not a laboratory result) |
Publication note: The 99.8% assay result, HPLC report, pharmaceutical-grade designation, vial potency, diluent identity and quantity, and injectable formulation should be verified against genuine, batch-specific documentation. HPLC assay alone does not establish sterility, endotoxin limits, particulate control, contaminant absence, or suitability for injection. The stated 10 mL of bacteriostatic water should be clearly identified as a separate diluent rather than part of the lyophilized powder vial unless the packaging confirms otherwise.
Specifications
- Short Stroke Gas Piston Gas System (Rifle Length)
- 18.6″ Barrel Length ( Mid-Weight style, non-fluted)
- 1:8 Twist Rate Rifling
Reviews
There are no reviews yet.