1.Description

Ipamorelin is one of several synthetic met-enkephalin analogs that include unnatural D-amino acids. They were developed for their growth hormone (GH) releasing activity, then called GH secretatogues. They lack opioid activity but are potent stimulators of GH release.

2. Mechanism of Action

Ipamorelin significantly increases plasma growth hormone (GH) levels in humans. In addition, ipamorelin stimulates body weight gain in humans. Like pralmorelin and GHRP-6, ipamorelin does not affect prolactin, follicle-stimulating hormone (FSH), luteinizing hormone (LH), or thyroid-stimulating hormone (TSH) levels. However, unlike pralmorelin (GHRP-2) and GHRP-6, but similarly to growth hormone-releasing hormone (GHRH), ipamorelin does not stimulate the secretion of adrenocorticotropic hormone (ACTH) or cortisol, and is highly selective for inducing the secretion only of GH.

3. Adverse reactions

There have been no reported side effects during the past few years since IPAMORELIN became popular by athletes. After thorough research, there are simply no reports to confirm any side effects.

4. Instructions for reconstitution

Powder must be dissolved only with the solventprovided. 1. Apply the needle to the syringe. Remove the plastic cover from the vial

2. Break the top of the ampoule containing the solvent. Remove the plastic cover of the needle. Make sure the needle is well applied to the syringe. Slowly absorb all the solvent.

3. Inject all the solvent to the vial. This will create a 2mg/ml solution. To prevent foaming, the solvent should be

injected into the vial by aiming the stream of liquid against the glass wall. 4. Following reconstitution, the vial should be swirled with a GENTLE rotary motion until the contents are completely

dissolved. DO NOT SHAKE. The result ing solution should be clear and colorless, without particulate matter.

5. Dosage

• Inject 2ml water into the vial of Ipamorelin from the water vial. 1 full syringe is 1ml. • Once dissolved and clear in colour you draw out 0.1 on the syringe each morning before breakfast, 0.1 each day

before lunch, and 0,1 each day before bed.

• A total of 300 mcg a day, you inject it into the tummy under the skin into the fatty skin layer. • A vial should last 5 days. The doses respectively can be increased after week 1 to 0.15 ie. 450mcg a day.

6. Storage

• This product can be used not more than 3 years from the production date (see box) • After reconstitution, may be stored for a maximum of 14 days in a refrigerator at 2°C-8°C

• Store vials in an upright position.

• Store in a refrigerator (2°C -8°C). Keep in the outer carton in order to protect from light For one month can be stored at room temperature.