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ANADROL 25 OXYMETHOLONE – 25MG PER TAB

Description for ANADROL 25 OXYMETHOLONE – 25MG PER TAB

Introduction: A Potent Therapeutic Agent from GenLabs

GenLabs Pharmaceuticals presents ANADROL 25, a high-dose formulation of the potent synthetic anabolic-androgenic steroid (AAS) Oxymetholone. Each tablet is precisely dosed at 25mg of pharmaceutical-grade Oxymetholone, packaged in a substantial clinical quantity of 200 tablets. This product is manufactured under strict cGMP (current Good Manufacturing Practice) standards, ensuring consistent potency, purity, and accurate dosage for therapeutic applications where indicated. Oxymetholone, the active compound in ANADROL 25, possesses a unique pharmacological profile, characterized by significant anabolic (tissue-building) and marked erythropoietic (red blood cell-stimulating) properties. It is recognized in clinical endocrinology and hematology as one of the most powerful oral anabolic agents available for medical use.

Primary Clinical Indications and Therapeutic Rationale

ANADROL 25 is not a general supplement; it is a serious medication for specific pathologies. Its primary and most critical use in modern medicine is as a second-line treatment for certain types of anemia that are refractory to other therapies.

  1. Anemia Associated with Bone Marrow Failure: Its most significant application is in the management of aplastic anemia (a condition where the bone marrow fails to produce sufficient blood cells). In cases where patients are not immediate candidates for bone marrow transplantation, Oxymetholone can serve as a hematinic agent to stimulate the bone marrow. It is particularly noted for its ability to increase the production of red blood cells (RBCs), thereby reducing dependency on frequent blood transfusions and improving quality of life.

  2. Constitutional Aplastic Anemia (Fanconi's Anemia): It has a documented history of use in this specific genetic form of aplastic anemia.

  3. Anemia in Myelodysplastic Syndromes (MDS): May be used cautiously in some MDS cases to alleviate anemic symptoms.

  4. Other Catabolic States (Historical/Contextual): In past decades, it was used more broadly for weight gain in catabolic conditions like severe burns, chronic infections, and certain cancers. However, due to its potent side-effect profile, its use for these purposes has been largely superseded by safer, more targeted therapies in most clinical settings.

Crucially, ANADROL 25 is NOT indicated for:

  • Enhancement of athletic performance or physique.

  • Treatment of anemia due to iron, B12, or folate deficiency (it will not help and may mask underlying issues).

  • Use as a general "strength" or "mass-building" supplement.

Pharmacological Profile and Mechanism of Action

Chemical Structure: Oxymetholone is a 17α-alkylated dihydrotestosterone (DHT) derivative. This structural modification (alkylation at the 17th carbon) allows the molecule to survive first-pass metabolism in the liver, granting it high oral bioavailability. This same feature is also primarily responsible for its significant hepatotoxicity potential.

Mechanism of Action:

  • Androgen Receptor (AR) Agonism: Like all AAS, Oxymetholone binds to and activates intracellular androgen receptors. This complex then translocates to the cell nucleus, influencing gene transcription to promote nitrogen retention, protein synthesis, and inhibition of protein catabolism.

  • Erythropoiesis Stimulation: A key feature of Oxymetholone is its potent stimulation of erythropoietin (EPO) production, likely via both direct renal effects and possibly enhanced sensitivity of bone marrow erythroid progenitor cells to endogenous EPO. This leads to a marked increase in red blood cell count and hemoglobin levels.

  • Anabolic vs. Androgenic Ratio: While all AAS possess both properties, Oxymetholone is clinically observed to have a pronounced anabolic effect relative to its androgenic effects (such as virilization) when used at therapeutic doses for anemia. This does not eliminate androgenic side effects but highlights its tissue-building and RBC-stimulating potency.

Pharmacokinetics:

  • Absorption: Well absorbed from the gastrointestinal tract due to its 17α-alkylated structure.

  • Metabolism: Extensively metabolized in the liver by various cytochrome P450 enzymes.

  • Half-life & Excretion: The half-life is estimated between 9-16 hours, supporting a typical clinical dosing regimen of 1-5 mg per kilogram of body weight per day, often divided into multiple doses. It is excreted primarily in the urine as metabolites.

Dosage, Administration, and Important Considerations

  • Standard Medical Dosage: For adults with aplastic anemia, the typical starting dose ranges from 1 to 5 mg per kilogram of body weight per day. The 25mg tablet strength allows for flexible and precise titration by a physician. Treatment is often administered chronically over several months, with regular monitoring for efficacy and toxicity.

  • Administration: Tablets should be taken with food to potentially minimize gastric upset. Compliance with the prescribed split-dosing schedule is essential for stable blood levels.

  • Monitoring is Paramount: Any legitimate therapeutic use of ANADROL 25 mandates rigorous medical supervision, including:

    • Weekly to Monthly Blood Tests: Complete Blood Count (CBC) to monitor hematocrit/hemoglobin (risk of polycythemia), liver function tests (LFTs: AST, ALT, Bilirubin, Alkaline Phosphatase), and lipid profiles (cholesterol/triglycerides).

    • Clinical Evaluation: Regular check-ups for blood pressure, signs of fluid retention, virilization in women, prostatic hypertrophy in men, and mental health status.

Contraindications and Serious Health Warnings

ANADROL 25 is absolutely contraindicated in patients with:

  • Known hypersensitivity to Oxymetholone.

  • Men with carcinoma of the prostate or breast.

  • Women with carcinoma of the breast (unless treating progressive disease after menopause).

  • Pregnancy and Nursing Mothers: Can cause severe fetal virilization.

  • Serious pre-existing liver disease (e.g., cirrhosis, hepatitis) or impaired liver function.

  • Hypercalcemia (in patients with breast cancer).

  • Severe cardiac, renal, or hepatic dysfunction.

  • Nephrosis or the nephrotic phase of nephritis.

Comprehensive Side Effect Profile

Due to its potency, the side effects of Oxymetholone can be severe and must be thoroughly understood:

  • Hepatotoxicity: This is the most significant risk with 17α-alkylated oral AAS. Effects range from reversible hepatic transaminase elevations and cholestatic jaundice to rare but life-threatening peliosis hepatis (blood-filled cysts in the liver), hepatic tumors, and hepatic failure.

  • Cardiovascular: Hypertension, edema (due to water and sodium retention), and detrimental shifts in lipid profile (decreased HDL, increased LDL cholesterol), increasing long-term atherosclerosis risk.

  • Hematologic: Polycythemia (excess RBCs), increasing the risk of thrombosis, stroke, and myocardial infarction.

  • Endocrine & Reproductive:

    • In Men: Testicular atrophy, oligospermia/azoospermia (infertility), gynecomastia (breast tissue development), impotence, and priapism.

    • In Women: Virilization is common and often irreversible: deepening of the voice, clitoral enlargement, hirsutism (excessive body/facial hair), menstrual irregularities, and male-pattern baldness.

  • Other: Acne, premature epiphyseal closure in adolescents, insomnia, aggression, depression, and prostate hypertrophy.

Conclusion: A Specialized Tool for Specific Clinical Challenges

GenLabs' ANADROL 25 (Oxymetholone 25mg) represents a specialized, high-potency pharmaceutical agent with a defined and narrow role in clinical medicine. Its profound ability to stimulate red blood cell production and promote anabolism makes it a valuable, though high-risk, option for managing severe, refractory anemias due to bone marrow failure. The 200-tablet presentation is designed for sustained clinical treatment protocols under continuous medical oversight.

The cornerstone of its use is the fundamental principle of medical ethics: a careful risk-benefit analysis conducted by a specialist physician, paired with relentless patient monitoring. This description underscores that ANADROL 25 is a powerful medication with a formidable side-effect profile, strictly reserved for legitimate therapeutic contexts defined by law and medical practice. GenLabs provides this compound to meet specific clinical needs, emphasizing that patient safety and informed, supervised use are the absolute priorities.

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Genlabs BPC-157 – 20mg/Vial: The Premier Systemic Repair Peptide for Advanced Research

Product Name: Genlabs BPC-157 – 20mg/Vial (with Bacteriostatic Water)
SKU: GL-BPC157-20
Catalog: Research Peptides


Introduction: Redefining the Frontier of Systemic Recovery Research

In the rigorous field of research peptides, few compounds have generated as much scientific interest for their broad-spectrum systemic properties as BPC-157. Genlabs, a name synonymous with precision and purity, presents its flagship BPC-157 – 20mg/Vial, meticulously synthesized and paired with sterile Bacteriostatic Water. This high-concentration formulation is designed for the discerning researcher seeking to investigate the remarkable regenerative and protective mechanisms of this stable peptide fragment. Our 20mg vial offers exceptional value and flexibility, allowing for precise dosing regimens in controlled experimental settings focused on musculoskeletal, gastrointestinal, and systemic inflammatory responses.

Genlabs’ commitment to excellence ensures every batch is verified for >99% purity, is sterile-filtered, and undergoes independent third-party analysis (COA available). This product is presented strictly for in-vitro and research applications in laboratory settings.


What is BPC-157? A Scientific Overview

BPC-157 (Body Protection Compound-157) is a synthetic peptide sequence comprising 15 amino acids, derived from a protective protein found in human gastric juice. Unlike larger, more fragile proteins, this pentadecapeptide is renowned for its exceptional stability and systemic effects in research models. It is not a growth hormone or a steroid; rather, it is characterized as a "protective modulator" with a unique mechanism of action centered on promoting cellular survival, angiogenesis (formation of new blood vessels), and tissue repair across a wide range of systems.

Its proposed research profile suggests it operates through several key pathways: promoting VEGF (Vascular Endothelial Growth Factor) expression for improved blood flow to injured sites, modulating inflammatory cytokine responses to maintain a balanced healing environment, and stimulating the synthesis of collagen and other structural proteins. This multi-modal approach has made BPC-157 a subject of extensive preclinical investigation.


Genlabs BPC-157 – 20mg: Key Features & Advantages

  1. Uncompromising Purity & Verification: Each batch is synthesized using state-of-the-art solid-phase peptide synthesis (SPPS) and undergoes rigorous HPLC (High-Performance Liquid Chromatography) and MS (Mass Spectrometry) testing. The certificate of analysis confirms a purity level of >99%, ensuring your research is not compromised by contaminants or filler peptides.

  2. Optimal Concentration & Format: The 20mg per vial format is ideal for extended research protocols. This substantial quantity provides researchers with ample material for longitudinal studies or higher-dose investigations without frequent replenishment, ensuring consistency across the experimental timeline.

  3. Included Bacteriostatic Water: Each order includes a separate vial of sterile, USP-grade 0.9% Bacteriostatic Sodium Chloride Injection (containing 0.9% benzyl alcohol). This eliminates the need for separate sourcing and guarantees compatibility, making the reconstitution process seamless and aseptic.

  4. Lyophilized for Maximum Stability: The peptide is provided in a stable, freeze-dried (lyophilized) powder form within a sterile glass vial. This preservation method ensures long-term stability when stored correctly, protecting the integrity of the molecular structure until reconstitution.

  5. Sterile-Filtered & Prepared in a cGMP-Compliant Facility: Our manufacturing process adheres to current Good Manufacturing Practices (cGMP). The solution is sterile-filtered through a 0.22-micron filter before lyophilization, a critical step to ensure sterility and researcher safety.

  6. Comprehensive Third-Party Testing: Beyond in-house QC, samples from every lot are sent to an independent, ISO-certified laboratory for confirmatory analysis. The resulting Certificate of Analysis (COA) is transparently available, providing verified data on purity, weight, and absence of endotoxins or microbial growth.


Primary Research Applications & Investigative Pathways

*Disclaimer: The following are well-documented areas of scientific inquiry based on preclinical studies. Genlabs BPC-157 is sold for laboratory research use only.*

  • Musculoskeletal & Tendon-Ligament Repair: A primary focus of BPC-157 research is its potential to accelerate the healing of various connective tissues. Studies have investigated its effects on models of tendon-to-bone healing, muscle fiber regeneration, and ligament repair. Its proposed angiogenic and collagen-stimulating properties are of particular interest in this domain.

  • Gastrointestinal System Protection & Healing: Given its origin, significant research explores BPC-157's protective effects on the GI tract. Investigations include models of gastric ulcers, inflammatory bowel conditions, and intestinal anastomosis healing. It is studied for its potential to promote mucosal integrity and modulate local blood flow.

  • Systemic Anti-Inflammatory Modulation: Researchers examine BPC-157's role in influencing systemic inflammatory responses. Its interaction with key inflammatory pathways (e.g., TNF-alpha, COX-2) is a subject of interest for creating a balanced cellular environment conducive to recovery.

  • Organ Protection & Support: Emerging research vectors include investigating BPC-157's potential protective effects on the liver (in toxin-exposed models), heart (in ischemia-reperfusion injury models), and nervous system.

  • Angiogenesis & Wound Healing: The peptide's strong association with promoting VEGF-driven angiogenesis places it at the center of wound healing research, particularly in models of impaired healing or compromised blood supply.


Reconstitution, Storage, and Handling Protocol

Storage (Lyophilized Powder): Store immediately upon receipt in a freezer at -20°C or below. For long-term storage (over 6 months), a temperature of -80°C is recommended. Keep the vial in its original desiccated state and protected from light.

Reconstitution:

  1. Gently swirl the vial of Bacteriostatic Water to mix.

  2. Using aseptic technique, draw the desired volume of bacteriostatic water into a sterile syringe.

  3. Slowly inject the water down the side of the vial containing the BPC-157 lyophilized powder. Avoid directing a high-pressure stream directly onto the powder.

  4. Gently swirl or roll the vial until the powder is fully dissolved. Do not shake vigorously, as this can cause denaturation of the peptide.

Storage (Reconstituted Solution): Once reconstituted with bacteriostatic water (which contains a preservative), the solution should be refrigerated at 2-8°C (36-46°F). Under these conditions, stability is typically maintained for up to 21 days. For optimal potency, many researchers prefer to use the solution within 7-10 days. Aliquotting into smaller, sterile vials can minimize repeated freeze-thaw cycles if freezing the reconstituted solution is necessary.


Why Choose Genlabs for Your Peptide Research?

Genlabs stands apart in the research peptide industry through an unwavering dedication to scientific integrity:

  • Transparency is Paramount: We provide batch-specific, third-party COAs, not generic datasheets.

  • Purity-First Philosophy: Our >99% purity standard is non-negotiable, ensuring reliable and reproducible research outcomes.

  • Researcher-Centric Formatting: The inclusion of bacteriostatic water and high-concentration vials is designed for convenience and experimental flexibility.

  • Compliance & Ethics: We operate with strict adherence to legal and ethical guidelines, supplying products exclusively to verified research institutions and qualified professionals for laboratory investigation.

Product Specifications:

  • Sequence: Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val

  • Molecular Formula: C₆₂H₉₈N₁₆O₂₂

  • Molecular Weight: 1419.5 g/mol

  • Purity: >99% (by HPLC)

  • Form: Lyophilized white powder

  • Packaging: 20mg peptide in sterile glass vial + 2ml bacteriostatic water (0.9% BA) in separate vial.



Cialis is a prescription medication that is primarily used to treat erectile dysfunction (ED) in adult men. It belongs to a class of drugs called phosphodiesterase type 5 (PDE5) inhibitors. The active ingredient in Cialis is tadalafil.

Cialis works by increasing blood flow to the penis during sexual stimulation, which helps men achieve and maintain an erection. Unlike other ED medications, Cialis has a longer duration of action, often referred to as the "weekend pill," as it can provide up to 36 hours of effectiveness.

When taken as directed, Cialis is typically available in tablet form, with various strengths ranging from 2.5mg to 20mg. The recommended starting dose for most men is 10mg, which can be adjusted based on individual response and tolerability. It is important to follow the prescribed dosage instructions and not exceed the recommended dose.

It is worth noting that Cialis does not cause an erection on its own; sexual stimulation is still required for the medication to work effectively. Additionally, Cialis should not be taken more than once a day.

While primarily used for treating ED, Cialis also has another approved use for the treatment of benign prostatic hyperplasia (BPH), a condition characterized by an enlarged prostate gland. In this case, Cialis helps relax the muscles in the prostate and bladder, leading to improved urine flow and reduced symptoms associated with BPH.

As with any medication, Cialis may have potential side effects. Common side effects include headache, indigestion, back pain, muscle aches, flushing, and stuffy or runny nose. These side effects are usually mild and temporary.

However, it is essential to seek medical attention if you experience more severe side effects such as chest pain, vision changes, sudden hearing loss, or a prolonged erection lasting more than four hours (priapism), as these may require immediate medical attention.

Cialis should only be taken under the supervision of a healthcare professional, who will evaluate your medical history, current medications, and overall health to determine if it is suitable for you. It is crucial to disclose any existing medical conditions or medications you are taking to ensure the safe use of Cialis.

In summary, Cialis is a prescription medication used to treat erectile dysfunction and benign prostatic hyperplasia. It helps improve blood flow to the penis, resulting in enhanced sexual performance. However, it is essential to use Cialis as directed and consult a healthcare professional for proper evaluation and guidance.



FRAG-176 5MG VIAL (with Bacteriostatic Water) – GENLABS: The Definitive Guide to Advanced Metabolic Enhancement

Product Name: FRAG-176 5mg Vial (with Bacteriostatic Water)
Brand: GENLABS
Active Ingredient: Fragment 176-191 (FRAG-176), a modified, selective segment of Human Growth Hormone (HGH).
Presentation: Sterile lyophilized powder in a 5mg vial, accompanied by a separate 2ml vial of Bacteriostatic Water for reconstitution.
Primary Applications: Targeted fat metabolism, stubborn adipose tissue reduction, metabolic optimization, and body recomposition.


Introducing FRAG-176 by GENLABS: Precision Science for Targeted Fat Loss

In the pursuit of optimal body composition, the challenge has never been merely about weight loss—it’s about the precise, targeted reduction of stubborn adipose tissue that resists diet and exercise. GENLABS rises to this challenge with FRAG-176, a pinnacle of peptide science designed for researchers and enthusiasts seeking a sophisticated approach to metabolic enhancement. Unlike broad-spectrum compounds, FRAG-176 represents a paradigm shift: a selective, fragment-based therapy that harnesses the fat-mobilizing power of Growth Hormone without its systemic proliferative effects.

Our FRAG-176 5mg Vial, complete with convenient Bacteriostatic Water, embodies the GENLABS commitment to purity, precision, and research excellence. This product is meticulously synthesized in state-of-the-art cGMP-certified facilities, undergoes rigorous third-party HPLC/MS analysis for verification of >99% purity, and is presented in sterile, lyophilized form to ensure stability and potency. It is crafted for the discerning individual who demands nothing less than laboratory-grade quality for their investigative work in metabolic function and adipose tissue biology.

Understanding the Molecule: What is FRAG-176?

FRAG-176, also known as AOD-9604 (Anti-Obesity Drug 9604), is a synthetic peptide fragment comprising the 176-191 amino acid sequence of the Human Growth Hormone (HGH) beta chain. This region has been identified in scientific literature as the "lipolytic region" – the key segment responsible for HGH's ability to stimulate fat breakdown (lipolysis) and inhibit fat storage (lipogenesis).

The genius of FRAG-176 lies in its modification and selectivity. While full-sequence HGH influences growth in bones, organs, and muscles via IGF-1 mediation, the FRAG-176 fragment has been specifically engineered to disconnect fat-burning from growth promotion. It operates through a direct, receptor-mediated mechanism on adipose (fat) cells, making it a highly targeted agent for metabolic research. It does not significantly impact blood sugar (insulin resistance) or promote growth in non-adipose tissues, a significant distinction from its parent molecule.

Key Research Applications and Potential Benefits

GENLABS FRAG-176 is intended for in vitro and research applications to study the following areas:

  1. Targeted Lipolysis: The primary research focus is on the peptide's ability to selectively stimulate the breakdown of stored triglycerides in adipocytes (fat cells), particularly within stubborn fat deposits such as the abdomen, waist, and thighs.

  2. Inhibition of Lipogenesis: Research indicates FRAG-176 may help suppress the conversion of excess carbohydrates into stored fat, studying its role in regulating the body's fat-storage pathways.

  3. Metabolic Rate Enhancement: Investigations explore how FRAG-176 can influence the basal metabolic rate (BMR), potentially increasing the body's innate caloric expenditure, even at rest.

  4. Improved Body Composition & Recomposition: A core area of study is its potential to alter the fat-to-lean mass ratio, supporting research into protocols aimed at reducing adipose tissue while preserving lean muscle mass—a critical goal in body recomposition.

  5. Appetite Modulation: Preliminary studies suggest a potential role in influencing hormones related to satiety and hunger, such as leptin, making it a compound of interest for research into metabolic signaling pathways.

Why Choose GENLABS FRAG-176? Our Commitment to Excellence

  • >99% HPLC/MS Verified Purity: Every batch is independently analyzed, with certificates of analysis (CoA) available, confirming the absence of impurities and accurate peptide content.

  • cGMP Synthesis: Manufactured under strict Current Good Manufacturing Practices, ensuring the highest standards of production, sterility, and consistency.

  • Lyophilized for Maximum Stability: The freeze-dried powder format guarantees long-term stability and potency until the moment of reconstitution.

  • Supplied with Bacteriostatic Water: We include a sterile 2ml vial of Bacteriostatic Water (0.9% Benzyl Alcohol), simplifying the preparation process and ensuring multi-dose usability post-reconstitution for 28 days.

  • Research-Focused Formulation: Designed explicitly for laboratory use, our product is free from unnecessary additives, providing researchers with the pure compound for their studies.

  • Vacuum-Sealed Vials: Each vial is sealed under vacuum, a key indicator of proper manufacturing and sterility. You will hear the distinct "hiss" upon puncturing the rubber stopper.

Laboratory Handling and Preparation Guide

Materials Provided: 1 x 5mg FRAG-176 lyophilized vial, 1 x 2ml Bacteriostatic Water vial.
Materials Required (Not Included): Sterile alcohol wipes, sterile insulin syringes (1ml or 0.5ml, measured in IU), appropriate sharps disposal container.

Reconstitution Protocol:

  1. Sanitize: Clean the rubber stoppers of both vials thoroughly with an alcohol wipe.

  2. Draw Bacteriostatic Water: Draw 1-2ml of the supplied Bacteriostatic Water into a sterile syringe. (1ml is standard for a concentration of 5mg/ml).

  3. Reconstitute: Gently inject the water into the FRAG-176 vial, aiming the stream against the glass wall to avoid aggressive agitation of the peptide. Swirl the vial gently until the powder is fully dissolved into a clear liquid. Do not shake.

  4. Storage: Once reconstituted, the solution must be stored refrigerated at 2°C to 8°C (36°F to 46°F) and used within 28 days due to the preservative in the Bacteriostatic Water. Unreconstituted vials should be stored in a cool, dark place.

Important Research Considerations:

  • Sterility is Paramount: All handling must be performed in a clean, aseptic manner to prevent microbial contamination.

  • Dosage is Research-Dependent: Concentration and dosing volume are determined by specific research design parameters. Common research protocols often investigate doses in the range of 250-500mcg per day.

  • Site of Study: Research often involves subcutaneous administration models for study.

  • Consult Literature: Researchers are advised to base their protocols on existing, published scientific literature on Fragment 176-191.

Frequently Asked Questions (FAQ)

Q: Is FRAG-176 the same as HGH?
A: No. FRAG-176 is a fragment of the HGH molecule. It mimics the fat-burning actions of HGH but has been shown in studies to lack its growth-promoting and potentially insulin-disrupting effects.

Q: How long does a 5mg vial last in a research setting?
A: This depends entirely on the experimental protocol. For example, a daily research dose of 500mcg would utilize one 5mg vial over approximately 10 study days.

Q: Why is Bacteriostatic Water included?
A: Bacteriostatic Water contains 0.9% Benzyl Alcohol, which inhibits bacterial growth. This allows the reconstituted solution to be used safely in a multi-dose model for up to 28 days when refrigerated, which is essential for research efficiency.

Q: What are the expected research outcomes?
A: Research focuses on outcomes related to enhanced lipolytic activity, reduced adipocyte size, changes in metabolic rate markers, and alterations in body composition metrics. Results are protocol and subject-dependent.

Q: Is this product for human consumption?
A: No. GENLABS FRAG-176 is sold strictly for laboratory research purposes only. It is not a drug, dietary supplement, or intended for diagnostic or therapeutic use. It is not for human or animal consumption. This product is to be used only by qualified researchers in controlled laboratory settings.

Conclusion: Elevate Your Metabolic Research with GENLABS

For the serious researcher investigating the frontiers of metabolic science and targeted lipolysis, GENLABS FRAG-176 offers an unmatched tool. It combines cutting-edge peptide technology with an unwavering commitment to quality and purity. By focusing on the precise mechanism of action within adipose tissue, FRAG-176 opens a window into sophisticated body recomposition strategies.

Choose GENLABS FRAG-176 5mg Vial—where exceptional quality meets pioneering science. Explore the potential of targeted metabolic enhancement with a compound built on a foundation of verified purity and research-grade excellence.

Disclaimer: This information is for educational and research purposes only. This product is a chemical for laboratory research and is not intended for human or veterinary diagnostic or therapeutic use. The researcher assumes all liability for the safe handling, storage, and use of this product in compliance with all applicable local, state, and federal regulations.



Kisspeptin-5mg (with Bacteriostatic Water) – GenLabs | A Premium Neuropeptide for Endocrine System Research

In the evolving landscape of biochemical research and advanced endocrine studies, Kisspeptin has emerged as a fundamental neuropeptide of profound scientific interest. GenLabs, a name synonymous with precision and purity in peptide science, presents its meticulously formulated Kisspeptin-5mg, complete with a complimentary vial of Bacteriostatic Water. This product is engineered for the exacting demands of clinical research environments, offering researchers a reliable, high-purity tool to explore the intricate pathways of the hypothalamic-pituitary-gonadal (HPG) axis.

This comprehensive description details the science of Kisspeptin, the unparalleled quality of the GenLabs formulation, its primary research applications, and the critical importance of its pairing with bacteriostatic water for optimal reconstitution and stability.

Understanding Kisspeptin: The Master Regulator of GnRH

Kisspeptin, encoded by the KISS1 gene, is a potent endogenous neuropeptide that acts as the primary upstream stimulator of Gonadotropin-Releasing Hormone (GnRH) neurons. Its discovery revolutionized the understanding of reproductive physiology. By binding with high affinity to its receptor, GPR54 (Kiss1R), Kisspeptin triggers a cascade that results in the pulsatile secretion of GnRH. This, in turn, stimulates the anterior pituitary gland to release Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH), the key drivers of gonadal function and sex steroid hormone production (estrogen, progesterone, testosterone).

GenLabs' Kisspeptin-5mg typically refers to the Kisspeptin-10 fragment (KP-10), the shortest fully bioactive sequence (amino acids 112-121 of the full protein). This decapeptide retains full biological activity, making it an efficient and potent agent for research purposes.

GenLabs Commitment: Purity, Stability, and Authenticity

Every batch of GenLabs Kisspeptin-5mg is a testament to our rigorous quality assurance protocols.

  • High-Purity Synthesis: Produced using state-of-the-art solid-phase peptide synthesis (SPPS), our Kisspeptin undergoes extensive purification via High-Performance Liquid Chromatography (HPLC) to achieve a purity grade of ≥98%. This minimizes the presence of truncated sequences or impurities that could skew research data.

  • Mass Spectrometry (MS) Verification: Each vial’s contents are confirmed through mass spectrometry analysis, ensuring the correct molecular weight and amino acid sequence, guaranteeing you receive the authentic, bioactive peptide.

  • Sterile, Lyophilized Form: The peptide is provided as a sterile, lyophilized (freeze-dried) white powder in a sealed, nitrogen-flushed glass vial to ensure long-term stability and prevent degradation prior to reconstitution.

  • Complimentary Bacteriostatic Water: Included is a vial of sterile Bacteriostatic Water (0.9% Benzyl Alcohol). This is not just a convenience but a necessity. The bacteriostatic agent inhibits bacterial growth in the reconstituted solution, allowing for multi-dose use over a period of time (typically up to 28 days when refrigerated) while maintaining sterility and peptide integrity.

Primary Areas of Research Interest

GenLabs' Kisspeptin-5mg is intended for in vitro and preclinical research applications within controlled laboratory settings. Its primary research applications focus on:

  1. Reproductive Endocrinology Research: As the key initiator of the HPG axis, Kisspeptin is a critical tool for studying pubertal development, gonadal steroid feedback mechanisms, and the pulsatile nature of gonadotropin secretion. Research investigates its role in conditions like hypogonadotropic hypogonadism.

  2. Neuroendocrine Signaling Studies: Scientists utilize Kisspeptin to map and understand the complex neural circuits that control reproduction, including the interaction between metabolic signals (like leptin) and reproductive function.

  3. Fertility-Related Investigations: Research explores the potential of Kisspeptin as a more physiological trigger for ovulation in assisted reproductive technology (ART) contexts, given its role in inducing endogenous GnRH/LH surges.

  4. Metabolic and Reproductive Interface Studies: Given the link between energy balance and fertility, Kisspeptin serves as a primary research target for understanding how conditions like obesity or anorexia impact reproductive function.

  5. Pharmacodynamic/Pharmacokinetic Studies: The GenLabs formulation is ideal for studies examining the half-life, bioavailability, and dose-response characteristics of Kisspeptin-10 administration.

Reconstitution and Handling Protocol

Proper reconstitution is vital for maintaining peptide bioactivity and sterility.

  1. Aseptic Technique: Perform all steps in a clean, laminar flow hood using sterile syringes, needles, and gloves.

  2. Reconstitution: Gently inject the desired volume of the supplied bacteriostatic water (e.g., 1-2 mL) slowly down the side of the peptide vial to avoid aggressive agitation. Roll the vial gently between your hands until the lyophilized powder is fully dissolved. Do not shake vigorously, as this can cause peptide denaturation.

  3. Storage: The reconstituted solution should be stored at 2-8°C (36-46°F) and used within the appropriate timeframe as dictated by laboratory sterility protocols. The lyophilized powder, unopened, should be stored in a cool, dry place, away from direct light.

  4. Dosage Considerations: Research dosage is highly dependent on the specific model and study design. Researchers must determine appropriate concentrations based on existing scientific literature and pilot studies.

Why Choose GenLabs Kisspeptin-5mg?

  • Integrated Research Solution: The inclusion of bacteriostatic water ensures you have everything needed to begin research immediately, prepared to the highest sterility standards.

  • Documented Purity: Access to a Certificate of Analysis (CoA) for your specific lot, detailing HPLC purity, mass spec confirmation, and sterility testing.

  • Manufacturing Transparency: GenLabs operates in cGMP-compliant facilities, ensuring traceability and consistency from synthesis to shipment.

  • Research Reliability: Consistent, high-quality peptide structure ensures reproducible results, reducing experimental variables and enhancing the credibility of your research outcomes.

  • Dedicated Support: Our commitment extends beyond the product. We provide comprehensive technical data sheets and support for qualified research professionals.

Important Disclaimer

GenLabs Kisspeptin-5mg (with Bacteriostatic Water) is sold strictly for research and laboratory use only. It is classified as a Research Chemical. It is not intended for human or veterinary diagnostic, therapeutic, or any other clinical uses. It must not be introduced into food or drink products or household chemicals. The information contained herein is for educational and scientific reference purposes only.

Researchers assume full responsibility for handling this product in accordance with all applicable local, state, federal, and institutional guidelines and regulations. Proper personal protective equipment (PPE) must always be worn when handling.



Nandrolone phenylpropionate, also known as NPP, is an anabolic androgenic steroid (AAS) that belongs to the family of nandrolone compounds. It is a modified form of testosterone with an attached phenylpropionate ester, which alters its pharmacokinetics and provides a shorter half-life compared to other nandrolone esters.

NPP is primarily used in the medical field for various therapeutic purposes. It has been prescribed to treat conditions such as osteoporosis, muscle wasting diseases, and certain forms of anemia. Additionally, it has been used to enhance recovery from injuries and surgeries, aiding in the regeneration and repair of tissues.

From a performance-enhancing perspective, NPP is popular among bodybuilders and athletes due to its ability to promote muscle growth and enhance physical performance. It exhibits strong anabolic properties while having a relatively lower androgenic effect compared to testosterone, making it a favorable choice for those seeking gains in lean muscle mass without excessive androgenic side effects.

NPP works by binding to androgen receptors in the body, stimulating protein synthesis and nitrogen retention, which are essential for muscle growth and recovery. It also increases the production of red blood cells, improving oxygen-carrying capacity and endurance. These effects contribute to enhanced strength, increased muscle size, and improved athletic performance.

As with any AAS, NPP carries potential side effects. Some common androgenic side effects include oily skin, acne, and increased facial or body hair growth. It can also suppress natural testosterone production, leading to temporary infertility or testicular atrophy. Additionally, it may cause cardiovascular issues, such as increased cholesterol levels and high blood pressure, and can have adverse effects on liver function.

Proper administration and dosage are essential to minimizing the risks associated with NPP. It is typically administered through intramuscular injections, with dosages ranging from 50mg to 100mg every other day or every three days. The duration of NPP cycles can vary, typically lasting between 6 to 12 weeks.

It is important to note that the use of NPP, or any other AAS, without proper medical supervision is considered illegal and potentially dangerous. Misuse or abuse of these substances can result in serious health consequences and may violate anti-doping regulations in sports.

If you are considering using NPP or any other AAS, it is crucial to consult with a qualified healthcare professional who can provide guidance, monitor your health, and ensure your safety throughout the process.



Unlock Peak Vitality: A Comprehensive Guide to Cinnatropin (Somatropin 30IU) HGH Pen

In the pursuit of optimized health, performance, and longevity, bio-identical human growth hormone (HGH) stands as a cornerstone of modern endocrine therapy. Cinnatropin (Somatropin 30IU) 10mg/1.5ml – HGH Pen represents the pinnacle of this science—a precision-engineered, recombinant DNA-derived somatropin delivery system designed for unmatched efficacy, safety, and user convenience. This is not merely a medication; it is a sophisticated tool for metabolic rejuvenation, trusted by medical professionals and under strict regulatory oversight for prescribed use.

What is Cinnatropin (Somatropin)?

Cinnatropin is the brand name for a biosynthetic form of somatropin, which is identical in structure to the 191-amino acid sequence of endogenous human growth hormone produced by the pituitary gland. Manufactured using advanced recombinant DNA technology, it guarantees purity, consistency, and biological activity free from human-derived contaminants. The 30IU (10mg) formulation in a concentrated 1.5ml solution provides a potent and lasting supply, housed within a state-of-the-art, multi-dose injection pen.

Indications & Therapeutic Applications

Cinnatropin is a prescription pharmaceutical indicated for the treatment of growth hormone deficiency (GHD) and associated conditions. Its primary uses include:

  • Adult Growth Hormone Deficiency (AGHD): Characterized by decreased energy, reduced bone density, unfavorable changes in body composition (increased adipose tissue, decreased muscle mass), dyslipidemia, and diminished quality of life. Cinnatropin therapy works to reverse these symptoms.

  • Pediatric Growth Hormone Deficiency (PGHD): For children with insufficient endogenous HGH production, leading to growth failure. Treatment promotes linear growth and development.

  • Turner Syndrome: A genetic condition in females where HGH therapy is used to improve growth outcomes.

  • Chronic Renal Insufficiency (CRI) in Children: To counteract growth impairment prior to kidney transplantation.

  • Prader-Willi Syndrome (with confirmed GHD): To improve body composition and physical capacity in affected children.

Important Notice: Cinnatropin is a potent prescription-only medication. It must be used under the continuous supervision of a qualified healthcare professional who will conduct thorough diagnostic testing (including IGF-1 level assessments and stimulation tests) to confirm deficiency and establish the correct, individualized dosage. It is not indicated for anti-aging, athletic enhancement, or weight loss in individuals without a confirmed clinical deficiency.

Key Features & Benefits of the Cinnatropin HGH Pen

1. Pharmaceutical-Grade Purity & Potency:
Each pen contains precisely 30 International Units (IU), equivalent to 10 milligrams, of 99%+ pure somatropin. This ensures predictable biological activity and consistent therapeutic results with every dose, batch after batch.

2. Advanced Pen Delivery System:
The pre-filled, multi-dose injection pen revolutionizes the administration of HGH.

  • Precision Dosing: Features a clear dose selector with audible clicks, allowing for accurate micro-adjustments as prescribed by your physician.

  • Enhanced Comfort: Utilizes ultra-fine, short needles (typically 29-32 gauge) for a near-painless subcutaneous injection experience, reducing anxiety and improving adherence.

  • Convenience & Discretion: The pen is pre-filled and ready to use, eliminating the need for vial reconstitution and syringe drawing. It’s portable and discreet for travel or daily use.

  • Safety: Built-in mechanisms help prevent dosing errors and needlestick injuries.

3. Concentrated 1.5ml Formulation:
The 30IU potency is delivered in a minimal volume (1.5ml), resulting in a highly concentrated solution. This allows for a smaller injection volume, which is associated with greater patient comfort and reduced risk of local injection site reactions.

4. Clinically Proven Outcomes:
When prescribed correctly for deficiency, patients report significant improvements across multiple parameters:

  • Body Composition: Marked reduction in visceral and subcutaneous adipose tissue, with a concurrent increase in lean muscle mass.

  • Bone Metabolism: Improved bone mineral density, strengthening the skeletal framework and reducing fracture risk.

  • Cardiometabolic Profile: Positive effects on lipid metabolism (reduced LDL, increased HDL) and improved cardiac output.

  • Skin & Hair Quality: Enhanced skin thickness, elasticity, and hydration, alongside improved hair growth.

  • Psychological Well-being: Documented improvements in energy levels, exercise capacity, mood, and overall quality of life.

Administration & Storage Guidelines

  • Administration: Cinnatropin is administered via subcutaneous injection (into the fatty tissue under the skin), typically in the abdomen, thighs, or buttocks, with rotation of sites. Your physician will provide comprehensive training on proper pen use, injection technique, and dose calculation.

  • Dosage: Extremely individualized. The starting dose for adults is often very low (e.g., 0.1 to 0.3 mg/day) and carefully titrated based on clinical response, IGF-1 levels, and side effect tolerance. Never self-adjust your dosage.

  • Storage:

    • Unopened Pens: Must be stored refrigerated at 2°C to 8°C (36°F to 46°F). Do not freeze. Protect from light.

    • In-Use Pen: Once a pen is started, it may typically be kept at room temperature (not to exceed 25°C/77°F) for up to 21-28 days—refer to the specific manufacturer's leaflet. Always recap the pen and keep it out of direct sunlight and heat.

Potential Side Effects & Contraindications

Like all potent therapeutics, Cinnatropin may cause side effects, which are often dose-dependent and may subside with dose adjustment.

  • Common Side Effects: Injection site reactions (redness, swelling), peripheral edema (fluid retention), arthralgia (joint pain), myalgia (muscle pain), paresthesia (tingling), and headaches.

  • Serious Side Effects (Require Immediate Medical Attention): Carpal tunnel syndrome, severe persistent headaches with visual changes (indicative of intracranial hypertension), signs of glucose intolerance, and severe allergic reactions. In adults, there is a theoretical increased risk of malignancy, which your doctor will monitor for.

  • Contraindications: Active malignancy, proliferative or severe non-proliferative diabetic retinopathy, acute critical illness due to complications after open heart or abdominal surgery, multiple accidental trauma, or acute respiratory failure. It is also contraindicated in patients with known hypersensitivity to somatropin or any excipients in the pen.

Why Choose Cinnatropin HGH Pen?

Choosing Cinnatropin is choosing a gold standard in growth hormone therapy. It combines the biological fidelity of pure somatropin with the unparalleled ease and accuracy of a modern pen device. For the patient with a genuine deficiency, this translates to a treatment that is not only effective in restoring physiological balance but also seamlessly integrates into daily life, maximizing compliance and, ultimately, long-term health outcomes.

Disclaimer: This information is for educational purposes only and does not constitute medical advice. Human Growth Hormone is a controlled prescription substance. The diagnosis of Growth Hormone Deficiency and treatment with Cinnatropin must be managed by a licensed endocrinologist or qualified healthcare provider. Unauthorized purchase or use without a prescription is illegal and dangerous.

Consult your healthcare provider to determine if your symptoms align with Growth Hormone Deficiency and to discuss whether a therapy like Cinnatropin could be a safe and appropriate part of your personalized treatment plan.



LIV.52 Syrup | Natural Liver Protection & Detoxification | 100ml Bottle – Himalaya

In today’s world, our liver—the body's premier detoxification engine—faces an unprecedented barrage of challenges. From environmental pollutants and processed foods to occasional dietary indiscretions, hepatic strain is a common, yet often overlooked, health concern. A compromised liver can manifest as fatigue, poor digestion, sluggish metabolism, and loss of appetite. Introducing Himalaya LIV.52 Syrup, a time-tested and scientifically validated Ayurvedic formulation meticulously crafted to offer comprehensive hepatic support. More than just a liver tonic, LIV.52 Syrup is a holistic wellness solution designed to protect the liver against various hepatotoxins, promote healthy appetite, and support optimal growth and development in children and adults. Encased in this 100ml bottle is over six decades of Ayurvedic wisdom backed by modern research, offering a natural shield for your body's vital metabolic organ.

Understanding Liver Health and the Need for Protection
The liver is a metabolic powerhouse responsible for over 500 critical functions, including detoxification (filtering toxins from the blood), metabolism (processing fats, proteins, and carbohydrates), synthesis of essential proteins and digestive bile, and storage of vital nutrients. When liver function is suboptimal, these processes are disrupted, leading to a cascade of health issues. LIV.52 Syrup targets the root cause by fortifying the liver's own defense and repair mechanisms, ensuring it performs its duties efficiently. This proactive support is crucial for maintaining overall vitality in the face of daily environmental and dietary stressors.

Comprehensive Benefits of Himalaya LIV.52 Syrup

Advanced Hepatoprotection: A Shield for Liver Cells
The primary and most researched benefit of LIV.52 Syrup is its profound ability to safeguard liver cells, or hepatocytes. The unique blend of herbs acts synergistically to provide a multi-layered defense. It offers a protective effect against various dietary and environmental liver stressors, helping to counteract potential hepatotoxins. Furthermore, the formulation encourages the repair and renewal of healthy liver tissue, promoting hepatocyte regeneration. By stabilizing liver cell membranes, it strengthens the structural integrity of these cells, enhancing their resilience against damage. Additionally, the syrup exhibits significant antioxidant activity, scavenging harmful free radicals generated during the body's natural toxin metabolism, thereby preventing oxidative damage to the liver's delicate cellular structures.

Stimulates Healthy Appetite and Improves Digestive Function
A sluggish liver directly impacts digestive efficiency, often leading to appetite loss, bloating, and dyspepsia. LIV.52 Syrup addresses this core issue comprehensively. It enhances the secretion of digestive enzymes and bile, which are crucial for the proper breakdown of dietary fats and proteins. By improving overall gastrointestinal function, it reduces feelings of post-meal heaviness, bloating, and discomfort. Most notably, the formulation naturally helps stimulate the appetite center in the brain, encouraging a genuine desire for wholesome, nutritious food. This makes it an excellent choice for individuals with poor dietary intake, convalescing patients needing nutritional support for recovery, and children who are often categorized as "picky eaters," helping to ensure they receive the calories and nutrients necessary for their development.

Promotes Healthy Growth and Optimal Nutrient Utilization
This benefit is particularly significant for growing children, adolescents, and anyone seeking to improve their nutritional status. By optimizing core liver function, LIV.52 Syrup ensures efficient nutrient metabolism, meaning the proteins, vitamins, and minerals essential for development and cellular repair are processed effectively. It also enhances the bioavailability of nutrients from the food we consume, ensuring that the body can absorb and use a greater proportion of these vital compounds. By resolving underlying digestive and metabolic inefficiencies, it supports a healthy growth trajectory and weight gain that is directly correlated with an improved overall nutritional status, making it a valuable adjunct to a balanced diet.

Supports Overall Vitality and Holistic Well-being
The advantages of a well-supported liver extend far beyond the organ itself, creating a positive ripple effect throughout the entire body. Users often report increased energy levels as their metabolism becomes more efficient and nutrient utilization improves. The skin, which acts as a secondary detoxification organ, frequently shows a healthier, clearer appearance as the internal toxin load is managed more effectively by a robust liver. Furthermore, because the liver plays a pivotal role in immune function and systemic inflammation, supporting its health contributes to a strengthened overall immune response, helping the body maintain its natural defenses.

A Legacy of Trust: The Science and Ingredients Behind the Formula
Himalaya's commitment is embodied in its promise of "Wellness in Every Bottle, Health in Every Leaf." LIV.52 is not merely an ancient recipe; it stands as one of the most extensively researched herbal hepatoprotective formulations globally. Its reputation is built on a foundation of over 300 scientific studies and clinical trials investigating its efficacy, coupled with more than 65 years of trusted therapeutic use across international markets. This research substantiates its role in supporting liver function under various conditions and its proven ability to promote healthy appetite.

The efficacy of LIV.52 Syrup stems from the precise synergy of time-honored Ayurvedic botanicals. Key ingredients include Himroh (Capparis spinosa), a potent hepatoprotective agent known for its antioxidant and anti-inflammatory properties; Kasani (Cichorium intybus), which stimulates bile secretion, acting as a digestive bitter tonic and liver detoxifier; and Kasamarda (Cassia occidentalis), which supports liver function and exhibits strong antioxidant activity. The formula is rounded out by Arkapushpi (Cyanopsis tetragonoloba) for its nutritive and digestive properties, Biranjasipha (Achillea millefolium) for digestive health and appetite, and Jhavuka (Tamarix gallica) along with Mandur Bhasma (Processed Iron Oxide), which work synergistically to support healthy hemoglobin levels and overall metabolism, addressing the fatigue often associated with suboptimal liver health.

Ideal for a Wide Range of Individuals
LIV.52 Syrup is beneficial for adults and children experiencing low appetite or sluggish digestion. It serves as an excellent daily support for individuals seeking to fortify their liver due to lifestyle or dietary factors, those living in polluted urban environments, or people with occupational exposure to toxins. It is highly recommended for convalescing patients who need nutritional support and improved appetite to aid recovery. For growing children and adolescents, it provides foundational support for optimal nutrient absorption and development. Ultimately, it is a perfect choice for any health-conscious individual looking for a natural, well-researched detoxification and vitality aid.

Usage Guidelines for Optimal Results
For the best outcomes, it is recommended to take LIV.52 Syrup 30 minutes before meals to maximize its appetite-stimulating and digestive preparatory effects. The typical adult dosage is 2 teaspoonfuls (10ml) twice daily, while for children, the dosage is often 1 teaspoonful (5ml) twice daily. However, it is imperative to consult the package insert or a healthcare practitioner for precise dosage instructions tailored to individual needs. For general wellness and appetite promotion, a course of 4 to 8 weeks is commonly recommended. The syrup can also be used periodically as a detox support regimen.

Uncompromising Safety, Quality, and Commitment
Himalaya LIV.52 Syrup is crafted with the highest standards of purity and potency. It is a 100% natural, plant-based formulation containing no synthetic colors, flavors, or harmful preservatives. Every ingredient undergoes stringent quality control in a process that spans from seed to shelf, ensuring each bottle delivers consistent, scientifically validated efficacy. The formula is well-tolerated and safe for long-term use when taken as directed. It is presented in a convenient 100ml bottle complete with a graduated measuring cup for precise and easy dosing.

Addressing Common Questions

Is LIV.52 Syrup safe for children?
Yes, it is a safe and gentle formulation specifically suitable for children. Always adhere to the recommended pediatric dosage provided on the packaging or by a healthcare provider.

Can it be taken alongside other medications?
While it is a natural product, it is always prudent to consult your healthcare provider before starting any new supplement, especially if you are on prescription medications, to ensure there are no potential interactions.

How is the syrup different from LIV.52 tablets?
The core herbal formulation is similar. The syrup form is often preferred for children, those with swallowing difficulties, or for individuals seeking faster absorption. It also represents the traditional Ayurvedic liquid medium known as Asava-Arishta.

Are there any side effects?
LIV.52 Syrup is generally very well-tolerated when taken as directed. In rare instances, individuals with specific sensitivities to certain herbs may experience mild gastrointestinal effects.

Is it suitable for diabetics?
The standard syrup contains sugar as a preservative and palatability agent. Individuals with diabetes should consult their doctor before use and may consider the sugar-free LIV.52 DS tablet variant as an alternative.

Your Next Step Towards Holistic Liver Health
Do not let persistent fatigue, poor appetite, or the silent burden of modern toxins diminish your quality of life. Choose proactive, natural care rooted in both tradition and scientific validation. Choose Himalaya LIV.52 Syrup—a dedicated guardian of liver health trusted by generations. Invest in your body's essential detoxification center and experience the renewed vitality that comes with a well-supported, efficiently functioning liver. Make the commitment to your holistic well-being today by ordering your 100ml bottle of Himalaya LIV.52 Syrup.



HUMALOG® KwikPen® 100 units/mL: Precision, Convenience, and Confidence in Diabetes Management

For millions living with diabetes, insulin therapy is a cornerstone of daily life—a vital tool for maintaining glycemic control, preventing complications, and pursuing an active, fulfilling lifestyle. The challenge has always been to pair the life-saving efficacy of insulin with a delivery system that fits seamlessly into the rhythms of modern living. The HUMALOG® KwikPen®, pre-filled with 100 units/mL of rapid-acting insulin lispro, represents a significant evolution in this journey. More than just an insulin pen, it is an integrated solution designed to empower patients with unprecedented convenience, accuracy, and ease of use. This comprehensive description explores the features, benefits, and patient-centric design that make the HUMALOG KwikPen a trusted choice for diabetes management.

Advanced Insulin Action: The Science of HUMALOG (Insulin Lispro)

HUMALOG (insulin lispro) is a rapid-acting human insulin analog. Its molecular structure is engineered to be absorbed quickly and predictably from subcutaneous tissue. Compared to regular human insulin, HUMALOG has a more rapid onset (within 15 minutes), an earlier peak (approximately 1 hour), and a shorter duration (3 to 4 hours). This pharmacological profile allows for:

  • Meal-Time Flexibility: It can be taken immediately before (within 15 minutes) or immediately after a meal, accommodating unpredictable eating schedules.

  • Mimicking Physiological Response: It more closely mimics the body's natural prandial insulin spike, helping to control the sharp post-meal rise in blood glucose.

  • Reduced Hypoglycemia Risk: The shorter duration can lower the risk of late post-meal hypoglycemia.

The KwikPen delivers this advanced insulin in a ready-to-use, disposable format, eliminating the need for vial and syringe handling.

Unmatched Design: The KwikPen Advantage

The "Kwik" in KwikPen is a promise delivered through thoughtful engineering. Every aspect of its design is intended to simplify the injection process, reduce anxiety, and promote adherence.

  1. Pre-filled, Pre-measured Convenience: Each pen comes pre-filled with 3 mL of HUMALOG insulin lispro 100 units/mL, providing up to 300 units in a single device. This eliminates the steps of drawing insulin from a vial, ensuring sterility and removing a significant source of dosing error. It's ready to use straight from the refrigerator—simply attach a new pen needle, prime, and dose.

  2. Simple, Intuitive Dosing: The large, easy-to-grip dial and clear, digital dose window make dose setting straightforward, even for users with visual or dexterity challenges. The dose selector clicks audibly for each unit, providing tactile and auditory confirmation. The two-tone clicker is a standout feature: it produces a different sound when dialing up versus down, providing an extra layer of safety to prevent accidental over-dosing.

  3. Effortless Injection: The patented KwikInject™ mechanism requires low injection force. A gentle press with the thumb on the end of the pen is all that's needed to deliver the dose smoothly and comfortably. This is particularly beneficial for children, the elderly, or those with reduced hand strength.

  4. Discreet and Portable: With its sleek, compact design, the KwikPen easily fits into a purse, pocket, or dedicated carrying case. Its discreet appearance allows for confident dosing at work, in restaurants, or while traveling, supporting a lifestyle free from unnecessary interruptions.

  5. Robust Safety Features: The pen includes multiple safeguards:

    • Dose Safety Ring: A colored ring appears in the dose window to confirm a dose has been set.

    • Anti-Reverse Dial: Prevents the user from dialing beyond the remaining insulin, ensuring dose accuracy.

    • End-of-Dose Click: A distinct click signals when the full dose has been delivered.

The Complete System: Inclusion of Pen Needles

Recognizing that the injection experience depends on both the pen and the needle, this offering often includes compatible pen needles. Using a new, sterile needle with each injection is critical for:

  • Optimal Comfort: Sharp, thin-gauge needles (e.g., 32G 4mm or 31G 8mm are common) minimize pain and tissue trauma.

  • Dose Accuracy: A fresh needle ensures an unobstructed flow and precise insulin delivery. Reusing needles can cause clogging, corrosion, and dose inaccuracy.

  • Infection Prevention: A single-use, sterile needle drastically reduces the risk of skin infections and lipohypertrophy (lumpy tissue from repeated injections in the same spot).

Patients should consult their healthcare provider to select the ideal needle length and gauge for their body type and injection technique.

Clinical Benefits and Patient Outcomes

The integration of HUMALOG insulin with the KwikPen delivery system translates into tangible clinical and quality-of-life benefits:

  • Improved Glycemic Control: The convenience and accuracy of the system support better adherence to prescribed insulin regimens, a key factor in achieving target A1c levels.

  • Enhanced Adherence: By reducing the complexity and perceived burden of injections, patients are more likely to stick to their therapy, especially when multiple daily injections are required.

  • Increased Confidence: The foolproof design and clear feedback mechanisms empower patients, including those new to insulin, to self-administer with confidence.

  • Greater Freedom and Flexibility: The rapid action of HUMALOG and the portability of the KwikPen allow patients to manage their diabetes proactively without being tethered to a strict schedule or bulky equipment.

Ideal For a Broad Range of Patients

The HUMALOG KwikPen system is suitable for many individuals with diabetes who require rapid-acting insulin, including:

  • Adults and children with Type 1 Diabetes: For mealtime bolus dosing, often in conjunction with a long-acting basal insulin.

  • Adults with Type 2 Diabetes: To control postprandial glucose spikes when oral medications or non-insulin injectables are insufficient.

  • Newly diagnosed patients: Its ease of use can help ease the transition to insulin therapy.

  • Active individuals and frequent travelers: Its durability (in-use for up to 28 days at room temperature) and portability are major assets.

Important Safety Information

HUMALOG is indicated to improve glycemic control in adults and children with diabetes mellitus. Potential side effects include hypoglycemia (low blood sugar), hypokalemia (low blood potassium), allergic reactions, injection site reactions, lipodystrophy, itching, and rash. Hypoglycemia is the most common adverse effect. Do not use during episodes of hypoglycemia or if allergic to insulin lispro or any excipients. Do not share pens or needles between patients, even with a new needle, due to risk of bloodborne pathogen transmission.

Always consult a healthcare provider to determine if HUMALOG KwikPen is right for you, for proper dosing instructions, and for comprehensive training on injection technique, site rotation, and hypoglycemia management. The pen is for single-patient use only and should never be used with a syringe.

Conclusion: A Partnership in Care

The HUMALOG® 100 units/mL KwikPen is more than a medical device; it is a partner in daily diabetes management. By uniting the rapid, predictable action of insulin lispro with a pen designed for simplicity, accuracy, and dignity, it addresses the practical realities of living with diabetes. It transforms a complex medical task into a quick, manageable routine, allowing patients to focus less on the mechanics of their condition and more on living their lives to the fullest. For healthcare providers and patients seeking a reliable, user-friendly, and effective insulin delivery system, the HUMALOG KwikPen stands as a benchmark of innovation and patient-centered design.



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