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Bacteriostatic Water 30mL – Sterile, Multi-Dose Diluent for Pharmaceutical and Research Use | GenLabs

Product Code: [Insert Product Code]
Brand: GenLabs
Volume: 30mL Sterile Glass Vial
Preservative: 0.9% Benzyl Alcohol
pH: Balanced to 5.7 (approximately)
Sterility: Sterile Filtered (0.22 micron)
Certifications: cGMP Compliant Manufacturing
Packaging: Sealed, Tamper-Evident Vial with Color-Coded Flip-Off Cap

Introduction: The Gold Standard in Pharmaceutical Reconstitution

In the precise worlds of peptide research, hormone therapy, veterinary medicine, and advanced compounding, the integrity of your active compounds is paramount. However, even the most potent and pure substance is only as reliable as the diluent used to prepare it. Introducing GenLabs Bacteriostatic Water 30mL—the purpose-engineered, sterile solution designed for safe, multi-dose reconstitution and dilution of injectable medications and research peptides.

Bacteriostatic Water is not merely "sterile water." It is a sophisticated pharmaceutical vehicle, meticulously formulated with 0.9% Benzyl Alcohol. This critical additive inhibits microbial growth, allowing a single vial to be used safely for multiple doses over a defined period (typically 28 days), reducing waste and enhancing convenience without compromising sterility. GenLabs manufactures this essential tool under strict cGMP (Current Good Manufacturing Practice) conditions, ensuring every 30mL vial meets uncompromising standards of purity, clarity, and performance. For professionals and informed users who demand precision, this product is the foundational cornerstone of safe and effective solution preparation.

Detailed Product Features & Specifications

1. Pharmaceutical-Grade Sterility and Purity:
The cornerstone of the GenLabs formula is its guaranteed sterility. Each batch is filtered through a 0.22-micron microbiological filter, the industry standard for removing bacteria and potential endotoxins. The water itself is of the highest USP-grade purity, free from pyrogens and particulate contaminants. This ensures that the introduction of the diluent does not introduce any adulterants that could skew research results, cause adverse reactions, or degrade the stability of your reconstituted product.

2. 0.9% Benzyl Alcohol as a Bacteriostatic Agent:
The defining component of bacteriostatic water is the inclusion of Benzyl Alcohol at a concentration of 0.9%. This agent is not an antibacterial in the therapeutic sense but a highly effective bacteriostat. It functions by creating an environment that inhibits the proliferation of most microorganisms that may be inadvertently introduced during a multi-dose withdrawal procedure. This allows for the repeated, aseptic use of the vial for up to 28 days after initial puncture, provided it is stored correctly. It is crucial to note that this formulation is intended for multi-dose use only with compounds that are compatible with Benzyl Alcohol.

3. Optimized pH Balance for Compound Stability:
GenLabs Bacteriostatic Water is carefully adjusted to a slightly acidic pH of approximately 5.7. This is not arbitrary; this pH range is specifically chosen to maximize the stability and solubility of a wide array of peptides and hormonal compounds. A neutral or alkaline pH could lead to accelerated degradation or precipitation of sensitive molecules. Our balanced formula helps maintain the molecular integrity of your reconstituted product from the first dose to the last.

4. Secure, Contamination-Resistant Packaging:
Each 30mL of solution is housed in a sterile, Type I borosilicate glass vial. This pharmaceutical-grade glass is non-reactive, prevents leaching, and ensures the solution remains uncontaminated by the container. The vial is sealed with a sterile bromobutyl rubber stopper, chosen for its superior resealing properties after needle puncture. The entire assembly is secured with an aluminum crimp seal and a distinctive, color-coded flip-off plastic cap, providing a clear, tamper-evident guarantee to the end-user.

5. cGMP Compliance & Traceability:
GenLabs products are manufactured in facilities that adhere to cGMP guidelines. This represents a commitment to quality control far beyond basic standards. It encompasses rigorous documentation, environmental monitoring, raw material testing, and final product release assays. This level of scrutiny provides assurance that every vial is part of a traceable, quality-assured production process.

Primary Applications and Uses

GenLabs Bacteriostatic Water 30mL is an indispensable diluent across multiple fields:

• Peptide Research: The preferred solvent for reconstituting lyophilized (freeze-dried) research peptides for in vitro or laboratory animal studies. Its bacteriostatic property is essential for multi-dose experimental protocols.

• Compounding Pharmacy: Used by licensed pharmacists to compound customized injectable medications, including hormone replacement therapies (e.g., testosterone, hCG), pain management solutions, and other sterile preparations.

• Veterinary Medicine: Employed in veterinary practices for reconstituting vaccines, antibiotics, and hormones for administration to animals.

• Professional and Educational Settings: Used in laboratory training, medical education, and other settings requiring a reliable, multi-dose sterile diluent for practice or specific procedures.

Important Note: This product is a diluent/solvent only. It contains no active pharmaceutical ingredient (API). It must be used by or under the supervision of qualified individuals who understand sterile technique and the properties of the compound being reconstituted.

Usage Guidelines & Storage Instructions

Proper Reconstitution Technique:

1. Aseptic Hand Hygiene: Begin by thoroughly washing hands and working in a clean, draft-free environment.

2. Sanitize Surfaces: Wipe the rubber stopper of both the Bacteriostatic Water vial and the target compound vial with a fresh 70% isopropyl alcohol swab.

3. Equalize Pressure: Draw a volume of air into your sterile syringe equal to the amount of bacteriostatic water you intend to withdraw. Inject this air into the Bacteriostatic Water vial.

4. Withdraw Diluent: Invert the vial, withdraw the desired volume of water slowly and carefully.

5. Reconstitute: Gently inject the water down the side of the target vial containing the lyophilized powder. Avoid directly spraying onto the powder cake. Swirl gently or roll between hands until the solution is completely clear and the powder is fully dissolved. Do not shake vigorously, as this can cause denaturation of fragile proteins/peptides.

Storage: Store the sealed vial at controlled room temperature (20°-25°C or 68°-77°F), protected from light and freezing. After initial puncture, the vial can be stored for up to 28 days. Always inspect the solution visually before each use; it must be clear, colorless, and free of any particles or cloudiness. Discard if contamination is suspected or after the 28-day window.

Why Choose GenLabs Bacteriostatic Water 30mL?

• Uncompromised Safety: The 0.9% Benzyl Alcohol formula is the USP-standard for safe multi-dose use, providing a critical defense against microbial contamination.

• Guaranteed Purity: cGMP manufacturing and 0.22-micron filtration deliver a sterile, pyrogen-free product you can trust.

• Enhanced Stability: The optimized pH helps preserve the potency and solubility of your valuable reconstituted compounds.

• Professional-Grade Packaging: Tamper-evident, sterile glass vial with a resealing rubber stopper ensures product integrity from our facility to your point of use.

• Cost-Effective Convenience: The 30mL multi-dose format minimizes waste, making it an economical and practical choice for ongoing research or treatment protocols.

Frequently Asked Questions (FAQ)

Q: Can this be used for single-dose injections?
A: While it can be, single-dose injections typically require Sterile Water for Injection (SWFI), which contains no preservative. Bacteriostatic Water is specifically designed for multi-dose applications.

Q: Is this safe for human injection?
A: As a sterile, USP-grade pharmaceutical diluent, it is formulated for injection once mixed with a compatible compound. It is NOT for direct intravenous injection as a standalone product. Always follow the guidance of a licensed healthcare provider.

Q: What is the shelf life of an unopened vial?
A: Refer to the expiration date printed on the vial. When stored properly in its sealed condition, it typically has a shelf life of 18-24 months from the date of manufacture.

Q: Why is there a 28-day limit after opening?
A: The bacteriostatic effectiveness of the 0.9% Benzyl Alcohol, combined with the risk of incremental contamination through repeated needle entries, dictates this standard pharmaceutical safety window. Adhering to it is critical.

Q: Is it suitable for all peptides and compounds?
A: Most, but not all. Always verify the compatibility of your specific compound with Benzyl Alcohol. Some specific peptides or individuals with sensitivities may require alternative diluents like Sterile Water for Injection or Sodium Chloride (Bacteriostatic) 0.9%.

Conclusion: The Essential Component for Precision

Reconstitution is the first and most critical step in activating a lyophilized compound. Choosing an inferior diluent risks contamination, instability, and inaccurate dosing. GenLabs Bacteriostatic Water 30mL eliminates this variable, providing a reliable, professionally trusted foundation for your work.

Whether you are advancing a research hypothesis, compounding a tailored medication, or managing veterinary care, ensure your process begins with the gold standard in sterile dilution.

Order GenLabs Bacteriostatic Water 30mL today—where precision meets purity.

Disclaimer: This product is intended for laboratory research, pharmaceutical compounding, and professional use only. It is not for direct human or animal use without being properly compounded with an active ingredient by a qualified professional. The user assumes all responsibility for the safe and appropriate handling and application of this product. Always consult with a healthcare professional or qualified expert for specific guidance.

IGF-1 LR3 (Long R3 IGF-1) – 1mg/vial – Premium Research Peptide Solution

Product Identifier: IGF-1 LR3 (Long R3 IGF-1)
Concentration: 1 milligram (1 mg) per sterile lyophilized vial
Inclusion: 1 vial of Bacteriostatic Water (0.9% Benzyl Alcohol) for reconstitution
Manufacturer: GenLabs
Application: For research use only. Not for human or veterinary consumption.

Introduction: Unlocking the Next Frontier in Growth Factor Research

In the intricate world of cellular communication and tissue regeneration, Insulin-like Growth Factor-1 (IGF-1) stands as a pivotal mediator. GenLabs is proud to introduce its high-fidelity research-grade IGF-1 LR3 (Long R3 IGF-1), a meticulously engineered and significantly more potent analog of native IGF-1. Presented as a 1mg lyophilized powder alongside a complimentary vial of Bacteriostatic Water, this offering is designed for the exacting demands of advanced in vitro research. Our product represents a cornerstone for scientists and research institutions exploring the frontiers of cell proliferation, differentiation, repair mechanisms, and metabolic pathways.

What is IGF-1 LR3 (Long R3 IGF-1)?

IGF-1 LR3 is a recombinant 83-amino acid polypeptide, a modified version of the 70-amino acid native human IGF-1. The "LR3" denotes two critical modifications:

1. Substitution of Arginine for Glutamic Acid at position 3: This minor change subtly alters the molecule's interaction profile.

2. A 13-amino acid extension peptide at the N-terminus: This is the defining "Long R3" feature.

These deliberate modifications are not arbitrary; they are engineered to confer distinct advantages over the native form for research purposes, primarily by dramatically reducing its binding affinity for IGF-binding proteins (IGFBPs) in serum.

Mechanism of Action & Key Research Advantages

Native IGF-1 is rapidly bound and inactivated by a family of IGFBPs in biological fluids, which can limit its bioavailability and activity in experimental settings. The GenLabs IGF-1 LR3 variant is specifically designed to circumvent this limitation.

• Enhanced Bioavailability & Prolonged Activity: The extended peptide chain and amino acid substitution significantly impair binding to most IGFBPs. This results in a research compound with vastly increased half-life and bioavailability in cell culture media and other research systems. Consequently, IGF-1 LR3 exhibits more potent and sustained activity, allowing researchers to observe effects with greater clarity and over extended observation periods.

• Potent Mitogenic & Anabolic Signaling: Like native IGF-1, IGF-1 LR3 exerts its effects by binding to and activating the IGF-1 receptor (IGF-1R), a transmembrane tyrosine kinase receptor. This activation triggers two primary intracellular signaling cascades:

  1. The MAPK/ERK Pathway: Primarily responsible for stimulating cellular proliferation (mitogenesis) and differentiation.

  2. The PI3K/AKT/mTOR Pathway: Primarily responsible for promoting protein synthesis, glucose uptake, and inhibiting apoptosis (cell death), leading to hypertrophic and anabolic outcomes.

• Research Applications: Due to its enhanced stability and potency, IGF-1 LR3 is an invaluable tool for investigating:

  • Myoblast & Skeletal Muscle Studies: Examining satellite cell activation, differentiation into myotubes, and muscle protein synthesis.

  • Chondrocyte & Osteoblast Research: Exploring cartilage formation, bone growth, and repair mechanisms.

  • Neurotrophic Effects: Studying neuronal survival, axonal growth, and potential protective mechanisms.

  • Fibroblast & Connective Tissue Research: Investigating collagen synthesis, skin repair, and wound healing models.

  • Metabolic Studies: Analyzing glucose metabolism and cellular nutrient uptake.

  • General Cell Culture: Promoting the health and proliferation of various difficult-to-culture cell lines.

Why Choose GenLabs IGF-1 LR3?

1. Uncompromising Purity & Quality Assurance: Every batch of GenLabs IGF-1 LR3 is synthesized using state-of-the-art solid-phase peptide synthesis (SPPS) and undergoes rigorous purification via HPLC (High-Performance Liquid Chromatography). Each vial is accompanied by independent third-party laboratory analysis (COA) verifying peptide content, purity (typically >98%), and sterility.

2. Precise 1mg Dosage Format: The standardized 1mg per vial allows for accurate, reproducible dosing and simplifies calculation for your specific research protocols, ensuring consistency across experiments.

3. Included Bacteriostatic Water: We provide a sterile vial of Bacteriostatic Water (0.9% Benzyl Alcohol) with each peptide. This ready-to-use solvent ensures proper reconstitution while inhibiting bacterial growth in the multidose solution post-reconstitution, maintaining sterility for the duration of your research.

4. Sterile, Lyophilized Presentation: The peptide is provided as a sterile, lyophilized (freeze-dried) white powder in a sealed glass vial. This format guarantees stability during transport and long-term storage, protecting the integrity of the molecule.

5. Commitment to Research Integrity: GenLabs products are manufactured, packaged, and sold explicitly for laboratory research purposes. We serve only qualified research entities and do not condone or support unauthorized use.

Handling, Reconstitution & Storage Protocol

Storage (Unreconstituted): Store the lyophilized peptide and Bacteriostatic Water at -20°C or below upon receipt. For long-term storage (over 6 months), -80°C is recommended. Keep the product in its original container, protected from light.

Reconstitution:

1. Aseptic Technique: Perform all steps in a sterile laminar flow hood using sterile instruments.

2. Slow Introduction of Solvent: Gently inject the Bacteriostatic Water down the side of the peptide vial, avoiding forceful direct stream onto the powder.

3. Gentle Reconstitution: Swirl the vial slowly or roll it between your hands until the powder is fully dissolved. Do not shake vigorously, as this can denature the peptide.

4. Concentration Calculation: The final concentration depends on the amount of Bacteriostatic Water used. For a standard 1mg vial, adding 1mL yields a concentration of 1000mcg/mL. Adding 2mL yields 500mcg/mL, etc.

Storage (Reconstituted): Once reconstituted with the provided Bacteriostatic Water, the solution should be stored refrigerated at 2-8°C and used within a timeframe appropriate for sterile, preservative-containing solutions (typically up to 30 days when handled aseptically). For extended usability, aliquoting and freezing at -20°C or -80°C is advised. Avoid repeated freeze-thaw cycles.

Important Disclaimer & Safety Information

• Intended Use: This product is labeled and sold FOR LABORATORY RESEARCH USE ONLY. It is not intended for diagnostic, therapeutic, or human consumption purposes.

• Handling: The product should be handled only by qualified, trained researchers in appropriately equipped laboratory settings. Personal protective equipment (PPE) including gloves, lab coat, and eye protection must be worn.

• Compliance: Purchasers are responsible for ensuring their compliance with all local, state, federal, and institutional regulations regarding the acquisition, storage, and use of research peptides.

Conclusion: A Definitive Research Tool

GenLabs' IGF-1 LR3 – 1mg/vial represents the synthesis of cutting-edge peptide engineering and stringent quality control. Its enhanced potency, prolonged activity, and superior bioavailability make it an indispensable reagent for pioneering research into growth, repair, and metabolic processes at the cellular level. By providing this high-purity compound alongside the necessary reconstitution solution, GenLabs empowers the scientific community to conduct reliable, reproducible, and groundbreaking research with confidence.

Trenbolone Acetate 100mg is a powerful anabolic steroid that is widely used in the bodybuilding and athletic communities. It belongs to the class of drugs known as androgenic anabolic steroids (AAS) and is derived from the hormone testosterone.

Trenbolone Acetate is highly regarded for its potent anabolic properties, making it a popular choice among athletes and bodybuilders looking to enhance their performance and build muscle mass. It is renowned for its ability to promote rapid gains in strength and muscle size, making it a favorite among those seeking to achieve significant improvements in their physique.

One of the primary reasons for its popularity is its exceptional ability to increase nitrogen retention in the muscles. Nitrogen retention is vital for muscle growth, and by increasing it, Trenbolone Acetate creates an optimal environment for muscle tissue development. This leads to enhanced protein synthesis and greater muscle hypertrophy, resulting in a more muscular and well-defined physique.

Additionally, Trenbolone Acetate is known to increase red blood cell production, leading to improved oxygenation and endurance. This allows athletes to train harder and longer, thereby maximizing their performance during intense workouts or competitions.

Furthermore, this steroid has a high affinity for androgen receptors, which means it binds strongly to these receptors in the body. This results in increased fat burning and a reduction in body fat percentage, giving users a more chiseled and shredded appearance.

However, it is important to note that Trenbolone Acetate 100mg is a potent steroid with a high potential for side effects. Some of the common side effects associated with its use include androgenic effects such as acne, oily skin, and increased facial and body hair. It may also suppress natural testosterone production, leading to hormonal imbalances and potential reproductive issues.

Due to its potency, Trenbolone Acetate 100mg should be used with caution and under the guidance of a healthcare professional. It is typically administered via intramuscular injection and is commonly cycled for a duration of 8-12 weeks.

In conclusion, Trenbolone Acetate 100mg is a powerful anabolic steroid that offers significant benefits in terms of muscle growth, strength gains, and fat loss. However, it should be used responsibly and with proper knowledge of its potential side effects. Consultation with a healthcare professional is recommended before starting any steroid cycle to ensure safety and optimal results.

Methenolone enanthate, also known as Primobolan Depot, is an anabolic androgenic steroid (AAS) that is derived from dihydrotestosterone (DHT). It is classified as a mild steroid due to its low androgenic properties, making it popular among athletes and bodybuilders who seek lean muscle gains with minimal side effects.

Methenolone enanthate is available in injectable form, with the enanthate ester attached to the hormone, which allows for a slow and steady release in the body. This esterification process extends the half-life of the steroid, resulting in a longer duration of action.

When it comes to its anabolic effects, methenolone enanthate promotes protein synthesis and nitrogen retention, leading to muscle growth and improved recovery. It is often used during cutting cycles to preserve lean muscle mass while reducing body fat. Due to its mild nature, it is less likely to cause water retention or estrogenic side effects such as gynecomastia.

One of the key benefits of methenolone enanthate is its ability to increase strength without adding excessive muscle mass. This makes it an ideal choice for athletes who compete in weight-class sports or those who want to enhance their performance without gaining significant bulk.

Another advantage of methenolone enanthate is its low potential for androgenic side effects. This means that users are less likely to experience acne, oily skin, hair loss, or aggression often associated with more potent androgenic steroids.

However, it is important to note that methenolone enanthate is a relatively weak steroid compared to some others on the market. Consequently, significant muscle gains may require higher dosages, which can increase the risk of adverse effects.

Like any steroid, methenolone enanthate carries potential side effects, although they tend to be milder compared to stronger AAS. These can include suppression of natural testosterone production, cholesterol imbalances, liver toxicity (when used orally), and cardiovascular strain. Post-cycle therapy (PCT) is recommended to help restore hormonal balance and minimize the risk of side effects.

It is crucial to mention that the use of methenolone enanthate, like any other AAS, should be done under the supervision of a qualified healthcare professional. They can provide guidance on dosages, cycle length, and any necessary support to ensure safety and maximize benefits.

In conclusion, methenolone enanthate is a mild AAS that offers lean muscle gains, increased strength, and improved recovery. It is a popular choice for athletes and bodybuilders seeking moderate effects with a lower risk of androgenic side effects. However, it is essential to approach its use with caution, follow proper dosage guidelines, and prioritize overall health and well-being.

GHK-Cu (glycyl-histidyl-lysine-copper) is a peptide that consists of three amino acids: glycine, histidine, and lysine, along with a copper ion. This peptide is derived from a larger protein called copper-binding protein, which is naturally present in our bodies.

GHK-Cu has gained significant attention in the field of skincare and anti-aging due to its potential benefits. It has been found to have several biological activities that make it appealing for its potential use in skincare products.

1. Skin rejuvenation: GHK-Cu has been shown to promote collagen production, which helps to improve skin elasticity and firmness. Collagen is a crucial protein responsible for maintaining the structure and strength of the skin. By stimulating collagen synthesis, GHK-Cu may help to reduce the appearance of fine lines and wrinkles, making the skin look more youthful.

2. Wound healing: GHK-Cu has been extensively studied for its wound healing properties. It has been shown to accelerate the healing process by promoting the migration of cells involved in tissue repair, such as fibroblasts and keratinocytes. Additionally, it has anti-inflammatory effects that can help to reduce inflammation and redness associated with wounds.

3. Antioxidant activity: GHK-Cu has antioxidant properties, meaning it can help protect the skin from damage caused by free radicals. Free radicals are unstable molecules that can damage cells and contribute to the aging process. By neutralizing free radicals, GHK-Cu may help to prevent oxidative stress and maintain a healthier skin appearance.

4. Anti-inflammatory effects: GHK-Cu has been found to have anti-inflammatory properties, which can help to soothe and calm the skin. It can reduce the production of pro-inflammatory molecules and inhibit the activation of inflammatory pathways. This makes it beneficial for individuals with skin conditions such as acne, rosacea, or dermatitis.

GHK-Cu is available in various forms, including creams, serums, and gels, for topical application. It is essential to note that GHK-Cu is a potent peptide and should be used as directed by professionals or according to product instructions. It is advisable to consult a dermatologist or healthcare provider before incorporating GHK-Cu into your skincare routine, especially if you have any underlying skin conditions or are taking medication.

Overall, GHK-Cu peptide shows promise in promoting skin rejuvenation, wound healing, antioxidant protection, and anti-inflammatory effects. It is important to stay updated with scientific research and consult professionals for the most accurate and up-to-date information on its benefits and usage.

GLUTAMINE 500 MG – HI-TECH: The Cornerstone of Recovery and Resilient Health

In the relentless pursuit of peak physical performance, the true differentiator isn’t just the intensity of your training—it’s the quality of your recovery. Every rep, sprint, and lift creates microscopic stress, demanding precise nutritional tools to repair, rebuild, and return stronger. Hi-Tech Pharmaceuticals introduces GLUTAMINE 500 mg, a premium, pharmaceutical-grade formulation designed to be that essential tool. More than just a muscle supplement, this high-potency L-Glutamine is engineered to address the trifecta of an athlete’s well-being: accelerated muscular recovery, enhanced immune defense, and foundational gut health.

Glutamine, the most abundant conditionally essential amino acid in the human body, is a critical fuel source for immune cells and the intestinal lining. During periods of intense physical stress, metabolic demand for glutamine can far exceed the body’s production, creating a deficit that can hinder progress, compromise immunity, and prolong fatigue. Hi-Tech Glutamine 500 mg provides a concentrated, pure source to replenish these vital stores, ensuring your body operates from a position of strength, not scarcity.

The Science of Glutamine: Beyond Muscle Recovery

While revered for its role in protein synthesis, glutamine’s functions are profoundly systemic.

• Muscle Protein Synthesis & Anti-Catabolism: Post-exercise, glutamine levels plummet. Supplementation helps shift the body from a catabolic (breaking down) state to an anabolic (building up) state. It supports the synthesis of new muscle proteins while helping to reduce muscle breakdown, particularly during high-volume or calorie-restricted phases.

• Immune System Fortification: Lymphocytes, macrophages, and other immune cells utilize glutamine as a primary fuel source, especially during times of stress. Adequate glutamine levels are crucial for maintaining a robust immune response, helping you stay consistent in your training by supporting your body’s natural defenses.

• Gut Integrity & Nutrient Absorption: The cells of the small intestine (enterocytes) use glutamine as their preferred energy source. This supports the maintenance of a strong, healthy gut lining—a critical barrier against pathogens and toxins. A healthy gut is fundamental not only for digestion and nutrient absorption but also for overall systemic inflammation control and immune function, a concept known as "gut-mediated immunity."

• Glycogen Replenishment: Glutamine plays a role in gluconeogenesis, the process of generating glucose from non-carbohydrate sources. This can aid in the restoration of muscle glycogen stores, your muscles' primary energy reservoir, paving the way for renewed energy and performance in subsequent workouts.

Why Choose Hi-Tech Pharmaceuticals Glutamine 500 mg?

In a market saturated with under-dosed and impure supplements, Hi-Tech stands apart with an uncompromising commitment to quality, potency, and transparency.

• Pharmaceutical-Grade Purity: Each capsule contains precisely 500 mg of pure, micronized L-Glutamine. No proprietary blends, no fillers, no unnecessary additives. You are investing in the exact nutrient your body requires.

• Optimal Serving Size & Flexibility: The 500 mg per capsule format offers unparalleled dosing flexibility. Tailor your intake precisely to your body weight, training intensity, and specific goals—whether that's 2 grams daily for general wellness or 10+ grams for targeted post-training and gut health support.

• Manufactured in cGMP-Certified Facilities: Hi-Tech products are produced in state-of-the-art facilities that adhere to the rigorous Current Good Manufacturing Practices (cGMP) enforced by the FDA. This guarantees every bottle meets the highest standards of identity, purity, strength, and composition.

• The Hi-Tech Legacy: Backed by decades of scientific research and a reputation for producing effective, high-quality supplements, Hi-Tech Pharmaceuticals is a name trusted by athletes, bodybuilders, and health-conscious individuals worldwide.

Who Can Benefit from Hi-Tech Glutamine 500 mg?

• Strength & Endurance Athletes: For those engaged in weight training, HIIT, cross-training, or endurance sports, glutamine is non-negotiable for mitigating exercise-induced muscle soreness (DOMS) and speeding the repair process.

• Fitness Enthusiasts in Caloric Deficits: When dieting or cutting, the body is at a higher risk of muscle loss. Glutamine’s anti-catabolic properties help preserve hard-earned lean muscle mass.

• Individuals Focused on Gut Health: Those managing gut permeability, digestive discomfort, or seeking to strengthen their overall gut microbiome will find glutamine an essential, research-backed supplement.

• Anyone Undergoing Physical Stress: From demanding work schedules to illness, glutamine demand increases. Supplementation can help maintain immune competence and metabolic balance.

Suggested Use & Integration into Your Regimen

For general wellness and gut support: Take 2-4 capsules (1-2 grams) daily, between meals or on an empty stomach.
For active recovery and athletic performance: Take 4-10 capsules (2-5 grams) immediately following exercise, and consider an additional 2-4 capsules before bed to leverage the body’s nocturnal repair cycles.
For targeted gut health protocols: Consult with a healthcare professional. Doses are often spread throughout the day, typically on an empty stomach.

Glutamine pairs synergistically with other staples in your supplement regimen. Combine with BCAAs or Essential Amino Acids (EAAs) intra-workout for a comprehensive anti-catabolic and recovery boost. Post-workout, take with your protein shake and carbohydrates to create a powerful anabolic environment for muscle repair and glycogen replenishment.

Frequently Asked Questions (FAQ)

Q: Is L-Glutamine safe?
A: L-Glutamine is generally recognized as safe (GRAS) when used as directed. It is a naturally occurring amino acid found abundantly in many whole food sources like meat, eggs, and dairy.

Q: Can I take too much glutamine?
A: While the body efficiently utilizes glutamine, extremely high doses (above 20-30 grams per day) may cause minor gastrointestinal upset in some individuals. It is always advisable to start with a standard dose and assess tolerance.

Q: Should I take glutamine on rest days?
A: Absolutely. Recovery is a 24/7 process. Supplementing on rest days helps maintain elevated plasma glutamine levels, continuously supporting immune function, gut integrity, and the ongoing repair of muscle tissue.

Q: How is this different from glutamine peptides?
A: Hi-Tech Glutamine 500 mg is pure, free-form L-Glutamine. It requires no further digestion and is rapidly absorbed into the bloodstream. Glutamine peptides are bound to other peptides; some argue they have different absorption rates, but free-form glutamine remains the gold standard for purity and proven efficacy.

Invest in Your Foundation

Your body is a complex system where performance, health, and recovery are inextricably linked. Neglecting one pillar weakens the entire structure. Hi-Tech Glutamine 500 mg is more than a single-purpose supplement; it is a foundational nutrient designed to fortify your body’s core systems from within.

Choose GLUTAMINE 500 MG – HI-TECH. Choose comprehensive recovery, resilient health, and the confidence that comes from fueling your ambition with pharmaceutical-grade precision.

Introduction: Reclaim Comfort from Acute Muscular Pain

Acute musculoskeletal pain—whether from a sudden back strain, a painful muscle spasm, or a post-injury recovery period—can be debilitating. It disrupts sleep, limits mobility, and impacts overall quality of life. In such scenarios, rest and targeted therapy are crucial. PAIN-O-SOMA 500mg, manufactured under the stringent quality standards of HAB Pharma, is a centrally-acting prescription muscle relaxant designed as an adjunct to rest, physical therapy, and other measures for the short-term relief of acute, painful musculoskeletal conditions. This detailed guide will explore its mechanism, proper use, safety profile, and essential considerations for patients.

Understanding PAIN-O-SOMA (Carisoprodol): Mechanism of Action

PAIN-O-SOMA contains the active ingredient Carisoprodol 500mg. It is classified as a musculoskeletal relaxant that works centrally (in the brain and spinal cord), not directly on the muscles themselves. Its precise mechanism, while not fully understood, is believed to involve:

• Modulation of Nerve Communication: Carisoprodol is thought to interrupt neuronal communication within the reticular formation and spinal cord, areas critical for transmitting pain signals and maintaining muscle tone.

• Sedative Effects: It produces mild sedative effects, which can help alleviate the discomfort and anxiety associated with acute pain, allowing the patient to rest and engage in prescribed therapies.

• Metabolism to Meprobamate: Importantly, Carisoprodol is metabolized in the liver to meprobamate, a compound with known anxiolytic and sedative properties. This metabolite contributes to the overall therapeutic effect.

It is vital to understand that PAIN-O-SOMA is not a painkiller (analgesic) in the traditional sense. It does not block pain at the site of injury like an NSAID (e.g., Ibuprofen). Instead, it helps break the cycle of pain-muscle spasm-pain by reducing the sensation of muscle tightness and spasm, thereby facilitating recovery.

Indications: When is PAIN-O-SOMA 500mg Prescribed?

PAIN-O-SOMA is indicated for the short-term relief (typically 2-3 weeks) of acute, painful musculoskeletal conditions. It is always used as part of a comprehensive treatment plan. Common scenarios include:

• Acute Lower Back Pain: Particularly pain associated with muscle spasms and stiffness.

• Muscle Strains and Sprains: Resulting from sports injuries, accidents, or overexertion.

• Musculoligamentous Injuries: Pain related to injuries affecting muscles and supporting ligaments.

• Fibromyalgia & Other Conditions: As an adjunctive therapy, as determined by a healthcare provider.

Important: PAIN-O-SOMA is not intended for chronic pain management or for use in children under 16 years of age.

Dosage and Administration: A Precise Regimen for Safety

Dosage: The usual adult dosage of PAIN-O-SOMA is one 500mg tablet taken three times daily and at bedtime. The bedtime dose is crucial for relieving nighttime muscle spasms that can disrupt sleep.

Duration: Therapy should be limited to two to three weeks due to the lack of evidence of long-term efficacy and the potential for dependence (see warnings).

Administration: Tablets should be swallowed whole with a full glass of water. They can be taken with or without food, though taking with food may minimize potential stomach upset.

Critical Instructions:

• Strictly Prescription-Based: This is a Schedule IV controlled substance. Use only as prescribed by a qualified physician.

• Do Not Exceed Dosage: Never increase the dose or frequency without medical consultation.

• Adjunct Therapy: PAIN-O-SOMA works best when combined with rest, physical therapy, heat/cold application, and other interventions your doctor recommends.

Warnings, Precautions, and Contraindications: Safety First

1. Dependence and Abuse Potential:
Carisoprodol has a known potential for psychological and physical dependence, abuse, and withdrawal. This risk is heightened in patients with a history of substance abuse (alcohol, opioids, benzodiazepines) or psychiatric disorders. Abrupt discontinuation after prolonged use can lead to withdrawal symptoms like anxiety, insomnia, nausea, and, in severe cases, seizures. Use must be short-term and under strict medical supervision.

2. Sedation and Impairment:
PAIN-O-SOMA may cause significant drowsiness, dizziness, and impaired cognitive and motor skills. Patients must be cautioned:

• Do not drive, operate machinery, or perform hazardous tasks while using this medication.

• Avoid alcohol completely. Alcohol potentiates sedation and dangerously impairs judgment and coordination.

• Use caution with other CNS depressants (e.g., opioids, benzodiazepines, certain antidepressants).

3. Seizures:
There is a risk of seizures, both during use and in the withdrawal period. This risk is higher in patients with seizure disorders or those taking other medications that lower the seizure threshold.

4. Hypersensitivity Reactions:
Rare but serious reactions have been reported, including angioedema (facial swelling), anaphylaxis, and severe skin reactions (e.g., Stevens-Johnson syndrome, toxic epidermal necrolysis). Discontinue immediately at the first sign of rash, itching, swelling, or difficulty breathing and seek emergency medical attention.

5. Specific Patient Contraindications:

• Porphyria: Carisoprodol is contraindicated in patients with acute intermittent porphyria.

• Allergy: To carisoprodol, meprobamate, or any tablet excipients.

• Severe Hepatic/Kidney Impairment: Use with extreme caution or avoid, as metabolism and excretion may be impaired.

• Pregnancy and Lactation: Not recommended unless absolutely necessary and benefits outweigh risks. Consult your doctor.

Side Effects: What to Expect and Monitor

Common side effects are often dose-related and may include:

• Drowsiness, dizziness, lightheadedness

• Headache

• Tachycardia (fast heart rate)

• Postural hypotension (low blood pressure upon standing)

• Nausea, vomiting, upset stomach

Less common but serious side effects requiring medical attention: Severe rash, itching, swelling (face/tongue/throat), difficulty breathing, fever, weakness, loss of coordination, confusion, severe dizziness, mood changes, vision problems.

Drug Interactions: A Critical Discussion with Your Doctor

Inform your doctor about all medications you take, including:

• CNS Depressants: Opioids (hydrocodone, oxycodone), benzodiazepines (alprazolam), sleep aids, antipsychotics—increased risk of profound sedation, respiratory depression, coma, or death.

• Enzyme Inducers/Inhibitors: Medications affecting liver enzymes (e.g., CYP2C19 inducers like rifampin or inhibitors like fluvoxamine/omeprazole) can alter carisoprodol levels.

• Other Muscle Relaxants: Potential additive effects.

Why Choose HAB Pharma’s PAIN-O-SOMA 500mg?

HAB Pharma is a reputable pharmaceutical manufacturer committed to Good Manufacturing Practices (GMP). PAIN-O-SOMA offers:

• Standardized Potency: Ensures each 500mg tablet delivers consistent therapeutic effect.

• Quality Assurance: Manufactured in facilities adhering to rigorous quality control standards.

• Clear Packaging: The 10-tablet foil pack ensures product integrity, protects from moisture, and aids in adherence to short-term treatment protocols.

Conclusion: A Short-Term Tool for a Specific Purpose

PAIN-O-SOMA 500mg is a potent and effective medication for breaking the cycle of acute muscle spasm and pain. Its role is specific and time-limited. Success and safety hinge on a transparent partnership between patient and prescriber. Honesty about medical history, adherence to the prescribed short-term regimen, vigilance for side effects, and integration with non-pharmacological therapies are the cornerstones of effective treatment.

Introduction: A Balanced Approach to Mealtime and Basal Insulin Needs

For individuals with diabetes managing postprandial (after-meal) blood glucose spikes alongside overall daytime control, finding an insulin regimen that is both effective and convenient is paramount. The HUMALOG MIX50 KWIKPEN, manufactured by the trusted global leader Eli Lilly and Company, offers a scientifically engineered, premixed solution. It combines the rapid onset of insulin lispro with the sustained action of its protamine-crystallized counterpart in a precise 50/50 ratio. This product description provides a comprehensive overview of this unique insulin analog, its clinical benefits, the innovative KwikPen delivery system, and essential guidelines for use, empowering patients and caregivers with the knowledge for informed diabetes management.

What is Humalog Mix50? Understanding the Dual-Phase Action

Humalog Mix50 is a sterile, white suspension containing a dual-phase mixture of two distinct insulin analogs:

• 50% Insulin Lispro Protamine Suspension: This component acts as an intermediate-acting insulin. The protamine binding delays absorption, providing a steady release of insulin lispro over a prolonged period (typically up to 12-24 hours), covering basal insulin needs and controlling blood sugar between meals.

• 50% Insulin Lispro Injection: This component is a rapid-acting insulin. It is identical to natural human insulin but with a reversed sequence of two amino acids, allowing it to be absorbed into the bloodstream much faster. It begins working within approximately 15 minutes after injection, peaking in about 30 minutes to 2.5 hours, to effectively manage the sharp rise in blood glucose following a meal.

This premixed formulation is designed to simplify regimens for patients who require both mealtime and basal coverage, reducing the number of daily injections while addressing two critical aspects of glycemic control.

Key Clinical Benefits and Advantages

1. Simplified Regimen: By combining two insulin actions in one pen, Humalog Mix50 reduces injection frequency compared to separate basal and bolus injections, potentially improving adherence to prescribed therapy.

2. Targeted Postprandial Control: The high proportion (50%) of rapid-acting insulin lispro makes it particularly effective at controlling the significant blood glucose elevations that occur after meals, a key contributor to overall HbA1c levels.

3. Predictable Intermediate Coverage: The 50% intermediate-acting component provides a reliable baseline of insulin activity, helping to maintain stable glucose levels between meals and overnight when dosed appropriately.

4. Proven Efficacy: As part of the Humalog family, the insulin lispro component has a long-standing clinical history of effective glucose-lowering with a reduced risk of hypoglycemia compared to regular human insulin, especially post-meal.

The Humalog KwikPen: Engineered for Ease, Accuracy, and Discretion

The medication is delivered via the state-of-the-art Humalog KwikPen, a testament to patient-centric design:

• Simple, Accurate Dosing: Features a large, easy-to-read dose window and a distinct click sound for each unit dialed, minimizing dosing errors. The dial-down mechanism allows for precise dose selection from 1 to 60 units in 1-unit increments.

• Ease of Use: The pen requires no vial or syringe handling. It is pre-filled and primed with a few simple steps. Its ergonomic, non-slip shape is comfortable to hold, even for users with dexterity challenges.

• Convenient and Portable: The compact, durable design is ideal for an active lifestyle. It can be easily carried in a bag or pocket for discreet dosing at home, work, or while dining out.

• Safety-First Design: Includes safety features like a rubberized grip and a built-in clip. Requires compatible pen needles (sold separately), which must be attached before each use and discarded afterward.

Indications and Usage

Humalog Mix50 KwikPen is indicated to improve glycemic control in adults and pediatric patients with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus. It is typically prescribed for patients who require a premixed insulin product to manage both prandial and basal glucose levels. The specific dosing regimen (often twice daily before major meals) must be meticulously determined by a healthcare provider based on individual metabolic needs, blood glucose monitoring patterns, and lifestyle factors.

Administration Guidelines

• Route: For subcutaneous injection only. Never administer intravenously or intramuscularly.

• Injection Sites: Rotate injection sites within the same region (abdomen, thigh, upper arm, or buttock) to reduce the risk of lipodystrophy. Absorption rates vary slightly by site.

• Timing: Administer within 15 minutes before a meal due to the rapid-acting component. Consistency in timing relative to meals is crucial.

• Preparation: The suspension must be mixed thoroughly before each injection. Gently roll the pen between your palms 10 times and invert it 10 times until the fluid appears uniformly cloudy or milky. Do not shake vigorously.

• Needles: Always use a new, sterile pen needle for each injection to ensure sterility, prevent needle blockage, and ensure a sharp, less painful injection. Safely discard the needle after each use.

Important Safety Information & Potential Side Effects

• Hypoglycemia: The most common and potentially serious adverse effect. Symptoms include sweating, dizziness, tremor, palpitations, hunger, and confusion. Patients must be educated on recognition, treatment (fast-acting carbohydrates), and prevention through regular glucose monitoring and consistent meal patterns.

• Hypersensitivity & Allergic Reactions: Severe, life-threatening allergic reactions are possible. Localized reactions (redness, swelling, itching at the injection site) may occur.

• Weight Gain: Can occur with insulin therapy due to the anabolic effects of improved glycemic control.

• Hypokalemia: Insulin causes a shift of potassium into cells, which may lower blood potassium levels.

• Lipodystrophy: Can occur at injection sites if rotation is not practiced.

• Contraindications: During episodes of hypoglycemia and in patients hypersensitive to insulin lispro or any excipients.

WARNING: RISK OF MEDICATION ERRORS: Humalog Mix50 is one of several premixed ratios (including Mix75/25 and Mix50/50). Always verify the exact product name and ratio (50/50) before dispensing and administering to avoid errors, which could lead to serious hypoglycemia or hyperglycemia.

Storage Instructions

• Unused Pens (Refrigerated): Store at 2°C to 8°C (36°F to 46°F). Do not freeze. Keep away from the cooling element.

• In-Use Pen: Once a pen is in use, it may be kept at room temperature (below 30°C / 86°F) for up to 28 days. Do not refrigerate the pen you are currently using. Always store with the pen cap on to protect from light.

• Do Not Use if the solution appears clear, contains particles, or is discolored.

Conclusion: A Trusted Tool for Integrated Diabetes Management

The HUMALOG MIX50 KWIKPEN represents a fusion of advanced pharmaceutical science and thoughtful device engineering. It offers a valuable therapeutic option for patients who benefit from the simplicity and efficacy of a premixed insulin with a higher proportion of rapid-acting analog. When used as part of a comprehensive diabetes management plan—including regular blood glucose monitoring, medical nutrition therapy, physical activity, and ongoing healthcare provider supervision—it can be a powerful tool in achieving and maintaining target glycemic goals, reducing the risk of long-term complications, and enhancing quality of life.

Disclaimer: This information is for educational purposes only and does not constitute medical advice. Individual treatment plans must be developed by a qualified healthcare professional. Patients should always consult their doctor or diabetes educator for guidance on insulin initiation, dosing, administration, and management of side effects.