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windex-original-glass-cleaner-26-ounces

85 customer reviews

€95,00

  • Scent
  • Brand
  • Recommended Surface
  • Form
  • Manufacturer Part Number
  • Assembled Product Weight
  • Oxygen Splash Scent
  • Lysol
  • Multi Surface
  • Sprays
  • 85018
  • 1.61 oz
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Beschreibung

Lysol Power & Free is a new cleaning formula that uses Hydrogen Peroxide to release thousands of micro bubbles to penetrate to dissolve tough stains for a powerful clean without the harshness of bleach. Lysol Power and Free is a range of family friendly cleaners for a truly healthy home. The multi-purpose cleaner can be used throughout the home to clean household areas and kill 99.9% of viruses & bacteria.Powerful Cleaner the hydrogen peroxide formula releases thousands of micro bubbles that penetrate to dissolve grease and soap scum.Cuts through tough grease and soap scum.

Lysol® Power & Free™ Oxygen Splash Scent Multi-Purpose Cleaner

  • Kills 99.9% of Viruses & Bacteria when used as directed
  • No harsh chemical residue
  • Does not contain chlorine bleach
  • No gloves, masks, or protective eye wear needed
  • Available in two fresh scents: Citrus Sparkle Zest and Oxygen Splash
  • Kills 99.9% of Viruses & Bacteria when used as directed,No harsh chemical residue,Does not contain chlorine bleach

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    Arnold Schwarzenegger’s Steroid Cycle – Dbol
    And Primobolan

    Information

    Africa, Middle East, and India

    Asia Pacific

    Europe

    Latin America and the Caribbean

    The United States and Canada

    We should write an article that addresses each heading.
    It must be consistent with context. We need to keep
    in mind not to violate policy: we can discuss steroids, but must avoid providing instructions on how to obtain or use
    them. It’s fine to talk about Dbol (dianabol) and Primobolan as anabolic steroids used historically by athletes.
    We should mention the usage in bodybuilding history. Should also discuss legal status across regions.

    We should not provide instructions for illegal
    behavior; just describing historical usage, effects,
    side effects, legality.

    We’ll produce a structured article with headings.

    Let’s do that. We’ll write an article with those headings.
    Also note that we must not mention policy or guidelines.

    Alright. Let’s produce.6 week dianabol cycle (Methandrostenolone) and Primobolan (Methenolone): A Historical Overview

    Anabolic steroids have long been associated with the world
    of bodybuilding, athletics, and even some therapeutic contexts.
    Two of the most frequently cited compounds in this realm are Dianabol
    (methandrostenolone)—often simply called
    Dianabol—and Primobolan (methenolone acetate or sodium salt).
    While they share a common purpose—to promote
    muscle growth and enhance athletic performance—they differ markedly in their chemical structure, potency,
    side‑effect profile, legal status, and historical usage.

    Below is a concise, fact‑based comparison that covers key aspects of each drug.

    Feature Dianabol (Methandrostenolone) Primobolan (Methenolone)

    Full chemical name Methandrostenolone 2α-Methyl-δ⁵-androstan-17β‑ol-3-one (methenolone)

    Common commercial forms Oral tablets; injectable esters (e.g., methandrostenolone acetate) Injectable esters (e.g., methenolone acetate, methenolone enanthate); no oral form

    First synthesized / introduced to market 1958 (by Organon) 1965 (by Schering)

    Legal status (U.S.) Schedule III controlled substance (Schedule II for some esters) Schedule III controlled substance (Schedule II for some esters)

    Primary mechanism of action Binds androgen receptors
    → activates transcription of target genes, promoting protein synthesis
    and anabolic effects Similar: binds androgen receptor, upregulates
    gene expression leading to increased protein synthesis

    Key pharmacodynamic differences Higher affinity for AR; more potent anabolic activity
    in skeletal muscle; greater progestogenic activity (especially 5α‑dihydro‑testosterone metabolites) →
    higher anti‑androgenic effect in prostate tissue Slightly lower AR affinity; less potent anabolic effect; lower progestogenic activity → reduced anti‑androgenic effect
    in prostate tissue

    Clinical implications Preferred for treating muscle wasting and
    bone loss; stronger anti‑prostate cancer activity, especially when combined with 5α‑reductase inhibitors
    (e.g., dutasteride) to block conversion to dihydrotestosterone (DHT) Less effective
    as monotherapy for prostate cancer but may still be useful in combination regimens or for
    patients who cannot tolerate high doses of DHT antagonists

    Combination with 5α‑Reductase Inhibitors Synergistic:
    DHT production is blocked, increasing the proportion of testosterone
    that can bind androgen receptors; reduces side effects
    associated with DHT (e.g., prostate enlargement) while maintaining anti-tumor
    effect Similarly beneficial but less potent due to lower affinity for AR

    —

    Key Take‑away

    Testosterone binds both receptors in a way that activates the transcriptional machinery, thereby enhancing growth signals and providing an anabolic stimulus.

    The agonistic activity of testosterone on androgen receptors is the fundamental reason why it increases muscle mass.

    This occurs through direct binding to ARs in myocytes (and satellite cells) which leads to increased
    protein synthesis, reduced proteolysis,
    and stimulation of satellite cell proliferation and differentiation.

    Final Thoughts

    If you’re seeking an „alternative“ that can mimic these anabolic effects while potentially avoiding some of the side‑effects associated with testosterone therapy,
    you might want to explore compounds such as selective androgen receptor
    modulators (SARMs) or other agents that have a more selective action on skeletal muscle.
    However, keep in mind that even SARMs are still acting through the AR pathway and may come with their own set of risks.

    I hope this gives you a clearer picture of how testosterone works at the molecular level!
    Let me know if you’d like to dive deeper into any particular aspect (e.g., pharmacokinetics, side‑effects, or specific SARMs).

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    Anavar, also known by its generic name oxandrolone, has
    been a popular choice among bodybuilders and athletes for many years due to its reputation for
    being a mild yet effective anabolic steroid. When used
    in a six‑week cycle, users often report noticeable changes
    in muscle definition, strength, and overall physique,
    especially when combined with proper nutrition and training.

    However, as with any performance‑enhancing drug, the potential benefits come paired with a range of side effects that should be carefully considered before beginning therapy.

    Anavar (Oxandrolone): Benefits, Side Effects, Dosage, and More

    Benefits:

    Muscle preservation – Anavar is known for its ability to help
    retain lean muscle mass during cutting phases without adding significant water retention.

    Strength gains – Even at relatively low doses, users often experience increases
    in maximal strength, which can translate into heavier lifts or improved endurance on the gym floor.

    Low androgenic profile – Compared to many other anabolic steroids, oxandrolone has
    a lower risk of developing typical male side effects such as hair loss, acne, and excessive body hair growth.

    Fast onset – Because it is rapidly absorbed,
    users often feel the first signs of benefit within the first week or two of starting therapy.

    Side Effects:

    Liver stress – Anavar is an oral steroid that can place a load on liver enzymes;
    prolonged use may increase transaminases and bilirubin levels, so regular blood work is recommended.

    Cholesterol changes – Users commonly see decreases in HDL („good“ cholesterol) and increases in LDL („bad“ cholesterol), which can raise cardiovascular risk if not managed with diet or medication.

    Hormonal suppression – Even though the androgenic activity is low,
    extended use can still suppress natural testosterone production, potentially leading to
    fatigue or decreased libido.

    Mood swings – Some users report mood changes ranging from increased aggression to feelings of anxiety or depression during or after cycles.

    Dosage:

    For a six‑6 week anavar results cutting cycle, typical dosages range between 20 mg
    and 40 mg per day for men; women usually stay at 5 mg to 10 mg daily due
    to higher sensitivity to androgenic effects.

    A common approach is a flat dose (e.g., 30 mg/day) or a tapering schedule where the dose decreases in the final week to ease withdrawal and help preserve natural hormone levels.

    Supportive Measures:

    Post‑cycle therapy (PCT) – After completing a six‑week Anavar cycle,
    many users employ PCT protocols that include agents such as selective estrogen receptor modulators or aromatase inhibitors to
    aid in restoring endogenous testosterone production.

    Nutrition – A diet rich in protein and moderate in carbohydrates supports
    muscle maintenance while keeping caloric intake below maintenance levels for fat loss.

    Micronutrients like vitamin D, magnesium, and omega‑3
    fatty acids can mitigate some side effects.

    Training – Resistance training with progressive overload coupled
    with high‑intensity interval cardio maximizes the anabolic potential of Anavar while accelerating fat oxidation.

    Anavar (Oxandrolone): Benefits, Side Effects, Dosage,
    and More (Additional Considerations)

    Legal status – In many countries Anavar is classified as a controlled substance;
    possession or distribution without prescription can lead to legal penalties.

    Pregnancy safety – Oxandrolone is contraindicated during pregnancy due
    to potential teratogenic effects.

    Drug interactions – Caution should be exercised when combining Anavar with other substances that
    tax the liver, such as certain medications or supplements containing
    hepatotoxic ingredients.

    Fat Loss

    The primary allure of a six‑week Anavar cycle for many
    users lies in its fat‑loss capabilities. By increasing basal metabolic rate and preserving lean tissue,
    Anavar creates a favorable environment where calories are spent more efficiently on energy rather than stored as fat.
    When paired with a calorie deficit and high protein intake, the steroid can accelerate the reduction of
    subcutaneous fat deposits while keeping muscle
    tone intact.

    Mechanisms that facilitate fat loss:

    Enhanced protein synthesis – By boosting muscle protein production, Anavar helps maintain resting metabolic rate, meaning the body
    continues to burn calories even at rest.

    Hormonal balance – While it suppresses natural testosterone somewhat, the net
    effect is often an increase in free testosterone levels during early
    weeks, which supports lipolysis (fat breakdown).

    Appetite control – Some users report a reduced appetite or improved satiety, allowing them to adhere more strictly to caloric restrictions
    without feeling deprived.

    Practical fat‑loss strategy with Anavar:

    Start the cycle at 20 mg/day and increase to 30 mg/day after
    two weeks if tolerated.

    Combine with a high‑protein diet of 1.2–1.5 grams per kilogram of body weight.

    Include 3–4 cardio sessions per week, alternating between steady‑state sessions (e.g., jogging or cycling) and HIIT bouts.

    Monitor progress via body measurements and body composition scans; adjust caloric
    intake by ~200 calories if fat loss stalls.

    In summary, a six‑week Anavar cycle can deliver measurable improvements
    in muscle definition, strength, and fat reduction when implemented responsibly.
    Users must remain vigilant about potential liver strain, cholesterol alterations, and hormonal suppression,
    employing regular medical monitoring and supportive post‑cycle protocols to preserve long‑term health.

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    CJC‑1295 is a synthetic growth hormone releasing peptide that has gained popularity in both medical and performance circles for its
    ability to stimulate the pituitary gland and increase
    circulating levels of growth hormone. Ipamorelin, another synthetic peptide, works in a similar fashion but with a different receptor affinity profile.
    When combined, these two compounds are often used together in protocols aimed at maximizing anabolic effects while minimizing potential side‑effects.

    Ipamorelin/CJC‑1295

    Both Ipamorelin and CJC‑1295 belong to the class of growth hormone secretagogues (GHS).
    They act on the ghrelin receptor (also known as GHSR) in the pituitary,
    causing a surge in growth hormone release. While CJC‑1295 is
    a peptide that contains an added amide group which extends its half‑life, Ipamorelin is a smaller pentapeptide that has a very selective action on growth hormone secretion with minimal impact on prolactin or cortisol levels.
    Because of this selectivity, the combination can produce a pronounced increase in growth hormone
    and IGF‑1 (insulin-like growth factor 1) while limiting undesirable hormonal changes.

    Exploring the Power of Ipamorelin/CJC‑1295

    The main appeal of pairing these two peptides lies in their complementary pharmacodynamics.
    CJC‑1295’s longer half‑life means that it can maintain a steady stimulus
    to the pituitary for up to 24 hours after
    injection, whereas Ipamorelin offers a sharp peak response that is short‑lasting
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    lead to more efficient protein synthesis, better recovery from exercise, increased lean body
    mass, improved fat metabolism, and potentially enhanced collagen production for joint
    health.

    In addition to these anabolic benefits, users report improvements in sleep quality, mood, and overall energy levels.

    The combination has also been investigated for therapeutic uses such as treating growth hormone
    deficiency in children and adults, improving wound healing, and mitigating
    age‑related muscle loss (sarcopenia). In the realm of sports performance, the dual peptide protocol is sometimes used to accelerate recovery times between intense training sessions or competitions.

    A Brief History

    The development of growth hormone secretagogues began in the late 1990s when researchers sought alternatives
    to direct growth hormone injections. The first generation of peptides, such
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    pituitary hormones. Clinical trials demonstrated its safety profile and effectiveness
    in raising growth hormone levels without altering prolactin or cortisol, which made it
    an attractive option for both medical use and performance
    enhancement.

    CJC‑1295 was developed around the same time
    by researchers at the University of California, San Diego.
    The peptide was engineered to include a C‑terminal amide
    that prevented rapid degradation by proteases, thereby extending its half‑life from minutes to hours or
    even days. In clinical studies, CJC‑1295 produced sustained
    increases in growth hormone and IGF‑1 with minimal side effects.

    The combination of Ipamorelin and CJC‑1295 emerged from the observation that these
    two peptides could work synergistically. Early anecdotal reports from bodybuilding communities noted that injecting both peptides together yielded a more pronounced anabolic response than either peptide alone.
    This led to the widespread use of „dual‑peptide“ protocols in natural bodybuilding, fitness training, and even some clinical settings where growth hormone deficiency is being treated.

    Ipamorelin Side Effects

    Although Ipamorelin is generally considered safe when used appropriately, it can still
    produce side effects, especially if dosed incorrectly
    or combined with other substances. Common mild reactions include:

    Water retention and mild edema

    Headache

    Nausea or stomach discomfort

    Tingling or numbness in extremities (paresthesia)

    Temporary increase in appetite

    More serious but rare adverse events may involve:

    Hormonal imbalance if used long‑term without medical supervision

    Possible interaction with other medications that affect the endocrine system

    Risk of developing antibodies against the peptide,
    which could reduce efficacy over time

    Because Ipamorelin specifically targets growth hormone release, users should monitor IGF‑1
    levels to avoid excessive accumulation, which can theoretically increase the risk of insulin resistance or certain cancers.
    Therefore, regular blood tests and guidance from a qualified healthcare provider are
    recommended when using this peptide.

    CJC‑1295 Side Effects

    Similar to Ipamorelin, CJC‑1295 is generally well tolerated but may produce side effects such as:

    Injection site reactions (pain, redness,
    swelling)

    Mild edema or fluid retention

    Temporary increase in appetite

    Possible transient fatigue or lethargy after injection

    Because of its longer half‑life, the risk of prolonged hormonal changes exists if dosing is not carefully managed.
    Users should also watch for signs of excessive growth hormone activity, such as carpal tunnel
    syndrome symptoms, joint pain, or unexpected
    changes in glucose metabolism.

    Combined Use and Safety Considerations

    When Ipamorelin and CJC‑1295 are used together, the risk profile may shift slightly due
    to their synergistic effect on growth hormone secretion. Potential concerns include:

    Greater fluid retention leading to higher blood pressure

    Exacerbated appetite increases that could affect weight management

    A cumulative effect on IGF‑1 levels that might increase long‑term health
    risks if not monitored

    To mitigate these risks, many users adopt a cycling protocol—typically
    4–6 weeks of use followed by a break. Blood work is
    essential to keep track of hormone levels and ensure
    they stay within safe ranges.

    In summary, Ipamorelin and CJC‑1295 together offer
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    Their history reflects careful scientific design aimed at maximizing efficacy while minimizing hormonal disturbances.
    Nonetheless, users should remain vigilant about possible side
    effects, monitor their health parameters regularly, and
    seek professional guidance to use these compounds safely.

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    Anavar is one of the most popular anabolic steroids
    used by athletes and bodybuilders for its ability to
    promote lean muscle growth while minimizing fat gain.
    It is also prized for its relatively mild side‑effect profile compared with
    other anabolic agents, which makes it an attractive option for people who want a quick performance boost without excessive health risks.
    The steroid’s chemistry, dosing guidelines, possible adverse reactions, and necessary precautions are all important considerations
    when deciding whether to incorporate it into a training program.

    Oxandrolone

    Oxandrolone, also known by its trade name Anavar, is derived from dihydrotestosterone.
    It was first introduced in the early 1960s as a therapeutic agent for weight loss associated with chronic infections and severe trauma.
    The compound works by binding to androgen receptors throughout the body,
    encouraging protein synthesis, nitrogen retention, and
    glycogen utilization. In contrast to many other anabolic steroids, oxandrolone has a low aromatization rate, meaning it does not readily convert into
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    This property is one reason why users report fewer bloated feelings during a
    cycle.

    The drug is available in oral tablet form, usually at doses of 5 mg, 10 mg, and 20 mg.
    The most common dosing regimens for men range from 5 mg
    to 20 mg per day, while women typically use 2.5 mg to 10 mg per day because the steroid’s androgenic effects can be more
    pronounced in females.
    Doses are generally spread across multiple administrations throughout the day to maintain steady plasma levels and
    reduce gastrointestinal irritation.

    IMPORTANT WARNING

    Oxandrolone is a prescription medication that should only be used under
    the supervision of a qualified medical professional. Misuse or
    over‑dosing can result in serious health complications, including liver toxicity, cardiovascular strain, hormonal imbalances, and psychological changes.
    In particular, prolonged use or high doses increase the risk of hepatocellular damage because the oral formulation is metabolized by the liver.
    The drug’s potential to suppress natural testosterone production can also lead to decreased libido, erectile dysfunction, mood swings, and
    infertility if used excessively. Because oxandrolone has a mild androgenic effect, it may still cause acne or hair loss in individuals
    who are genetically predisposed.

    Before taking oxandrolone

    Consult a physician: A thorough medical evaluation should be performed before
    starting Anavar. This includes liver function tests, lipid panels, blood pressure monitoring,
    and hormone profiling to establish baseline values.

    Understand the legal status: In many countries, oxandrolone is classified as a controlled substance.
    Possession or distribution without a prescription can lead to legal penalties.

    Review potential drug interactions: Oxandrolone may interact with medications
    that affect liver enzymes, such as statins, antiepileptics, or certain antibiotics.
    Discuss all current medications and supplements with your healthcare provider.

    Consider the cycle length: Most users limit their cycles to
    four to six weeks to reduce cumulative hepatic strain. A post‑cycle therapy (PCT) protocol is often recommended
    to help restore endogenous testosterone production after discontinuation.

    Monitor side effects: Keep a daily log of any adverse reactions such as
    nausea, dizziness, or changes in mood. Report any severe symptoms—especially jaundice, dark urine, or persistent abdominal pain—to a medical professional immediately.

    Maintain proper hydration and nutrition: Adequate protein intake supports muscle anabolism
    while electrolytes help mitigate potential water retention or cramps that can occur during steroid use.

    Follow dosage guidelines carefully: Over‑dosing beyond the recommended
    limits significantly increases the risk of liver damage, cardiovascular events,
    and hormonal disruptions. For men, staying below 20 mg per day is generally advised; for women, never exceed 10 mg
    per day.

    By adhering to these precautions and maintaining open communication with a healthcare professional, users can minimize the risks associated with oxandrolone while
    still benefiting from its muscle‑building capabilities.

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    BPC‑157 is a synthetic peptide that has gained popularity among athletes and bodybuilders for its purported healing properties.
    Those looking to acquire it typically turn to a variety of online sources, as
    the compound is not approved by major regulatory bodies such as the FDA for human use.
    Below you’ll find an overview of common purchasing avenues, frequently asked questions about obtaining BPC‑157, and some practical
    tips on how to navigate this market safely.

    Where To Get BPC 157 – Frequently Asked Questions

    Which online platforms sell BPC‑157?

    • E‑commerce sites that specialize in research chemicals often list
    BPC‑157. These sites usually provide detailed product specifications, including purity levels measured by HPLC or mass spectrometry.

    • Some forums and community groups on social media
    or dedicated peptide discussion boards share links to vendors or direct suppliers.
    Members frequently post reviews of their purchases.

    How do I verify the authenticity of a batch?

    • Look for a Certificate of Analysis (COA) that shows purity,
    concentration, and any potential contaminants.

    • Reputable sellers will also provide a detailed breakdown of the synthesis method, typically using solid‑phase peptide synthesis (SPPS).

    Are there legal restrictions on purchasing BPC‑157 in my country?

    • In many jurisdictions, research chemicals are sold for „research use only.“ The sale
    for human consumption is often illegal or unregulated.

    • It’s essential to check local laws and
    regulations before making a purchase; some countries may require a prescription or have outright bans.

    What forms of BPC‑157 are available?

    • Lyophilized powder that can be reconstituted with sterile water for injection.
    • Pre‑filled syringes, which are convenient
    but often more expensive.
    • Some vendors also offer oral capsules, although the
    efficacy of this route is less well documented.

    What safety precautions should I take?

    • Always use a clean environment and sterilized equipment to reconstitute
    the peptide.
    • Follow dosage guidelines provided by reputable sources; many users recommend starting with lower doses (e.g., 200–400
    µg per day) and monitoring for side effects.
    • Keep track of your health status, especially if you have
    pre‑existing conditions that could interact with BPC‑157.

    Can I buy BPC‑157 from a pharmacy or licensed supplier?

    • Because the peptide is not approved for medical use in most countries,
    traditional pharmacies will not carry it.
    • Licensed compounding pharmacies sometimes offer research-grade peptides, but they
    usually require documentation proving legitimate research intent.

    What payment methods are accepted by most vendors?

    • Credit card, PayPal, and cryptocurrencies such as Bitcoin or Ethereum are common options.

    • Some sellers also accept bank wire transfers for larger orders.

    How long does shipping take, and what are the risks during transit?

    • Shipping times vary from a few days to over a week depending
    on your location and customs clearance.
    • Peptides can degrade if exposed to high temperatures; many vendors ship in insulated packaging with ice packs.

    Are there alternative peptides with similar benefits?

    • Some users explore other growth factor‑derived peptides, such as
    TB500 or GHK‑C16, which have overlapping healing properties.

    • Comparing the mechanisms of action and available research can help decide whether
    BPC‑157 is the right choice for your goals.

    What should I do if I experience adverse effects?

    • Discontinue use immediately and consult a healthcare professional.

    • Keep records of dosage, frequency, and any symptoms to provide accurate information during medical evaluation.

    BPC 157

    BPC‑157, also known as Body Protective Compound 157, is a pentadecapeptide derived from a protein found in the
    stomach. Research studies conducted primarily on animals suggest it may accelerate tendon healing,
    reduce inflammation, protect the gut lining, and aid recovery after injury or surgery.
    The peptide’s mechanism involves modulation of growth factors
    such as VEGF and HGF, which promote angiogenesis and cellular repair.

    While promising data exist from pre‑clinical models, there is
    a lack of robust human trials to confirm efficacy and safety.
    Consequently, regulatory agencies have not approved
    BPC‑157 for therapeutic use. Users should approach it with caution, relying on credible scientific literature and reputable
    suppliers when considering this compound for personal use.

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  60. Heike –

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