Cystone

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Cystone

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Cystone

Cystone is an Ayurvedic proprietary medicine classified as a polyherbal combination, utilizing a synergistic mixture of natural plant extracts and mineral compounds. The formulation is manufactured by The Himalaya Drug Company (Himalaya Wellness) and is widely distributed as an over-the-counter (OTC) product.

Property Description
Active Ingredients Polyherbal (Shilapushpa, Pasanabheda, Hajrul Yahood Bhasma)
Form Tablet (Uncoated), Syrup
Pharmacological Class Antilithiatic, Lithotriptic, Diuretic
Common Use Support for Urinary Tract Health
Origin Natural, Ayurvedic (India)

Cystone: What Type of Medicine Is It?

Cystone is primarily supplied for oral administration, typically as an uncoated tablet or a syrup suitable for a broad patient group. This classification as an Ayurvedic proprietary medicine roots its formulation in traditional Indian medical principles, adapted for contemporary commercial availability. Unlike single-molecule drugs, the characteristic of this natural combination is the synergistic activity of its plant constituents.


Composition and Pharmacological Classification

Cystone’s high-level pharmacological class is defined by its core actions: it is categorized as an antilithiatic and lithotriptic agent, alongside a diuretic effect. The formulation is a combination product that utilizes key botanical extracts, including Shilapushpa (Didymocarpus pedicellata) and Pasanabheda (Saxifraga ligulata). The formulation is intended to help reduce the supersaturation of calcium oxalate and other salts in the urine, which are primary factors in the development of urinary calculi. This multi-point approach is designed to assist in preventing mineral crystallization in the urinary pathways.


General Purpose for Urinary Tract Health

Cystone's overall purpose is to maintain and support healthy function within the urinary tract, particularly in managing conditions related to the buildup of mineral crystals. Its combined lithotriptic and diuretic actions help reduce the aggregation of crystals and promote increased urine flow, which aids in flushing small particles or gravel from the system. The polyherbal constituents of Cystone demonstrate anti-adherent properties, which help to prevent bacteria from adhering to the walls of the urinary tract. This provides general support in maintaining a clear and protected urinary environment.

What side effects are possible with Cystone?

Official Adverse Reactions and System-Organ Safety

The safety profile for Cystone, an Ayurvedic proprietary medicine, is derived from official regulatory documentation that generally classifies documented adverse effects as infrequent. The available safety data cites two primary categories of potential effects based on the body systems involved:

  • Immune System Disorders: Potential for allergic reactions.
  • Gastrointestinal Disorders: Potential for dyspeptic disorders (discomfort or pain in the upper abdomen).

No specific serious adverse reactions are explicitly documented or classified in the publicly available regulatory prescribing information for this product using the standardized MedDRA terminology for serious effects.

Safety Considerations for Specific Populations

Official regulatory documents define clear safety restrictions concerning specific patient populations, ensuring the safety profile is maintained:

  • Pediatric Population: Use of Cystone is officially contraindicated in children under 6 years of age.
  • Pregnancy and Lactation: Use during these sensitive periods requires a physician's prescription and assessment to ensure that the potential therapeutic benefit outweighs any potential risk.

Safety-Related Restrictions

Regulatory documentation also defines high-level constraints related to the medicine's application. Administration is not advisable in cases of threatening urethra obstruction caused by large crystalline aggregates or calculi. This constraint relates to the medicine's general support function for the urinary tract and is an important consideration in the overall safety assessment.

Overdose and Emergency Response

Overdose and When to Seek Help

The official regulatory profile for Cystone, an over-the-counter polyherbal medicine, does not include a detailed, formally documented toxicological syndrome. This absence of specific data in major regulatory monographs defines the official approach to potential over-ingestion.

Overdose Scope

Official government sources do not formally list specific clinical signs, symptoms, or laboratory abnormalities resulting from an acute over-ingestion of this formulation. Likewise, no specific dose levels or serious, life-threatening outcomes are explicitly stated in available regulatory documentation. The same lack of specific documentation applies to population-specific overdose notes regarding children, the elderly, or patients with hepatic or renal impairment.

Emergency Actions and Management

The universal regulatory requirement for any suspected acute intoxication is to seek immediate medical attention. Immediate contact with emergency services or a regional Poison Control Center is required if a significant amount is ingested beyond the recommended dosage.

As no specific antidote is documented for Cystone, official guidelines dictate that management should consist of symptomatic and supportive treatment. Furthermore, clinical monitoring and hospital observation are generally required to assess the patient’s condition following any over-ingestion event of an unknown nature.

Therapeutic Uses of Cystone

What Cystone Treats: Main Uses and Benefits

Cystone is an Ayurvedic polyherbal formulation that is commonly used to help with conditions characterized by periods of heightened symptoms related to the urinary system. The primary domain of use is relevant to addressing the discomfort associated with conditions involving urinary calculi (kidney stones) and crystalluria (crystals in the urine).

These types of formulations are used to address the symptomatic burden associated with urolithiasis. The product may assist with maintaining functional stability within the urinary system, contributing to easing the overall symptom load.

This is considered relevant for easing symptoms related to physical discomfort, such as painful or burning urination (dysuria), and symptoms that create noticeable physiological strain. It may be part of symptomatic management applied in clinical settings that involve acute or unstable symptom patterns. The formulation is applied across therapeutic domains that involve certain distressing symptoms associated with urinary conditions, including: symptoms associated with conditions involving recurrent or episodic manifestations, crystalluria, and discomfort during urination. The preparation assists with maintaining functional stability within the urinary system. The use is often seen during phases when symptoms become more noticeable, offering supportive relief when symptoms interfere with routine activities.


Quick Fact: Relevant for Symptoms Related to Physical Discomfort

Eligibility and Restrictions for Use

Who Can and Cannot Use Cystone?

The eligibility for Cystone use is defined by official regulatory documentation that specifies strict exclusions based on age, physiological status, and acute conditions. The product is primarily formulated for the adult population under standard labeled conditions.


Contraindications and Non-Eligibility

Population or Condition Regulatory Status
Hypersensitivity Contraindicated in individuals with a known allergy to any ingredient in the formulation.
Children Under 6 Years Contraindicated in this age group, as specified in certain regional regulatory summaries.
Acute Ureteral Obstruction Use is Not Advisable where large calculi cause acute or complete obstruction of the urinary tract.
Children Under 14 Years Not Recommended in some regional product information.

Conditional Use

Use during pregnancy and lactation is subject to strict regulatory conditions. Status varies by region, being either explicitly prohibited or allowed only as conditional use requiring a physician’s prescription. For the general adult population without the above restrictions or contraindications, the medicine may be used as labeled.

What should I know about interactions with other medicines?

Interactions with other medicines and products

This section outlines the officially documented interaction profile of Cystone, an Ayurvedic proprietary polyherbal formulation, as defined by government regulatory documents and approved prescribing information.


Interaction Scope

The regulatory profile of Cystone is currently characterized by the absence of officially documented interaction data. No specific medicinal products or substance classes are listed in official labels as having formal interaction patterns with Cystone.

Category Official Regulatory Status
Medicinal product categories with documented interactions None formally documented.
Mechanistic basis of interactions (e.g., CYP enzymes) None formally documented.
Timing-based interaction rules None formally documented. (No mandatory dose separation required)
Interaction-related restrictions None formally documented. (No prohibitions on co-administration)

Interaction Classifications (High-Level)

Category Official Regulatory Status
Interaction severity classification Undocumented. (No official severity assigned)
Interaction-context constraints None formally documented. (No official constraints regarding food, alcohol, or supplements)

Official Interaction Statements

Official regulatory documents and approved prescribing information for this formulation currently state that no clinically significant drug interactions have been reported with Cystone. The regulatory structure defines the product's interaction status by the lack of specific prohibitions, restrictions, or required adjustments concerning other medicines or products.

Mechanism of Action

Inhibition of Mineral Crystallization and Matrix Disruption

Cystone involves mechanisms that alter the chemical environment and dynamics of the urinary tract, utilizing the synergistic actions of its polyherbal components. The formulation directly interferes with the initial steps of crystal deposition and aggregation by reducing the supersaturation of mineral salts and inhibiting the nucleation and growth of crystals. A core action is the disruption and degradation of the organic mucin matrix, the biological scaffold that binds small crystals. This mechanism acts at the physicochemical level, resulting in the reduction of the structural integrity of mineral aggregates.

Spasmolysis and Enhanced Fluid Dynamics

Components exert a spasmolytic effect, which promotes the relaxation of smooth muscles in the ureters. This action is combined with a diuretic mechanism that increases urine volume and flow rate. The resulting physiological effect is the muscular relaxation that influences particle transit and a mechanical flushing action contributing to particle elimination.

Anti-Adherence and Epithelial Protection

The final domain involves mechanisms affecting the integrity of the urinary lining. The drug’s constituents exhibit anti-adherence properties, preventing both mineral crystals and uropathogenic bacteria from binding to the urothelial cells. This is supported by an anti-oxidant mechanism that contributes to the protection of renal tissue from cellular damage induced by reactive oxygen species (ROS).

Dosage and Administration Information

How Cystone is Used: Administration Guidelines

Cystone is an Ayurvedic proprietary medicine intended solely for oral administration, typically supplied as an uncoated tablet. Usage instructions are structured around specific dosing regimens and supportive measures.

Standard Dosing and Frequency

The standard adult regimen for conditions like urolithiasis (kidney stones) often begins with an initial phase of two tablets, three times daily (TID). This initial course typically lasts 3 to 4 months before transitioning to a lower maintenance dose of one tablet, twice daily (BID). For short-term symptom management, such as burning micturition, the TID frequency is often used until symptoms subside (e.g., within two weeks).

Age Group Condition Phase Dosing Frequency
Adult (Standard) Initial/Acute 2 tablets, three times daily (TID)
Adult (Maintenance) Post-Acute/Prevention 1 tablet, two or three times daily (BID/TID)

Administration Conditions and Adjustments

The medicine is generally taken after meals. Its administration is tied to a requirement for increased fluid intake, specifically consuming up to 2.0–2.5 liters of liquid per day.

Pediatric Dosing: Cystone is contraindicated for children under six years old. Specific dose adjustments are noted for older children: those aged 6–11 years use one tablet, TID, and those aged 12–15 years use one tablet, four times a day (QID).

Special Constraint: Cystone administration is not advisable in cases where a threatening urethral obstruction may occur due to very large stone size.

Recent Clinical Evidence

Recent Clinical Evidence

Clinical research on Cystone primarily focuses on its potential role in managing urolithiasis (kidney and urinary stones) and, to a lesser extent, urinary tract infections (UTIs).


Urolithiasis (Kidney/Urinary Stones)

Multiple randomized and comparative studies have investigated the use of this formulation, often as an adjuvant therapy in patients with urinary stones.

  • Stone Size and Clearance: Several trials have reported that the administration of Cystone was associated with a statistically significant reduction in mean stone size and may facilitate stone clearance, particularly for ureteric calculi. One meta-analysis of studies involving urolithiasis reported a significant decrease in stone size compared to placebo.
  • Stone Type Variation: The evidence is not uniform across all stone types. Some studies suggest it may be less effective in managing cystine or calcium oxalate stone recurrence, with certain trials reporting no significant change in stone burden or urinary chemistry in these specific patient groups over a one-year period.
  • Symptom Relief: Comparative studies, including one against the standard drug Tamsulosin, have suggested that the formulation may lead to an improvement in symptoms associated with urolithiasis, such as colicky pain, dysuria, and hematuria.

Urinary Tract Infections (UTIs)

Research has explored Cystone's use as an adjuvant therapy in UTIs. Some small, older trials reported that the addition of the formulation to a standard regimen (antibiotic plus alkalizer) was associated with a quicker symptomatic recovery compared to the standard regimen alone. This area, however, requires further high-quality, contemporary research to establish a clear benefit.

Safety and Tolerability

Across multiple clinical studies on urolithiasis and UTIs, Cystone was generally reported to be well tolerated. Reported adverse events were typically mild, non-serious, and occasional, including gastric irritation, dyspepsia, and flatulence. No severe adverse effects or mortality have been commonly reported in the examined clinical literature.

Frequently Asked Questions (FAQ)

Common questions about Cystone (FAQ)


Q: What specific type of kidney stones (e.g., calcium oxalate, uric acid) is Cystone associated with?

Official information indicates that the formulation’s actions include reducing the supersaturation of mineral salts, which is a key step in the formation of calcium oxalate stones. Studies have examined its use across various stone types, including research that notes variations in evidence regarding the recurrence of cystine stones.


Q: Is Cystone considered a drug or a dietary supplement in major regulatory regions?

According to official documentation, Cystone is regulated as an Ayurvedic proprietary medicine in its country of origin. This classification places it under traditional medical standards. In many international markets, the product is widely available for over-the-counter (OTC) use.


Q: Is there published clinical research or evidence on the effectiveness of Cystone?

Yes, official summaries of the product cite multiple randomized and comparative clinical studies that have investigated its properties. This research primarily focuses on Cystone’s potential role in managing urolithiasis (kidney stones) and, to a lesser extent, in supporting the management of urinary tract infections (UTIs).


Q: Does the mechanism of action of Cystone involve dissolving existing stones or mainly preventing new ones?

Official classification defines Cystone as both an antilithiatic agent and a lithotriptic agent. The antilithiatic property means it helps prevent the formation of new stones, while the lithotriptic action means it helps dissolve existing small stones and aids in their elimination.


Q: Is Cystone available over the counter, or does it require a prescription in most places?

The product is classified for use as an over-the-counter (OTC) medicine in many regions where it is distributed. This general availability means a prescription is not typically required.


Q: Is Cystone safe for long-term use, such as for preventing stone recurrence?

Official dosing documentation includes a lower maintenance dose intended for use following the initial treatment phase, suggesting its role in recurrence prevention. The total duration of use for prevention purposes is typically determined by a healthcare provider.


Q: What is the expected timeline for noticeable effects when taking Cystone for urinary discomfort?

Official dosing guidelines for short-term symptom management, such as burning micturition (painful urination), describe the use of the initial frequency until symptoms subside. This symptom-focused course often falls within a timeframe of up to two weeks.


Q: Is Cystone known to interact with common pain relievers or non-steroidal anti-inflammatory drugs (NSAIDs)?

The official regulatory interaction profile for the medicine states that no clinically significant drug interactions have been reported or formally documented with Cystone. This includes common substance classes such as pain relievers.


Q: Are there any specific dietary changes often recommended to support the intended effect of Cystone?

Official administration conditions stipulate that Cystone must be taken with a requirement for significantly increased fluid intake. Specifically, patients are advised to consume up to 2.0–2.5 liters of liquid per day during its administration.


Q: Does Cystone affect the body's mineral balance, such as calcium and phosphate levels in the urine?

Official pharmacological summaries and clinical evidence indicate that the formulation is involved in reducing the supersaturation of mineral salts. It can help regulate the urinary excretion of stone-forming substances, such as calcium, oxalate, and urate.

How should Cystone be stored and disposed of?

Storage Conditions

Cystone, as an Ayurvedic proprietary medicine, requires specific conditions to maintain the stability of its polyherbal components. The product must be stored in a cool place at a temperature not exceeding 30 C. To prevent degradation, it must be kept in a dry place and protected from direct sunlight and moisture.

Crucially, as with all medicines, the product must be stored out of the reach and sight of children.

Disposal Instructions

Official labeling does not provide product-specific flushing instructions. Therefore, disposal of unused or expired Cystone should follow general governmental guidelines for non-hazardous medicines.

The recommended method is to use authorized community drug take-back programs. If a take-back program is unavailable, the product may be mixed with an undesirable substance (such as used coffee grounds) and sealed in a bag for disposal in the household trash.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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