Candid-V6

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Candid-V6

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Medically reviewed

Laura Arias

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 Candid-V6

Property Description
Active ingredient Clotrimazole
Form Vaginal Tablet (Pessary)
Pharmacological class Azole Antifungal / Imidazole Derivative
General Purpose Counteracts fungal growth
Origin Synthetic Compound

What Type of Medicine is Candid-V6?

Candid-V6 is defined by its sole active ingredient, Clotrimazole, which functions as a broad-spectrum antifungal agent. The substance is a synthetic compound classified within the Azole antifungal pharmacological class, belonging specifically to the imidazole derivative family. This classification groups Clotrimazole with other agents that share a similar chemical foundation. Candid-V6 is manufactured by Glenmark Pharmaceuticals Ltd., a detail important for product identification, and is often available via prescription status depending on the specific country or jurisdiction. Azole derivatives, including Clotrimazole, act to disrupt the fungal growth cycle.

Composition and Localized Form

The medicine is supplied exclusively as a Vaginal Tablet, a specialized pharmaceutical preparation often referred to as a pessary. This specific dosage form is utilized for intravaginal administration, which facilitates a direct, localized treatment of the affected area. Candid-V6 is a single-ingredient product composed of the active agent Clotrimazole combined with the necessary solid pharmaceutical excipients required for the tablet’s controlled release and structural integrity. This localized strategy ensures high concentrations of the antifungal compound are delivered where the fungal presence is located, a methodology for facilitating therapeutic contact in topical infections.

General Purpose of this Antifungal Agent

The general purpose of this antifungal agent is to eliminate susceptible fungal organisms by compromising their structural vitality. The function of Clotrimazole is rooted in its ability to inhibit the biosynthesis of ergosterol, a critical component of the fungal cell membrane. By preventing the organism from building and maintaining its outer protective layer, the medicine stops the fungal cells from growing and multiplying. This imidazole class works by stopping the growth of fungi that cause infection. This action underscores the medicine's role in addressing the fungal infection through targeted cellular disruption.

Regulatory References

  1. Clotrimazole - StatPearls - NCBI Bookshelf
  2. Clotrimazole Vaginal: MedlinePlus Drug Information

What side effects are possible with Candid-V6?

Possible Side Effects and Safety Information

The safety profile for Candid-V6, a clotrimazole vaginal tablet, is primarily characterized by localized reactions at the application site, reflecting the product's minimal systemic absorption. The frequency of most adverse reactions is formally classified by regulatory authorities as Frequency Not Known, as these reports are typically based on post-marketing surveillance rather than controlled clinical studies.


Official Adverse Reaction Groupings

Adverse reactions are formally grouped by System-Organ Class (SOC) in regulatory documents:

  • Reproductive System and Breast Disorders: Includes vulvovaginal discomfort, pain, burning sensation, irritation, pruritus (itching), erythema (redness), and swelling.
  • Immune System Disorders: Documents allergic reactions (hypersensitivity), which include rare, potentially serious events such as Syncope (fainting), Hypotension (low blood pressure), and Dyspnea (shortness of breath).
  • Gastrointestinal Disorders: May include abdominal pain or nausea.

Localized adverse effects, such as a mild increase in vaginal burning or irritation, may be noted upon the initiation of treatment.


Safety-Related Restrictions

Official labeling defines key constraints and population-specific notes:

  • Contraindication: Candid-V6 is strictly contraindicated in individuals with a known hypersensitivity to clotrimazole or any of the product's excipients.
  • Latex Contraceptives: Laboratory testing suggests that excipients in the vaginal formulation may cause damage to latex contraceptives (condoms or diaphragms), potentially reducing their effectiveness. Alternative forms of contraception should be used.
  • Pregnancy and Lactation: Use during pregnancy or breastfeeding is advised only if clearly indicated by a healthcare professional, with specific note that the use of the applicator should be avoided during pregnancy.

The safety structure emphasizes local effects while mandating the disclosure of rare systemic risks and specific constraints related to latex products.

Overdose and Emergency Response

The official regulatory profile for Candid-V6 (Clotrimazole Vaginal Tablet) notes that acute intoxication is unlikely to occur following intended vaginal application due to the medicine's minimal systemic absorption. The primary scenario addressed in regulatory documents is the inadvertent oral ingestion of the tablet, which is the circumstance where clinical symptoms of overdose may become apparent. The potential documented manifestations in this context include dizziness, nausea, and vomiting.

When to Seek Immediate Medical Attention

Emergency medical assistance must be sought immediately following the accidental swallowing of the vaginal tablet. The official instructions state to contact a doctor or hospital emergency department immediately. Urgent medical evaluation is also explicitly required if severe signs of systemic hypersensitivity or allergic reactions develop, such as swelling of the face, throat, or tongue, difficulty breathing (dyspnoea), or sudden collapse (syncope).

Management and Supportive Care

Regulatory information confirms that no specific antidote is known for this product. Management focuses on supportive and symptomatic care. Procedural interventions, such as gastric lavage, are rarely required and should only be considered if severe clinical symptoms of overdose are present. If this intervention is undertaken, adequate airway protection must be ensured, as defined in the official regulatory documentation.

Therapeutic Uses of Candid-V6

What Candid-V6 Treats: Main Uses and Benefits

Candid-V6 is a localized treatment commonly used to manage the clinical manifestations and provides supportive relief from fungal infections of the vagina, primarily Vulvovaginal Candidosis (VVC), or vaginal thrush. The treatment is used in the management of candidal vaginitis. It is relevant in clinical settings marked by heightened patient distress associated with fungal overgrowth, addressing both acute and recurrent symptomatic episodes.


The primary therapeutic benefit is connected to its use across domains where additional symptomatic support is needed. This includes conditions presenting with acute episodes of intense vulvovaginal itching (pruritus), a painful burning sensation, and the presence of abnormal, thick, white discharge.

The medication is commonly used when symptoms intensify, providing assistance in managing these difficult manifestations. By addressing the fungal presence, it contributes to improved comfort and supports general well-being.


Quick Fact: Symptomatic Relief for VVC

The treatment is relevant in contexts involving a heightened symptom-related burden, helping to ease the overall symptoms linked to fungal tissue irritation, and is commonly used to help with both acute and recurrent episodes.

Eligibility and Restrictions for Use

Candid-V6 (Clotrimazole vaginal tablets) is primarily intended for adult women and girls 12 years of age and older to treat uncomplicated vulvovaginal candidiasis, commonly known as a yeast infection.

However, it is advised to consult a healthcare provider before use, or to avoid use entirely, if certain conditions or symptoms are present. For instance, do not use this product if you have a known allergy or hypersensitivity to clotrimazole or any other ingredients in the formulation.

Consult your doctor before starting treatment if you:

  • Have had more than three vaginal yeast infections within the last six months.
  • Have accompanying symptoms like fever, chills, abdominal pain, or foul-smelling vaginal discharge.
  • Are pregnant or breastfeeding.
  • Have a compromised immune system (e.g., due to HIV/AIDS or diabetes).
  • Are under 16 or over 60 years old.
Who Can Use Who Should Consult a Doctor / Avoid
Women 16–60 years old First-time infection diagnosis
Uncomplicated yeast infection Pregnant or breastfeeding patients
Patients with diabetes or HIV/AIDS
History of frequent infections (more than three in six months)
Allergy to clotrimazole or its components

What should I know about interactions with other medicines?

Interactions with other medicines and products

Although the systemic absorption of the active ingredient in Candid-V6 (clotrimazole) after vaginal use is generally low, interactions may occur with certain systemic medications and non-medicinal products.

Drug-Drug Interactions

Systemic Medicine Potential Interaction
Tacrolimus (oral) Increased plasma levels of Tacrolimus, which may lead to toxicity.
Sirolimus (oral) Increased plasma levels of Sirolimus, which may require dose adjustment.

Clotrimazole can inhibit the enzyme (CYP3A4) primarily responsible for metabolizing these oral immunosuppressant drugs. This inhibition can result in higher concentrations of Tacrolimus and Sirolimus in the bloodstream, particularly in patients such as those who have received an organ transplant. Due to the potential for serious adverse effects, individuals taking these immunosuppressants may require frequent monitoring of their blood levels.

Product-Product Interactions

  • Latex Contraceptives: The vaginal tablet or cream and its components may cause damage to barrier contraceptive devices made of latex, such as condoms and diaphragms. This physical interaction can reduce the effectiveness of these devices, increasing the risk of pregnancy or sexually transmitted disease transmission. Alternative contraceptive measures should be used for at least five days after the end of treatment.
  • Other Vaginal Products: Avoid the use of other intravaginal products, including tampons, douches, and spermicides, during the course of treatment. The simultaneous use of these items may interfere with the action of the medication.

Mechanism of Action

The action of Candid-V6 is strictly defined by its mechanism of targeting and disrupting the core biological processes essential for fungal cell vitality. This action is peripheral and local, concentrating its effect directly at the cellular interface.

Targeted Inhibition of Fungal Sterol Biosynthesis

The drug's primary mechanism involves the selective inhibition of lanosterol 14 alpha-demethylase, a critical Cytochrome P450 enzyme (CYP51) within the fungal cell. By blocking this enzyme, the drug prevents the synthesis of ergosterol, the primary sterol component of the fungal cell membrane.

Membrane Deconstruction and Inhibition of Fungal Replication

This targeted inhibition initiates a cascade where essential ergosterol is depleted and replaced by toxic, abnormal 14alpha-methylated sterols. These defective components compromise the membrane's structure, causing a profound loss of selective permeability that leads to the leakage of vital cellular contents. This biological damage inhibits the fungal organism's replication and growth processes, resulting in functional impairment or cellular lysis in a concentration-dependent manner.

Dosage and Administration Information

Administration Scope

Candid-V6 (Clotrimazole vaginal tablet) is administered strictly via the intravaginal route. Its use is defined by short-term courses. The dosing schedule typically involves a choice between a single-day, high-strength regimen or a multi-day course. The single-dose regimen uses one 500 mg vaginal tablet. Alternatively, multi-day regimens may involve either one 100 mg tablet daily for six consecutive days or two 100 mg tablets daily for three consecutive days.

Administration is scheduled once daily, preferably at bedtime, a timing intended to optimize tablet retention and dissolution, which relies on vaginal moisture. Procedurally, the tablet is typically inserted as high as possible into the vagina, a step facilitated by lying on the back with the legs slightly bent.

Official Use Constraints

Standard practice involves certain constraints during treatment: use involves avoiding the concurrent use of tampons, douches, spermicides, or other vaginal products, and sexual intercourse is generally avoided. The treatment course is typically completed before the onset of menstruation.

Specific age-group administration rules apply: for pregnant individuals, administration involves inserting the tablet using a finger instead of the applicator. If a dose is missed during a multi-day course, the tablet is inserted as soon as possible, with the next dose taken at the usual time.

Recent Clinical Evidence

Research Evidence / Overview of Studies for Candid-V6

Evidence for Use in Vulvovaginal Candidosis (VVC) and Candidal Vaginitis

The evidence landscape for Candid-V6 was studied for its evaluation in patients with fungal infections of the vagina, often referred to as Vulvovaginal Candidosis (VVC) or candidal vaginitis. Research primarily involves Randomized Controlled Trials (RCTs) and Comparative Clinical Trials. These study designs were used in trials assessing short-term or episodic symptom patterns.

The research examined two main outcomes: outcomes related to local symptoms (such as itching, burning, and discharge) and the monitoring of physiological strain or stress. Findings describe patterns observed in the studies where the reported changes in symptoms were monitored in relation to the measured change in the fungal presence. The body of research supporting this indication is consistently structured as high-level evidence.

Long-Term Studies and Follow-Up

The research exploring the use of this treatment is typically limited to short-term observation periods. Follow-up durations were focused on the one to two weeks immediately following the end of the treatment course. This time frame was used in research exploring how symptoms change over time.

Consequently, long-term effects are not fully established for this treatment. Follow-up durations were limited in many of the core studies, meaning that evidence is limited when assessing the durability of the findings or the potential relationship to future, recurrent episodes of VVC. The research structure does not provide full data concerning individual long-term outcomes.

Evidence in Specific Study Populations

The core clinical research for Candid-V6 was evaluated in specific groups of patients. The results apply only to the populations studied, which were predominantly adult and adolescent females presenting with a clinical diagnosis of VVC.

What Research Gaps and Uncertainty Remain

One key limitation is the limited data on recurrence prevention following the short-term course of treatment. Additionally, the research that examined this medicine mainly focused on the most common fungus (Candida albicans). Subgroup findings are uncertain when applied to less common, non-albicans Candida species, where findings were mixed in studies exploring these fungal types. Overall, while the evidence describes the pattern of outcomes in the studied groups over short time intervals, certainty remains low for long-term effects and outcomes in specific, less-studied populations. The existing studies provide context but not individual predictions.

Key Studies & References

  1. Clotrimazole Vaginal Tablet: FDA Approved Drug Labeling and Product Information

Frequently Asked Questions (FAQ)

Common questions about Candid-V6 (FAQ)


Q: Is Candid-V6 the same kind of medicine as other treatments I have seen?

Candid-V6 is defined by its active ingredient, which is classified as an Azole antifungal agent. This pharmacological group includes various agents that share a similar chemical foundation used to treat fungal infections. Official documentation categorizes the active component based on this specific chemical class.


Q: What are the most common things people feel when they take Candid-V6?

According to the official product information, common side effects that have been reported are primarily localized reactions at the application site. These may include vulvovaginal discomfort, a burning sensation, irritation, itching, or pain. Less commonly, effects such as abdominal pain or nausea may be reported.


Q: What should I do if my symptoms seem to get worse after starting Candid-V6?

Official guidance indicates that contact should be made with a healthcare professional if signs of increased local irritation, such as redness, itching, or blistering, occur during treatment. It is also noted that contact should be made if symptoms fail to improve after the expected treatment period has passed.


Q: What are the signs that Candid-V6 might not be working for someone?

Failure to achieve noticeable symptom improvement after a specified timeframe, such as four weeks following the start of treatment, is noted in regulatory documents as a reason to notify a healthcare professional. This is a general marker for potentially seeking further evaluation.


Q: Does using Candid-V6 require changes to diet or lifestyle?

Official labeling states that certain vaginal products, including tampons, douches, and spermicides, should be avoided during the treatment course. Official documentation also advises that sexual intercourse should be avoided. Regulatory information does not specify required changes to general diet during the treatment period.


Q: How long does it usually take before Candid-V6 starts to work?

Studies on the drug’s performance show that the single-dose tablet acts as a local depot. This allows fungicidal (fungus-eliminating) concentrations of the active ingredient to persist in the vagina for up to three days following a single application.


Q: What is the expected length of time Candid-V6 stays in my system?

Systemic absorption (entering the bloodstream) of the active ingredient is low, typically 3% to 10% of the dose. The absorbed amount is rapidly metabolized by the liver and then excreted, with peak levels in the bloodstream being reached one to two days after application.


Q: Is Candid-V6 available without a prescription in some countries?

The active ingredient in the vaginal tablet dosage form is commonly available as an Over-The-Counter (OTC) product in certain jurisdictions. However, its classification may vary depending on the country and the strength of the product.


Q: Does Candid-V6 contain any penicillin or antibiotics?

No. The active ingredient in Candid-V6 is defined and classified as an antifungal medication and an imidazole derivative. It is not classified as a penicillin or an antibacterial antibiotic agent.


Q: Can Candid-V6 be taken if a person is already taking blood pressure medication?

Due to the potential for interaction, the product may increase the blood levels of specific oral systemic medications, such as the blood pressure medicine amlodipine. Official information indicates that monitoring by a healthcare professional may be necessary when these medications are used concurrently.


Q: Can men use Candid-V6 for certain conditions?

Candid-V6 vaginal tablets are specifically indicated for treating vulvovaginal candidiasis, a condition that affects females. The core clinical research populations evaluated for this product were predominantly adult and adolescent females presenting with this diagnosis.


Q: Does Candid-V6 have any known effects on fertility?

Official information indicates that using the active ingredient is generally not expected to make it harder for a woman to become pregnant. However, information specifically regarding potential effects on male fertility is limited in available documentation.


Q: Is it possible to be resistant to the effects of Candid-V6?

Regulatory information suggests that resistance to the active ingredient is considered rare. Some specific strains of less common Candida organisms have been reported to show primary resistance in studies.


Q: Does using Candid-V6 make someone more likely to get the condition again later?

Clinical research exploring the long-term prevention of recurrence following a course of treatment is limited. One study on monthly prophylactic use did show a modest protective effect, reducing the rate of recurrence in the study population.


Q: How long after finishing the course of Candid-V6 can a person resume normal activity?

Official instruction states that alternative contraceptive measures are advised to be considered for at least five days after the end of treatment. This is because components of the product may damage latex contraceptives (condoms or diaphragms), potentially reducing their effectiveness.


Q: Are there different strengths or versions of Candid-V6 available?

Yes, the vaginal tablet is available in multiple strengths, including 100 mg, 200 mg, and 500 mg. These different strengths are used for various single-day or multi-day treatment regimens defined in official guidelines.


Q: Does Candid-V6 contain any artificial colors or common allergens?

Ingredient lists detail the various excipients (inactive ingredients) in the formulation, such as lactose. Hypersensitivity (allergic) reactions to the active ingredient or any excipient are listed in the official warnings as a contraindication.


Q: Is the medication considered safe for people with lactose intolerance?

Regulatory ingredient lists for some formulations of the vaginal tablet confirm that lactose is included as an auxiliary, or inactive, ingredient. Official labeling makes the full ingredient list available for review by individuals with specific intolerances.


Q: What is the risk of developing a serious side effect with Candid-V6?

Serious adverse effects, such as syncope (fainting) or hypotension (low blood pressure), are generally categorized as systemic allergic reactions. These events are reported in rare cases, often with a frequency classified as 'not known' based on post-marketing surveillance.


Q: Has Candid-V6 been approved in European countries as well as the US?

The active ingredient has received regulatory approval in the United States (FDA) and is referenced in official drug safety documents from multiple European agencies. This indicates that the product has approval and recognized status across several international jurisdictions.

How should Candid-V6 be stored and disposed of?

How to Store and Dispose of Candid-V6 (Clotrimazole Vaginal Tablets)

Candid-V6 must be stored and disposed of according to regulatory guidelines to ensure product stability and safety. The following instructions are based on official product labeling.


Official Storage Requirements

Condition Requirement
Temperature Store at room temperature, typically defined as not exceeding 30 C. The product must not be frozen.
Protection Keep the tablets in the original, tightly closed package to protect them from light and moisture.
Child Safety The medication must be kept out of the sight and reach of children.

Disposal Instructions

Any unused or expired Candid-V6 and the used applicator must be handled in accordance with local regulatory requirements.

  • Do not flush the used applicator or unused medicine down the toilet.
  • If local take-back programs are unavailable, disposal should follow official guidance, such as mixing the product with an undesirable substance (e.g., used coffee grounds) before sealing it and discarding it in the household trash.

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

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