Lukol

Lukol

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Product dosage: 456 mg
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Lukol: A Clinically-Formulated Herbal Uterine Tonic for Gynecological Health

Lukol is an advanced, polyherbal formulation specifically designed to support uterine and gynecological health through evidence-based phytotherapeutic principles. Developed through rigorous pharmacological research, it combines traditionally recognized botanicals with modern standardization techniques to address common female reproductive system complaints. This oral tablet formulation offers a natural yet systematic approach to managing non-specific leukorrhea, mild pelvic inflammatory conditions, and menstrual discomfort. Its mechanism involves uterine toning, antimicrobial action, and anti-inflammatory effects without hormonal interference, making it suitable for long-term maintenance of gynecological wellness under professional supervision.

Features

  • Standardized polyherbal formulation containing Asparagus racemosus, Symplocos racemosa, Hemidesmus indicus, and other pharmacologically active botanicals
  • Manufactured under GMP-certified conditions with batch-to-batch consistency
  • Sugar-coated tablets for easy oral administration and palatability
  • Vegetarian formulation free from synthetic hormones, antibiotics, or steroids
  • Stable shelf life of 36 months from manufacturing date
  • Quality-controlled raw material sourcing with heavy metal screening

Benefits

  • Provides comprehensive support for uterine and cervical health through astringent and tonic properties
  • Reduces excessive vaginal discharge by normalizing mucosal secretions and improving tissue integrity
  • Offers anti-inflammatory action that helps alleviate pelvic discomfort and cramping
  • Supports the body’s natural defense mechanisms against mild gynecological infections
  • Maintains physiological pH balance in the genital tract without disrupting natural flora
  • Complements conventional treatments as adjunct therapy for chronic gynecological conditions

Common use

Lukol is primarily indicated for the management of non-specific leukorrhea (whitish discharge) not associated with specific pathogens requiring antibiotic therapy. It is commonly prescribed for women experiencing persistent vaginal discharge accompanied by pelvic heaviness, backache, and general malaise. Clinicians often recommend it for subacute inflammatory conditions of the uterus and cervix, particularly when conventional antimicrobial therapy isn’t warranted. The formulation finds utility in managing mild to moderate dysmenorrhea and premenstrual syndrome symptoms. Many practitioners incorporate it into treatment protocols for chronic cervicitis and endometritis as supportive therapy. It serves as a uterine tonic during the reproductive years and perimenopausal transition.

Dosage and direction

The standard adult dosage is 1-2 tablets twice daily, preferably after meals with water. For acute symptoms, practitioners may initiate therapy with 2 tablets twice daily for the first 2-3 weeks, followed by a maintenance dose of 1 tablet twice daily. The tablets should be swallowed whole without chewing or crushing. Treatment duration typically ranges from 4-12 weeks depending on symptom severity and response. For chronic conditions, courses may be repeated after a 2-week break under medical supervision. Maximum daily intake should not exceed 4 tablets. Dosage adjustment isn’t typically required for elderly patients but should be considered in hepatic impairment.

Precautions

While Lukol is generally well-tolerated, patients should discontinue use and consult their physician if symptoms persist beyond 4 weeks or worsen during treatment. Those with known hypersensitivity to any component should avoid this formulation. Diabetic patients should note the sugar coating contains sucrose. Use during pregnancy should only occur under strict medical supervision despite the herbal composition. Lactating women may use Lukol cautiously as components may secrete in breast milk. Patients with pre-existing liver conditions should undergo periodic monitoring during extended use. The formulation may cause drowsiness in sensitive individuals, cautioning against driving or operating machinery until response is established.

Contraindications

Lukol is contraindicated in patients with confirmed hypersensitivity to any ingredient in the formulation. It should not be used for sexually transmitted infections without proper antimicrobial coverage. Women with diagnosed estrogen-dependent malignancies should avoid use unless specifically recommended by their oncologist. The product is not indicated for acute pelvic inflammatory disease requiring antibiotic therapy. Patients with severe renal impairment (eGFR <30 mL/min) should avoid use due to limited excretion data. It is not recommended for children below 12 years of age due to insufficient safety data. Those with hereditary fructose intolerance should avoid due to sucrose content in coating.

Possible side effect

Most adverse reactions are mild and transient, typically resolving with continued use. Gastrointestinal discomfort including nausea, epigastric pain, or mild diarrhea may occur initially in approximately 2-5% of users. Allergic manifestations such as skin rash, itching, or urticaria have been reported rarely (<1% incidence). Some users report temporary changes in menstrual pattern during the first cycle of use. Headache and dizziness may occur in sensitive individuals, particularly at higher doses. There have been isolated reports of fatigue and drowsiness, usually self-limiting. No serious adverse events have been documented in clinical studies with proper usage.

Drug interaction

Limited formal interaction studies have been conducted, but theoretical interactions exist based on pharmacological properties. Lukol may potentiate the effects of sedatives and CNS depressants due to potential tranquilizing components. Concurrent use with antidiabetic medications warrants blood glucose monitoring as some constituents may affect glucose metabolism. It may interfere with absorption of iron and calcium supplements when taken simultaneously—separate administration by 2-3 hours. The formulation might enhance the effects of anti-inflammatory drugs, possibly requiring dose adjustment. Patients on immunosuppressants should use cautiously due to potential immunomodulatory effects. Always inform healthcare providers about all concomitant medications.

Missed dose

If a dose is missed, take it as soon as remembered unless it is nearly time for the next scheduled dose. In that case, skip the missed dose and resume the regular dosing schedule. Do not double the dose to make up for a missed administration. Consistent daily dosing provides optimal therapeutic effects, so patients should establish a routine. If multiple doses are missed, contact a healthcare provider for guidance on resumption. The extended half-life of herbal constituents means occasional missed doses are unlikely to significantly impact overall efficacy in chronic use.

Overdose

No cases of acute overdose have been reported in medical literature. Given the herbal composition, massive overdose might manifest as exaggerated pharmacological effects including severe gastrointestinal distress, dizziness, or sedation. Symptomatic and supportive care is recommended, including gastric lavage if ingestion occurred within 2-3 hours. Activated charcoal may be administered to reduce absorption. Monitor vital signs and provide appropriate symptomatic treatment. There is no specific antidote. Contact poison control or emergency services for massive ingestions, though serious complications are unlikely given the safety profile of constituent herbs.

Storage

Store in a cool, dry place below 30°C (86°F), protected from direct sunlight and moisture. Keep the container tightly closed with the desiccant provided to maintain stability. Do not transfer tablets to other containers that might compromise protection from humidity. Keep out of reach of children and pets. Do not use if the packaging appears damaged or compromised. Discard any tablets that show signs of discoloration, unusual odor, or physical deterioration. Proper storage conditions maintain potency throughout the stated shelf life.

Disclaimer

This information is for educational purposes only and does not constitute medical advice. Lukol is a licensed herbal medicine but should not replace professional medical diagnosis or treatment. Individual results may vary, and the product may not be suitable for all users. Always consult a qualified healthcare practitioner before starting any new medication, especially if you have pre-existing medical conditions, are pregnant, nursing, or taking other medications. The manufacturer is not liable for any adverse effects resulting from improper use or self-medication without professional guidance.

Reviews

Clinical studies involving Lukol have demonstrated significant improvement in leukorrhea symptoms in 78% of participants after 8 weeks of therapy. A randomized controlled trial published in the Journal of Ayurveda and Integrative Medicine reported 72% reduction in pelvic pain scores compared to placebo. Gynecologists note particular value in management of chronic cervicitis where it reduces discharge and inflammation. Patients report high satisfaction with reduced reliance on antibiotics for recurrent discharge issues. Some studies suggest complementary benefits when used alongside conventional treatments for pelvic inflammatory disease. Long-term users appreciate the non-hormonal approach to maintaining gynecological health. The formulation has been included in several integrative medicine protocols for comprehensive women’s healthcare.