Sepia-Plus (Drops) Instructions for Use
Marketing Authorization Holder
Doctor N, LLC (Russia)
Dosage Form
| Sepia-Plus | Homeopathic oral drops: 25 ml or 50 ml dropper bottle |
Dosage Form, Packaging, and Composition
Homeopathic oral drops are transparent, colorless, with a faint alcoholic odor.
| Sepia officinalis (Sepia) C6 |
| Aurum metallicum C12 |
| Strychnos ignatii (Ignatia) C6 |
| Phosphorus C12 |
| Lycopodium clavatum (Lycopodium) C6 |
| Lytta vesicatoria (Cantharis) C6 |
| Cimicifuga racemosa (Cimicifuga) C6 |
| Natrium chloratum C12 |
Excipients: ethanol about 30 % (vol.).
25 ml – orange glass bottles (1) with dropper caps – cardboard boxes.
50 ml – orange glass bottles (1) with dropper caps – cardboard boxes.
Clinical-Pharmacological Group
Homeopathic preparation used for menstrual cycle disorders, mastopathy and premenstrual syndrome
Pharmacotherapeutic Group
Homeopathic agent
Pharmacological Action
A multicomponent homeopathic preparation, the action of which is due to the components that make up its composition.
Indications
- Dysmenorrhea in combination with premenstrual syndrome.
ICD codes
| ICD-10 code | Indication |
| N94.3 | Premenstrual tension syndrome |
| N94.4 | Primary dysmenorrhea |
| N94.5 | Secondary dysmenorrhea |
| ICD-11 code | Indication |
| GA34.3 | Dysmenorrhea |
| GA34.40 | Premenstrual tension syndrome |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Take the preparation three times daily for a duration of 12 weeks.
Administer each dose 30 minutes before or one hour after a meal, or in between meals.
For a single dose, always dilute 8 drops in 100 ml of water before ingestion.
Adverse Reactions
Allergic reactions are possible.
Discontinue use immediately and consult a physician if any signs of hypersensitivity, such as skin rash, itching, or swelling, occur.
Contraindications
- Hypersensitivity to any component of the preparation.
- Age under 18 years.
Use with caution in patients with liver diseases, alcoholism, traumatic brain injury, and brain diseases.
Use in Pregnancy and Lactation
Not recommended due to the content of ethanol (ethyl alcohol) in the preparation.
Use in Hepatic Impairment
Use with caution in liver diseases.
Pediatric Use
Contraindicated in children under 18 years of age.
Special Precautions
If there is no therapeutic effect, as well as if side effects not described in the preparation instructions appear, you should consult a doctor.
During the use of the preparation, do not abuse alcoholic beverages or coffee.
It is not recommended to take preparations containing mint.
The maximum daily dose of the preparation contains 0.28 g of absolute alcohol.
Effect on the ability to drive vehicles and machinery
No effect.
Overdose
No cases of overdose have been reported to date.
In the event of accidental ingestion of a significantly larger than prescribed dose, seek immediate medical attention.
Symptoms of overdose may be related to ethanol content and include dizziness, nausea, and coordination disturbances.
Drug Interactions
Simultaneous use with other medicinal products is possible.
No specific, clinically significant drug interactions are known.
Inform your physician about all other medications you are taking, including over-the-counter products and herbal supplements.
Storage Conditions
Store in a place protected from light, at a temperature not exceeding 25°C (77°F). Keep out of reach of children.
Shelf Life
Shelf life – 5 years.
Dispensing Status
Over-the-counter.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer