Corvalol (Tablets, Drops) Instructions for Use
ATC Code
N05CM (Other hypnotic and sedative drugs)
Clinical-Pharmacological Group
Drug with sedative and antispasmodic action
Pharmacotherapeutic Group
Psycholeptics; hypnotics and sedatives; other hypnotics and sedatives
Pharmacological Action
A combined drug, the action of which is determined by the properties of its constituent substances.
It has a sedative and antispasmodic action. It facilitates the onset of natural sleep.
Ethyl ester of α-bromoisovaleric acid has a sedative (similar to the effect of valerian) and antispasmodic action.
Phenobarbital enhances the sedative effect of other components, helps reduce excitation of the central nervous system and facilitates the onset of sleep.
In addition to the main components listed above (highlighted in italics), some preparations contain peppermint oil in their composition, which has a reflex vasodilating and antispasmodic action.
In addition to the main components listed above (highlighted in italics), some preparations contain levomenthol solution in menthyl isovalerate (Validol) – a reflex-acting coronary dilator that causes a sedative effect. The reflex vasodilating action is due to the irritation of sensitive nerve endings. It stimulates the production and release of enkephalins, endorphins and a number of other peptides, histamine, kinins (due to irritation of the receptors of the mucous membrane), which are actively involved in the regulation of vascular permeability and the formation of pain sensations.
Indications
As a sedative and vasodilator for the following diseases: functional disorders of the cardiovascular system (cardialgia, sinus tachycardia, increased blood pressure); insomnia (difficulty falling asleep); neurotic conditions; autonomic lability; irritability; hypochondriacal syndrome.
As an antispasmodic agent: spasm of the gastrointestinal tract musculature (intestinal and biliary colic).
ICD codes
| ICD-10 code | Indication |
| F45.2 | Hypochondriacal disorder |
| F45.3 | Somatoform dysfunction of the autonomic nervous system |
| F48.0 | Neurasthenia |
| F48.9 | Unspecified neurotic disorder |
| F51.0 | Nonorganic insomnia |
| K80 | Cholelithiasis [cholelithiasis] (including biliary colic) |
| R00.0 | Tachycardia, unspecified (including nodal (sinus) NOS) |
| R03.0 | Elevated blood-pressure reading without diagnosis of hypertension |
| R07.2 | Pain in the heart region |
| R10.4 | Other and unspecified abdominal pain (colic) |
| R45.4 | Irritability and anger |
| ICD-11 code | Indication |
| 6A8Z | Affective disorders, unspecified |
| 6B21.0 | Dysmorphic disorder with satisfactory or preserved insight |
| 6B21.1 | Dysmorphic disorder with reduced or absent insight |
| 6B21.Z | Body dysmorphic disorder, unspecified |
| 6B23.Z | Hypochondriasis, unspecified |
| 6B6Z | Dissociative disorders, unspecified |
| 6C20.Z | Bodily distress disorder, unspecified |
| 7A00 | Chronic insomnia |
| 7A01 | Acute insomnia |
| 7A0Z | Insomnia disorders, unspecified |
| DC11.Z | Cholelithiasis, unspecified |
| DD93.1 | Infantile colic |
| MB24.C | Irritability |
| MC80.0Z | Elevated blood pressure without diagnosis of hypertension, unspecified |
| MC81.Z | Abnormalities of heart rhythm, unspecified |
| MC86 | Precordial pain |
| MD81.4 | Other and unspecified abdominal pain |
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. |
Tablets, Drops
Orally, before meals, 15-30 drops, previously dissolved in a small amount (30-50 ml) of water, 2-3 times/day. The single dose, if necessary (for example, with tachycardia), can be increased to 40-50 drops.
For children – 3-15 drops/day (depending on age and the clinical picture of the disease).
The duration of the drug use is determined by the doctor individually.
Adverse Reactions
Drowsiness, dizziness, decreased ability to concentrate, allergic reactions.
With long-term use – chronic bromine poisoning (depression, apathy, rhinitis, conjunctivitis, hemorrhagic diathesis, impaired coordination of movements); drug dependence.
Contraindications
Hypersensitivity; severe hepatic and/or renal failure; lactation period (breastfeeding).
Use in Pregnancy and Lactation
If it is necessary to prescribe Corvalol during lactation, the issue of discontinuing breastfeeding should be decided.
Use with caution during pregnancy.
Use in Hepatic Impairment
Contraindicated in severe hepatic failure.
Use in Renal Impairment
Contraindicated in severe renal failure.
Pediatric Use
Use is possible according to the dosing regimen.
Special Precautions
During the treatment period, caution should be exercised when driving vehicles and engaging in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
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 DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Tablets: 10, 30, or 50 pcs.
Marketing Authorization Holder
Farmak, JSC (Ukraine)
Dosage Form
| Corvalol Forte | Tablets: 10, 30, or 50 pcs. |
Dosage Form, Packaging, and Composition
Tablets white, round, biconvex.
| 1 tab. | |
| Ethyl bromisovalerinate | 12.42 mg |
| Phenobarbital | 11.34 mg |
| Peppermint oil | 0.88 mg |
Excipients: lactose monohydrate – 285.25 mg, magnesium stearate – 4 mg, betadex (beta-cyclodextrin) – 85.71 mg, acesulfame K – 0.4 mg.
10 pcs. – blisters (1) – cardboard packs.
10 pcs. – blisters (3) – cardboard packs.
10 pcs. – blisters (5) – cardboard packs.
Oral drops: bottle 25 ml
Marketing Authorization Holder
Obnovlenie Pfc, JSC (Russia)
Dosage Form
| Corvalol Renewal | Oral drops: bottle 25 ml |
Dosage Form, Packaging, and Composition
Oral drops in the form of a transparent, colorless liquid with a characteristic odor.
| 100 ml | |
| Ethylbromisovalerinate (ethyl ester of alpha-bromoisovaleric acid) | 2000 mg |
| Phenobarbital | 1826 mg |
| Peppermint leaf essential oil | 142 mg |
Excipients: ethanol (ethyl alcohol) 95% – 79 ml, sodium hydroxide solution 1M – to pH 8.0-8.5, purified water – up to 100 ml.
25 ml – dark glass bottles (1) with a dropper cap – cardboard packs.
Ingavirin capsules 90mg, 10pcs
Nootropil pills 800mg, 30pcs
Cavinton Comfort, dispersible pills 10mg 90pcs
Picamilon pills 50mg, 60pcs
Actovegin pills 200mg, 50pcs
OKI, sachets 80mg 2g, 12pcs
Mildronate capsules 500mg, 90pcs
Belosalic, lotion solution for external use spray 100ml 