Doktor MOM® herbal cough lozenges (Pastilles) Instructions for Use
Marketing Authorization Holder
J&JTL, LLC (Russia)
Manufactured By
Unique Pharmaceutical Laboratories (A Division of J. B. Chemicals & Pharmaceuticals Ltd.) (India)
Contact Information
J&JTL LLC (Russia)
ATC Code
R05CA10 (Expectorants in combination)
Dosage Forms
| Doktor MOM® herbal cough lozenges | Pastilles (berry): 20 pcs. | |
| Pastilles (orange): 20 pcs. | ||
| Pastilles (strawberry): 20 pcs. | ||
| Pastilles (lemon): 20 pcs. | ||
| Pastilles (raspberry): 20 pcs. |
Dosage Form, Packaging, and Composition
Pastilles (orange) are orange in color, round, biconvex; the presence of air bubbles in the pastilles and uneven edges is allowed.
| 1 pastille | |
| Dry extracts (extractant – water), isolated from plant materials | |
| Licorice (Glycyrrhiza glabra) roots | 15 mg, |
| Equivalent to dry extract (5:1) | 3 mg |
| Ginger (Zingiber officinale) rhizomes | 10 mg, |
| Equivalent to dry extract (10:1) | 1 mg |
| Emblica (Emblica officinalis) fruits | 10 mg, |
| Equivalent to dry extract (4:1) | 2.5 mg |
| Levomenthol | 7 mg |
Excipients: sucrose – 1623.5 mg, liquid dextrose – 1037 mg, glycerol – 1.5 mg, citric acid monohydrate – 20 mg, orange-mint flavor – 4.07 mg, mint flavor – 0.012 mg, sunset yellow FCF dye – 0.125 mg.
4 pcs. – aluminum strips (5) – cardboard packs.
Pastilles (lemon) are from greenish-yellow to yellow in color, round, biconvex; the presence of air bubbles in the pastilles and uneven edges is allowed.
| 1 pastille | |
| Dry extracts (extractant – water), isolated from plant materials | |
| Licorice (Glycyrrhiza glabra) roots | 15 mg, |
| Equivalent to dry extract (5:1) | 3 mg |
| Ginger (Zingiber officinale) rhizomes | 10 mg, |
| Equivalent to dry extract (10:1) | 1 mg |
| Emblica (Emblica officinalis) fruits | 10 mg, |
| Equivalent to dry extract (4:1) | 2.5 mg |
| Levomenthol | 7 mg |
Excipients: sucrose – 1623.5 mg, liquid dextrose – 1037 mg, glycerol – 1.5 mg, citric acid monohydrate – 25 mg, lemon oil – 3.75 mg, mint flavor – 0.125 mg, quinoline yellow dye – 0.1 mg.
4 pcs. – aluminum strips (5) – cardboard packs.
Pastilles (strawberry) are from red to cherry-red in color, round, biconvex; the presence of air bubbles in the pastilles and uneven edges is allowed.
| 1 pastille | |
| Dry extracts (extractant – water), isolated from plant materials | |
| Licorice (Glycyrrhiza glabra) roots | 15 mg, |
| Equivalent to dry extract (5:1) | 3 mg |
| Ginger (Zingiber officinale) rhizomes | 10 mg, |
| Equivalent to dry extract (10:1) | 1 mg |
| Emblica (Emblica officinalis) fruits | 10 mg, |
| Equivalent to dry extract (4:1) | 2.5 mg |
| Levomenthol | 7 mg |
Excipients: sucrose – 1623.5 mg, liquid dextrose – 1037 mg, glycerol – 1.5 mg, citric acid monohydrate – 18 mg, strawberry flavor – 7.5 mg, ponceau 4R dye – 1.25 mg.
4 pcs. – aluminum strips (5) – cardboard packs.
Pastilles (raspberry) are from red to dark red in color, round, biconvex; the presence of air bubbles in the pastilles and uneven edges is allowed.
| 1 pastille | |
| Dry extracts (extractant – water), isolated from plant materials | |
| Licorice (Glycyrrhiza glabra) roots | 15 mg, |
| Equivalent to dry extract (5:1) | 3 mg |
| Ginger (Zingiber officinale) rhizomes | 10 mg, |
| Equivalent to dry extract (10:1) | 1 mg |
| Emblica (Emblica officinalis) fruits | 10 mg, |
| Equivalent to dry extract (4:1) | 2.5 mg |
| Levomenthol | 7 mg |
Excipients: sucrose – 1623.5 mg, liquid dextrose – 1037 mg, glycerol – 1.5 mg, raspberry flavor – 6.25 mg, azorubine dye – 0.1 mg.
4 pcs. – aluminum strips (5) – cardboard packs.
Pastilles (berry) are from pinkish-brown to brown in color, round, biconvex; the presence of air bubbles in the pastilles and uneven edges is allowed.
| 1 pastille | |
| Dry extracts (extractant – water), isolated from plant materials | |
| Licorice (Glycyrrhiza glabra) roots | 15 mg, |
| Equivalent to dry extract (5:1) | 3 mg |
| Ginger (Zingiber officinale) rhizomes | 10 mg, |
| Equivalent to dry extract (10:1) | 1 mg |
| Emblica (Emblica officinalis) fruits | 10 mg, |
| Equivalent to dry extract (4:1) | 2.5 mg |
| Levomenthol | 7 mg |
Excipients: sucrose – 1623.5 mg, liquid dextrose – 1037 mg, glycerol – 1.5 mg, citric acid monohydrate – 3 mg, berry flavor – 7 mg, azorubine dye – 0.025 mg, brilliant blue FCF dye – 0.005 mg.
4 pcs. – aluminum strips (5) – cardboard packs.
Clinical-Pharmacological Group
Herbal expectorant
Pharmacotherapeutic Group
Herbal expectorant
Pharmacological Action
A combined herbal preparation with expectorant and anti-inflammatory action. The action of the preparation is due to the properties of its constituent components.
Licorice root extract has expectorant, anti-inflammatory, and antispasmodic action.
Ginger rhizome extract has anti-inflammatory and analgesic effects.
Emblica fruit extract has anti-inflammatory and antipyretic action.
Menthol, which is part of the preparation, has antispasmodic and antiseptic action.
Indications
Symptomatic therapy of acute and chronic diseases of the upper respiratory tract accompanied by dry cough
- Pharyngitis;
- Laryngitis (including professional “lecturer’s” laryngitis);
- Tracheitis;
- Bronchitis.
ICD codes
| ICD-10 code | Indication |
| J02 | Acute pharyngitis |
| J04 | Acute laryngitis and tracheitis |
| J20 | Acute bronchitis |
| J31.2 | Chronic pharyngitis |
| J37 | Chronic laryngitis and laryngotracheitis |
| J42 | Unspecified chronic bronchitis |
| R05 | Cough |
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. |
Dissolve the pastilles slowly in the mouth. Do not chew or swallow whole.
For adults only. Administer one pastille every two hours as needed for symptom relief.
The maximum daily dose is 10 pastilles. Strictly adhere to this limit to avoid excessive intake.
The recommended treatment course is two to three weeks.
Discontinue use and consult a physician if symptoms persist, worsen, or if new symptoms appear after two weeks.
Monitor patients with diabetes mellitus due to the sucrose and dextrose content; each pastille contains approximately 2.66 g of carbohydrates (0.22 XE).
This product is contraindicated in individuals under 18 years of age.
Adverse Reactions
Possible allergic reactions.
Contraindications
- Hypersensitivity to the components of the preparation;
- Sucrase/isomaltase deficiency, fructose intolerance, glucose-galactose malabsorption;
- Children under 18 years of age (due to lack of clinical data).
With caution
Patients with diabetes mellitus.
Use in Pregnancy and Lactation
The preparation is not recommended for use during pregnancy and breastfeeding due to the lack of clinical data.
Pediatric Use
Contraindicated for use in children under 18 years of age.
Special Precautions
The preparation contains sugar, which should be taken into account by patients with diabetes mellitus, as well as persons on a low-calorie diet. One pastille contains 2.66 g of carbohydrates, which corresponds to 0.22 XE (bread units).
If the symptoms of the disease worsen, persist, or new symptoms appear, it is necessary to stop taking the preparation and consult a doctor.
Do not chew or swallow the pastille whole.
Keep out of reach of children. If a child swallows the preparation, seek medical help immediately.
If the medicinal product has deteriorated or the expiration date has passed, it should not be disposed of in sewage or on the street. The preparation should be placed in a bag and disposed of in a trash container. These measures will help protect the environment.
Effect on the ability to drive vehicles and machinery
There are no data on the effect of the preparation on the ability to perform potentially hazardous activities that require increased concentration and speed of psychomotor reactions (driving vehicles, working with moving machinery, work of a dispatcher, operator).
Overdose
No cases of overdose with the preparation have been reported to date.
Drug Interactions
Concomitant use with antitussive drugs, as well as with drugs that reduce sputum formation, is not recommended, as this makes it difficult to expel liquefied sputum.
Storage Conditions
The preparation should be stored out of the reach of children at a temperature not exceeding 30°C (86°F).
Shelf Life
The shelf life is 3 years. Do not use after the expiration date.
Dispensing Status
The preparation is available without a prescription.
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
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