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Snorstop (Tablets) Instructions for Use

Marketing Authorization Holder

Green Pharmaceuticals, Inc. (USA)

Manufactured By

Botanical Laboratories (USA)

Dosage Form

Bottle OTC Icon Snorstop Homeopathic sublingual tablets: 20 pcs.

Dosage Form, Packaging, and Composition

Homeopathic sublingual tablets round, biconvex, white in color, with an engraving “H” or “SS”.

Atropa belladonna (Belladonna) D6
Ephedra vulgaris D6
Hydrastis canadensis D6
Potassium dichromate D6
Teucrium marum D6
Histaminum hydrochloricum D12
Nux vomica D4, D6

Excipients: lactose, magnesium stearate.

20 pcs. – Al/PVC blisters (1) – cardboard packs.

Clinical-Pharmacological Group

Homeopathic preparation used for snoring syndrome

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

Homeopathic preparation.

Indications

  • Use as a symptomatic remedy for the reduction of snoring intensity during sleep.

The preparation is intended for the temporary management of simple, non-apneic snoring. It is not a treatment for the underlying cause.

ICD codes

ICD-10 code Indication
R06.5 Mouth breathing (snoring)
ICD-11 code Indication
MD11.8Z Mouth breathing, unspecified

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.

Administer once daily immediately before bedtime. Place the tablet sublingually and allow it to dissolve completely; do not chew or swallow whole.

For adults with a body weight up to 72 kg, the dose is 1 tablet. For adults with a body weight over 72 kg, the dose is 2 tablets.

If snoring severity decreases, reduce the frequency of administration to every other day. Do not exceed the recommended single dose.

Adverse Reactions

Allergic reactions, including skin rash, itching, urticaria, and angioedema, are possible. Discontinue use immediately and seek medical attention if any signs of hypersensitivity occur.

Due to the homeopathic nature of the product and high dilutions, other adverse reactions are not expected. Report any suspected adverse reactions to a healthcare professional.

Drug Interactions

Formal drug interaction studies have not been conducted. No clinically significant interactions are known or expected due to the high dilution of the active ingredients.

Concomitant use with other medications is not expected to affect the activity of this preparation. Always inform your healthcare provider about all products you are using.

Contraindications

  • Apnea or any other diagnosed sleep-related breathing disorder.
  • Unexpected daytime drowsiness or a history of suddenly falling asleep at inappropriate times.
  • Pregnancy at any trimester.
  • Use in pediatric patients under 18 years of age.
  • Known hypersensitivity to any component of the product, including lactose.

Overdose

Overdose is unlikely due to the homeopathic dilution of the active substances. No specific antidote exists.

In case of accidental ingestion of a significantly larger than recommended dose, monitor for general discomfort and allergic-type reactions. Provide symptomatic and supportive care. Contact a poison control center or physician if concerned.

Use in Pregnancy and Lactation

Contraindicated during pregnancy.

Pediatric Use

Contraindicated in children under 18 years of age.

Special Precautions

If there is no effect within a week, the drug should be discontinued.

Storage Conditions

At a temperature not exceeding 20°C (68°F). Keep out of reach of children.

Shelf Life

The shelf life is 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

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