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Dantinorm® Baby (Solution) Instructions for Use

Marketing Authorization Holder

Boiron (France)

Contact Information

BOIRON (France)

ATC Code

V30 (Not assigned)

Dosage Form

Bottle OTC Icon Dantinorm® Baby Homeopathic oral solution: containers 1 ml (1 dose) 10 or 30 pcs.

Dosage Form, Packaging, and Composition

Homeopathic oral solution transparent, colorless.

1 dose
Chamomilla vulgaris C9 333.3 mg
Phytolacca decandra C5 333.3 mg
Rheum C5 333.3 mg

Excipients: purified water – up to 1 ml.

1 dose (1 ml) – polyethylene containers (5) – sachets made of polyethylene and aluminum foil (2) – cardboard packs with a side-sealing “tab”.
1 dose (1 ml) – polyethylene containers (5) – sachets made of polyethylene and aluminum foil (6) – cardboard packs with a side-sealing “tab”.

Clinical-Pharmacological Group

A drug used to facilitate teething in children

Pharmacotherapeutic Group

Homeopathic agent

Pharmacological Action

A multicomponent homeopathic medicine, the action of which is due to the components that make up its composition.

Indications

  • Painful teething in children.

ICD codes

ICD-10 code Indication
K00.7 Teething syndrome
ICD-11 code Indication
DA07.60 Teething 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.

Administer orally. Use one single-dose container (1 ml) two to three times per day. Administer between meals.

Limit the duration of treatment to three days. If symptoms persist beyond this period, discontinue use and seek medical advice.

Open the sachet and separate one container. Open the container by twisting the head. With the child in a seated position, squeeze the container to release the solution into the child’s mouth. Discard the used container immediately. Reseal the sachet containing the remaining containers.

Adverse Reactions

No adverse reactions have been reported to date. Monitor the patient for any signs of intolerance.

Despite the favorable safety profile, the possibility of allergic reactions or idiosyncratic reactions cannot be entirely excluded. Report any suspected adverse reaction to a healthcare professional.

Contraindications

  • Hypersensitivity to any of the active substances (Chamomilla vulgaris, Phytolacca decandra, Rheum) or to any of the excipients.

Special Precautions

If there is no therapeutic effect within 3 days, you should consult a doctor.

The container should not be stored after opening. The container must be discarded immediately after use.

Overdose

No cases of overdose have been reported. Due to the nature and dilution of the active ingredients, toxic effects are not anticipated.

In the event of accidental ingestion of a significantly larger than recommended quantity, seek medical attention or contact a Poison Control Center. Provide symptomatic and supportive care as required.

Drug Interactions

The use of this homeopathic medicine does not preclude treatment with other medicinal products. No specific pharmacokinetic or pharmacodynamic interactions are known or expected.

Concurrent use with other medications is not a contraindication. However, always inform a healthcare provider about all products the patient is using.

Storage Conditions

The drug should be stored out of the reach of children at a temperature not exceeding 25°C (77°F).

Shelf Life

Shelf life – 3 years. Do not use after the expiration date.

Dispensing Status

The drug 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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