Dentinox N 10g

Dentinox N gel can be used in the case of gingivitis. Recommended for infants and children with baby teeth.Its local active ingredients anesthetize the gums.

Symptoms

It is a traditional medicine for topical application to the gums. It is a combined preparation containing ingredients with a pain-reducing and anti-inflammatory effect. The effectiveness of the product in the above-mentioned indications is based solely on long-term use and experience.

Dentinox N is a mildly-acting preparation used for a short time in the treatment of acute pain and gingivitis related to the eruption of deciduous teeth and molars.

Active substance: Chamomillae tinctura, Lidocainum, Macrogoli aether laurilicus

Composition

10 g of gel contains:	chamomillae tinctura (chamomile tincture) (1: 4-4.5) 1500 mg,
	ethanol extractant 70% (V / V),
	lidocaine hydrochloridum (lidocaine hydrochloride) 34 mg,
	macrogoli aether laurilicum (macrogol lauryl ether) 32 mg,
	ethanol content in the product max 9.5%,
	excipients with known effect: propylene glycol 1500 mg, non-crystallising liquid sorbitol 1000 mg.

Dosage

Use short-term in case of acute symptoms of teething.

Method of administration:

Gingival application. Lubricate the gums with a small amount of gel (the size of a pea) using a clean finger or a cotton swab and rub in lightly. This activity should be repeated 2-3 times a day, especially after eating or after performing oral hygiene before going to bed. If after 7 days there is no improvement or the patient feels worse, you should see your doctor. Dentinox N should be used after eating.

Contraindications

• Hypersensitivity to the active substances or to any of the excipients.
• Intolerance to chamomile or other Asteraceae plants, lidocaine or similar local anesthetics (amide type).
• Hypersensitivity reactions to chamomile (e.g. contact dermatitis) are very rare. Cross-reaction may occur in people allergic to plants of the Asteraceae family (e.g. mugwort).
• Due to the content of sorbitol, the drug should not be used by patients suffering from rare hereditary fructose intolerance.
• Dentinox N should not be used in infants under 3 months of age.
• Dentinox N should also not be used in infants under 12 months of age who are simultaneously treated with agents causing methaemoglobinaemia.

Contents

Due to the content of the herbal active substance (Chamomillae tinctura), Dentinox N gel has a light brown color.

The package includes an aluminum tube with a polyethylene screw cap containing 10 g of gel, packed with the patient information leaflet in a cardboard box.

Storage method

15°C-25°C

Manufacturer

DENTINOX

Warnings

Talk to your doctor or pharmacist before using Dentinox N

• Avoid contact with the eyes. In the event of accidental eye contact, rinse eyes with plenty of water or saline.
• Contact your doctor if you experience more redness or swelling of the gums or if you experience hypersensitivity reactions on the skin or mucous membranes. The same applies to the occurrence of secondary accompanying ailments.
• Caution should be exercised in patients with congenital or acquired methaemoglobinaemia or in patients with glucose-6-phosphate dehydrogenase deficiency due to an increased risk of drug-induced methaemoglobinaemia.
• Dentinox N contains propylene glycol and sorbitol. Due to the content of propylene glycol, local irritation may occur when Dentinox N is applied to the oral mucosa.
• The drug contains sorbitol, therefore it should not be used by patients suffering from rare hereditary fructose intolerance. If you have been diagnosed with an intolerance to some sugars, please contact your doctor.

10 g of gel contains: 1 g of sorbitol (corresponding to 0.25 g of fructose), i.e. less than 0.1 bread unit. Caloric value: 2.6 kcal / g sorbitol. The drug contains small amounts of ethanol (alcohol), less than 100 mg per dose.

Side effect

Allergic reactions may occur, especially related to the lidocaine content.