Sudocrem cream for external use jar 60 g

Instructions Sudocrem cream for external use jar 60 g

Composition

active ingredients: 1 g of cream contains zinc oxide 15.25%, benzyl alcohol 0.39%, benzyl benzoate 1.01%, benzyl cinnamate 0.15%;

excipients: lanolin, purified water, sodium benzoate (E 211), paraffin wax, synthetic beeswax, microcrystalline wax, sorbitan sesquioleate, propylene glycol, linalyl acetate, lavender flavor, mineral oil, antioxidant containing: propylene glycol, anhydrous citric acid, butylhydroxyanisole (E 320).

Dosage form

Cream for external use.

Main physicochemical properties: white, homogeneous cream, without visible impurities, with a lavender scent.

Pharmacotherapeutic group

Dermatological preparations. Preparations with emollient and protective effects. Zinc preparations. ATX code D02A B.

Pharmacological properties

Pharmacodynamics.

Zinc oxide has an antiseptic, astringent, and anti-inflammatory effect. When applied to the skin, it relieves irritation and heals minor burns and shallow wounds.

Benzyl alcohol has a local anesthetic effect with disinfectant properties.

Benzyl benzoate has an antiseptic effect and also acts as a solvent.

Benzyl cinnamate is a synthesized substance from benzyl alcohol and cinnamic acid that has antibacterial and antifungal effects.

Indication

For local treatment:

- diaper dermatitis;

- diaper rash;

- minor thermal burns;

- frostbite of the 1st degree;

- acne;

- bedsores;

- eczema.

Contraindication

Hypersensitivity to any of the components of the drug. Acute purulent-inflammatory skin diseases.

Interaction with other medicinal products and other types of interactions

Unknown.

Application features

For external use only. Avoid contact with eyes and mucous membranes.

If it gets into the eyes or mucous membranes, they must be rinsed with water.

If the condition does not improve after using the cream, or even worsens, you should consult a doctor.

Use during pregnancy and breastfeeding

There are no contraindications. Can be used during pregnancy or breastfeeding after consulting a doctor.

Ability to influence reaction speed when driving vehicles or other mechanisms

Not installed.

Method of administration and doses

For external use only.

Unless otherwise prescribed, apply to adults and children no more than 6 times a day.

The drug should be applied in a thin layer to the affected areas of the skin.

The duration of treatment depends on the severity and course of the disease and is determined individually by the doctor.

If the condition does not improve after using the drug, or even worsens, you should consult a doctor.

Children

The drug can be used in pediatric practice.

Overdose

Overdose is unlikely with topical application. Accidental ingestion of large doses may cause vomiting, diarrhea, central nervous system stimulation, and convulsions.

Treatment is symptomatic.

Adverse reactions

Hypersensitivity reactions may rarely occur, including itching, flushing, rashes, changes at the site of application of the cream; excipients included in the medicinal product may cause skin irritation and local skin reactions (e.g. contact dermatitis).

Expiration date

3 years.

Storage conditions

Store at a temperature not exceeding 25 °C out of the reach of children.

Packaging

10 g or 15 g in a polypropylene jar; 1 polypropylene jar in a blister card. 60 g or 125 g or 250 g in a polypropylene jar with tamper-evident opening.

Vacation category

Without a prescription.

Producer

Forest Tosara Limited, Ireland.

Location of the manufacturer and its business address

Unit 146 Baldoyle Industrial Estate, Baldoyle, Dublin 13, Ireland.