Halmanin-MFF (Powder) Instructions for Use

Marketing Authorization Holder

Moscow Pharmaceutical Factory CJS (Russia)

ATC Code

D08AX (Other antiseptics and disinfectants)

Active Substances

Salicylic acid (USP United States Pharmacopeia)

Zinc oxide (Ph.Eur. European Pharmacopoeia)

Dosage Form

Halmanin-MFF

Powder for external use 2 g+10 g/100 g: 20 g or 30 g jars 1 pc., 2 g sachets 5 or 10 pcs.

Dosage Form, Packaging, and Composition

Excipients : talc 44 g, potato starch 44 g.

20 g – plastic jars (1) – cardboard packs.
30 g – plastic jars (1) – cardboard packs.
2 g – heat-sealed sachets (5) – cardboard packs.
2 g – heat-sealed sachets (10) – cardboard packs.

The shelf life of the drug in sachets is 2 years, in jars – 5 years.

Clinical-Pharmacological Group

Drug with antimicrobial and drying action for external use

Pharmacotherapeutic Group

Antiseptic

Pharmacological Action

The drug has an absorbent, drying, and astringent effect.

Indications

• Foot sweating.

ICD codes

Dosage Regimen

Apply externally only as a powder.

Use once daily on clean, thoroughly dry skin.

Apply a thin, even layer to the affected areas, such as the feet.

Ensure the skin is completely dry before application to maximize the absorbent and drying effects.

Avoid application to broken skin, open wounds, or mucous membranes.

Do not apply to inflamed or bleeding skin surfaces.

Discontinue use and consult a physician if severe irritation or signs of a hypersensitivity reaction occur.

Do not use in children under 12 years of age.

For external use only. Avoid contact with eyes.

Adverse Reactions

Adverse reactions are uncommon.

Itching and localized skin irritation may occur rarely.

Discontinue use immediately and consult a physician if signs of a hypersensitivity reaction develop.

Drug Interactions

No specific drug interactions are known.

Avoid concurrent use with other topical medications applied to the same area without medical advice.

Consult a physician before using with other drying or astringent agents.

Contraindications

• Hypersensitivity to salicylic acid, zinc oxide, talc, potato starch, or any other component of the formulation.
• Use in children under 12 years of age.
• Application to inflamed, broken, or bleeding skin.

Overdose

Systemic absorption and overdose from topical use are unlikely.

Excessive application may lead to increased local skin dryness, irritation, or peeling.

In case of accidental ingestion, seek immediate medical attention and show the package leaflet or label to the physician.

Pediatric Use

Contraindicated in children under 12 years of age.

Storage Conditions

At a temperature not exceeding 25°C (77°F), in a dry place and out of the reach of children.

Shelf Life

Shelf life – 5 years in plastic jars; 2 years in heat-sealed sachets.

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.