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Medicine in DR Congo · official US FDA label

Diarasol 2 mg

Loperamide (loperamide) · comprimé

Authorized in DR Congo

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This is a US label.

The official US FDA label for loperamide (published as LOPERAMIDE HYDROCHLORIDE), effective September 9, 2026, describes products sold in the United States. The medicine sold in DR Congo may differ in strength, form or approved uses: ask a pharmacist or a doctor.

Official US FDA label for loperamide

Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. The full label on DailyMed.

Uses

Use controls symptoms of diarrhea, including Travelers' Diarrhea

Dosage

US dosage, for products sold in the United States. For a medicine bought in DR Congo, follow its box, its leaflet or your pharmacist.

Directions drink plenty of clear fluids to help prevent dehydration caused by diarrhea. not for use in children under 12 years of age adults and children 12 years and over: 2 softgels after the first loose stool; 1 softgel after each subsequent loose stool; but no more than 4 softgels in 24 hours

Warnings and precautions

Warnings Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide hydrochloride Heart alert: Taking more than directed can cause serious heart problems or death

Where to find it in DR Congo

Not in stock in our pharmacies right now

Stock changes with every sale. Search by substance: a medicine with the same composition may be available.

Composition

SubstanceStrengthATC code
CHLORHYDRATE DE LOPÉRAMIDE (loperamide)2 mg—

Marketing authorization in DR Congo

From the register of the ACOREP (the Congolese pharmaceutical regulatory authority).

  • Authorization number

    ACRP/CAB/DG/D11/00/C/MH/2078/2025

    Valid from March 24, 2025 until March 24, 2030

    Holder
    LEMON PHARMA, BAS CONGO, N°19, C/GOMBE, KINSHASA – RDC
    Manufacturer
    SANTE BIOTECH PRIVATE LIMITED 256-257, Sector-I, Pithampur, Dist – Dhar (M.P) - 454775
    Country
    Inde

Sources

  • ●Labels: U.S. Food and Drug Administration, openFDA (public domain). Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. DailyMed.
  • ●English names of substances: RxNorm, U.S. National Library of Medicine.
  • ●Marketing authorizations: register of the ACOREP, DR Congo, version of February 4, 2026.

Public information, for reference only: it does not replace the advice of a pharmacist or a doctor. Vimpia writes nothing about how to use a medicine and translates nothing: the label is the US FDA's, unchanged; names, composition and authorizations come from the official sources above.