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Medicine in DR Congo · official US FDA label

Ketin 2% p/p

Kétoconazole (ketoconazole) · crème topique

Authorized in DR Congo

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This is a US label.

The official US FDA label for ketoconazole, effective September 5, 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 ketoconazole

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

Uses

For best results, follow these steps carefully:lukewarm water. 1.Wet hair and scalp thoroughly with 2.Applya sufficient amount of shampooto generate a rich lather.3.Gently massage the lather into your scalp and hair. 4.Leave the lather on the scalp for 3-5medication to work effectively.5.Rinse thoroughly with water. minutes. This contact time is crucialfor the

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.

Use every 3-4 days for up to 8 weeks. Afterthat, use only asneeded to control dandruff.

Warnings and precautions

For external use only. Avoid contact witheyes. Ifcontact occurs, rinse thoroughlywithwater.

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
Kétoconazole (ketoconazole)2% p/p—

Marketing authorization in DR Congo

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

  • Authorization number

    MS/1253/10/05/DGM/915/2022

    Valid from July 26, 2022 until July 26, 2027

    Holder
    INDAPHAR 92 Av. Bas-Congo n° 30, commune de Gombe, ville de Kinshasa, R.D Congo
    Manufacturer
    Accretion Pharmaceuticals 28/29, Xcelon Industrial Park-1, Behind Intas Pharmaceuticals Vasna- Chacharwadi, Ta- Sanand, Dist. : Ahmedabad 382213, Gujarat, India
    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.