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Ethanol (ethanol)Version française

Medicine in DR Congo · official US FDA label

Sepgerm

Ethanol (ethanol) · gel désinfectant pour mains

Authorized in DR Congo

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This is a US label.

The official US FDA label for ethanol, effective August 13, 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 ethanol

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

Uses

Uses Hand sanitizing to decrease bacteria on skin. No rinsing required.

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 Wet hands thoroughly with spray mist. Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles. Continue rubbing vigorously until hands are dry. No rinsing or toweling is required.

Warnings and precautions

Warnings For external use only. Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water. Flammable. Keep away from fire, flame or spark.

Where to find it in DR Congo

Not in stock in our pharmacies right now

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Composition

SubstanceStrengthATC code
Ethanol (ethanol)—

Marketing authorization in DR Congo

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

  • Authorization number

    MS.1253/10/05/DGM/1184A/2021

    Valid from October 12, 2021 until October 12, 2026

    Holder
    SANTE VIE Av. de l’Action n° 10, commune de Gombe, ville de Kinshasa, R.D Congo
    Manufacturer
    T & T Pharma Care Plot no 1 Devrishi CHS Panchpakhadi Thane West -400602 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.