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Medicines in DR CongoVersion française

Substance · official US FDA label

Sélénium (selenium)

5 medicines listed on Vimpia contain it, alone or combined. Below, the official US FDA label for selenium, unchanged.

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This is a US label.

The official US FDA label for selenium (published as SELENIUM SULFIDE SALICYLIC ACID), effective September 4, 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 selenium

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

Uses

Apply to affected areas one to fourimes daily or as directed by doctor Shake before use Apply 2 to 3 drops inargeted areas directly to wet or dryscalp. Gently massage in. Use more asneeded. Apply to skin, leave on for15-20 minutes, then rinse off.

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.

worsens or does not improve afterregular use of this product asdirected

Warnings and precautions

For external use onlyWhen using this product Avoid contactwith eyes. If contact occurs, rinse eyesthoroughly with water

Medicines that contain it

Names as they are sold. A medicine without an English page links to its French page.

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.
  • ●Essential medicines: national list of essential medicines of DR Congo (LNME).
  • ●Composition: public medicines database of France (BDPM), ANSM, open licence.

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.