Medicine · official US FDA label
SELENIUM PANPHARMA 100 microgrammes
Sélénium (selenium) · solution injectable
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Not in stock in our pharmacies right now. Trouver shows when it is back near you. The reservation pages are in French.
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.
Prescription medicine: follow the dose prescribed by your 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
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
| Substance | Strength | ATC code |
|---|---|---|
| SÉLÉNIUM (selenium) | 100 microgrammes / une ampoule de 2 mL | — |
| SÉLÉNITE DE SODIUM PENTAHYDRATÉ | 0,333 microgrammes / une ampoule de 2 mL | — |
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.
- ●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.