Substance · official US FDA label
Phosphate d'aluminium (aluminum)
2 medicines listed on Vimpia contain it, alone or combined. Below, the official US FDA label for aluminum, unchanged.
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This is a US label.
The official US FDA label for aluminum (published as ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY), effective September 21, 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 aluminum
Data provided by the U.S. Food and Drug Administration (openFDA), unchanged. The full label on DailyMed.
Uses
Use reduces underarm wetness
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 apply to underarms only
Warnings and precautions
Warnings For external use only. Do not use on broken skin Ask a doctor before use if you have kidney disease Stop use if rash or irritation occurs Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Medicines that contain it
Names as they are sold. A medicine without an English page links to its French page.
- MOXYDAR, suspension buvable en sachet (in French)
Combined with other substances
- REFLOXAR, suspension buvable en sachet (in French)
Combined with other substances
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.