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Substance · official US FDA label

Pramocaïne (pramoxine)

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

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This is a US label.

The official US FDA label for pramoxine (published as PRAMOXINE HYDROCHLORIDE), effective June 23, 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 pramoxine

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

Uses

Uses temporarily relieves itching and irritation of the external genital area.

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 wash hands before and after applying • adults and children 12 years of age and older: wet the external genital area, apply a small amount, leave on briefly, then rinse thoroughly and pat dry • use once or twice daily, or as needed • do not use inside the vagina • children under 12 years of age: ask a doctor

Warnings and precautions

Warnings For external use only Do not use • internally or inside the vagina • in or around the eyes When using this product • avoid contact with the eyes and mucous membranes • do not apply to open wounds or broken skin Stop use and ask a doctor if • condition worsens • redness or irritation increases • symptoms persist for more than 7 days, or clear up and occur again within a few days If pregnant or breast-feeding , ask a health professional before use. 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.

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.