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Medicine in DR Congo · official US FDA label

Argenex Gel Ionic 0.2%

Nitrate d'argent (silver nitrate) · crème topique

Authorized in DR Congo

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This is a US label.

The official US FDA label for silver nitrate, effective December 10, 2025, 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 silver nitrate

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

Uses

For cleansing and removing bacteria in the intimate 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: Gently wipe intimate areas from front to back as needed or before intercourse. DO NOT FLUISH Reseal pouch after use to retain moisture. For external use only.

Warnings and precautions

For external use only. Flammable.

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

SubstanceStrengthATC code
NITRATE D'ARGENT (silver nitrate)0.2%—

Marketing authorization in DR Congo

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

  • Authorization number

    MS1253/10/05/251/2022

    Valid from February 8, 2022 until February 8, 2027

    Holder
    CROWN Av. Mwepu n° 2, Commune de Lubumbashi, Ville de Lubumbashi, Haut- Katanga, R.D Congo
    Manufacturer
    Alicon Pharmaceutical Pvt. Ltd.Plot. N°1919, G.I.D.C, Sarigam, Dist. § Valsad, Gujarat 396155 / 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.