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Medicines in DR CongoVersion française

Substance · official US FDA label

Biotine (biotin)

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

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This is a US label.

The official US FDA label for biotin, effective July 3, 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 biotin

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

Uses

INDICATIONS & USAGE SECTION Uses: Helps moisturize dry scalp and hair. Helps improve the appearance of dry, brittle and frizzy hair. Helps reduce the appearance of hair breakage caused by dryness.

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 Directions: Apply a proper amount to scalp and hair. Massage gently until absorbed. Use as needed.

Warnings and precautions

Warnings Warnings: For external use only. Avoid contact with eyes and sensitive skin areas. Do not use on broken or irritated skin. Discontinue use if irritation occurs. Keep out of reach of children.

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.