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Substance · official US FDA label

Glycérine (glycerin)

1 medicine listed on Vimpia contains it, alone or combined. Below, the official US FDA label for glycerin, unchanged.

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This is a US label.

The official US FDA label for glycerin, effective September 8, 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 glycerin

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

Uses

1. Wash and dry the affected area. 2. Apply two coats using the included fiber brush. 3. Wait for the skin to absorb the liquid. 4. Apply 2 times daily morning and night.

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.

1. Wash and dry the affected area. 2. Apply two coats using the included fiber brush. 3. Wait for the skin to absorb the liquid. 4. Apply 2 times daily morning and night.

Warnings and precautions

Warnings Please keep out of reach of children. Do not swallow. Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

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.