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Medicine in DR Congo · official US FDA label

LANOCARE CREME 30 g

Lanoline (lanolin) · crème topique

Authorized in DR Congo

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This is a US label.

The official US FDA label for lanolin, effective August 19, 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 lanolin

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

Uses

Uses Temporarily protects minor: cuts scrapes burns Temporarily protects and helps relieve chafed, chapped or cracked skin Helps protect from the drying effects of wind and cold weather. Directions Apply as needed

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.

Apply as needed

Warnings and precautions

For external use only. When using this product do not get into eyes. Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days Do not use on deep or puncture wounds animal bites serious burns

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
Lanoline (lanolin)30 g—

Marketing authorization in DR Congo

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

  • Authorization number

    ACRP/CAB/DG/D11/00/A/MH/2423/2025

    Valid from May 27, 2025 until May 27, 2030

    Holder
    NEW CESAMEXSARL AV. Général Bobazo7155, Kingabwa- Limete Kinshasa-R.D.Congo
    Manufacturer
    AURA LIFECARE PVT. LTD S. No. 254/14/1, Jarod-Savli Road, P.O. Karachiya-391 520, Tal. Savli, Dist. Vadodara, 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.