Aknilox 2%

Aknilox 2% is a medicine authorised by Swissmedic under authorisation number 51303. The authorisation holder is Drossapharm AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 11 January 1993 and the authorisation is valid without a time limit. ATC code D10AF02 places the medicine in the group Anti-acne preparations.

  • Dispensing category B
  • Authorisation number 51303
  • ATC D10AF02
  • Synthetic medicines
Authorisation data
Authorisation number51303
NameAknilox 2%
Full nameAknilox 2%, Gel
Authorisation holderDrossapharm AG
Medicinal product codeSynthetic medicines
Dispensing categoryB · Prescription only
ATC codeD10AF02
First authorisation11 January 1993
Authorisation validityunlimited
Strengths
No.NameDispensing categoryAuthorisation date
3Aknilox 2%, GelB03 September 2008
4Aknilox 4%, GelB03 September 2008

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Pack sizes
Pack codeQuantityUnitATCIT codeDispensing category
3230gD10AF0210.02.0.B
4030gD10AF0210.02.0.B

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Medicines in the same ATC group

Other medicines from this authorisation holder

Frequently asked questions

Is Aknilox 2% authorised in Switzerland?

Yes. Aknilox 2% is authorised by Swissmedic under authorisation number 51303, data as of 01 September 2026. The authorisation is valid without a time limit.

Which dispensing category does Aknilox 2% have?

Aknilox 2% is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.

Who is the authorisation holder of Aknilox 2%?

The authorisation holder is Drossapharm AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.

Sources

Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.

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