AKNICHTHOL susp fl 30 g

7680330050413 CH-33005 D10AX30 10.02.0.
AKNICHTHOL susp fl 30 g
AKNICHTHOL susp fl 30 g
AKNICHTHOL susp fl 30 g
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Details

Product number
3300501
CPT
-
Packaging group
30
Unit
g
Composition
natrii bituminosulfonas decoloratus 10 mg, acidum salicylicum 5 mg, alcohol isopropylicus, macrogoli 4 aether laurilicus, maydis amylum, E 171, silica colloidalis anhydrica, triglycerida media, E 172 (flavum), E 172 (rubrum), E 172 (nigrum), aqua purificata q.s. ad suspensionem pro 1 g.

Articles (1)

Aknichthol, Suspension
suspension
30
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Professional SmPC
Allemand
06/04/2023
Professional SmPC
Français
06/04/2023
Professional SmPC
Italien
06/04/2023
Patient information leaflet
Allemand
31/03/2023
Patient information leaflet
Français
31/03/2023
Patient information leaflet
Italien
31/03/2023

Detailed composition

Substance Quantity Type Category
(N/A)
10.0 MG Substance Wirkstoff (Principe actif)
(N/A)
5.0 MG Substance Wirkstoff (Principe actif)
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance FNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance FTODK
(N/A)
- Substance FTODK
(N/A)
- Substance FTODK
(N/A)
- Substance HNIDK

Authorization holder

Merz Pharma (Schweiz) AG

4123 Allschwil

Authorization information

Swissmedic authorization number
33005
Drug name
Aknichthol, Suspension
Galenic form
SUKU
ATC Code
D10AX30
Authorization status
Z
Dispensation category
D
First authorization
11/09/1967
Authorization expiration date
31/12/9999
IT number
10.02.0.
Domain
Human medicine
Field of application
Akne vulgaris

Packaging details

Description (FR)
AKNICHTHOL susp fl 30 g
Description (DE)
AKNICHTHOL Susp Fl 30 g
Market launch
11/09/1967
Narcotic (BTM)
No

Other packaging sizes