SIMILASAN Allergie solaire crème tb 50 g

7680516760181 CH-51676 20.01.1.
SIMILASAN Allergie solaire crème tb 50 g
SIMILASAN Allergie solaire crème tb 50 g
SIMILASAN Allergie solaire crème tb 50 g
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Details

Product number
5167601
CPT
-
Packaging group
50
Unit
g
Composition
fagopyrum esculentum (HAB) D6 30 mg, hypericum perforatum (HAB) D4 30 mg, hypericum perforatum (HAB) D6 20 mg, hypericum perforatum (HAB) D12 20 mg, aqua ad iniectabile, alcohol cetylicus 100 mg, arachidis oleum hydrogenatum 200 mg, polysorbatum 60 50 mg, propylenglycolum 200 mg, natrii chloroargentas, ad unguentum pro 1 g.

Articles (1)

Similasan Sonnenallergie, Creme
Creme
50
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
30/01/2024
Patient information leaflet
Français
30/01/2024
Patient information leaflet
Italien
30/01/2024

Detailed composition

Substance Quantity Type Category
(N/A)
30.0 MG Substance Wirkstoff (Principe actif)
(N/A)
30.0 MG Substance Wirkstoff (Principe actif)
(N/A)
20.0 MG Substance Wirkstoff (Principe actif)
(N/A)
20.0 MG Substance Wirkstoff (Principe actif)
(N/A)
- Substance HNIDK
(N/A)
100.0 MG Substance HBESI
(N/A)
200.0 MG Substance HBESI
(N/A)
50.0 MG Substance HBESI
(N/A)
200.0 MG Substance HBESI
(N/A)
- Substance Konservierungsstoff (Conservateur)

Authorization holder

Similasan AG

8916 Jonen

Authorization information

Swissmedic authorization number
51676
Drug name
Similasan Sonnenallergie, Creme
Galenic form
CREM
Authorization status
Z
Dispensation category
D
First authorization
26/05/1992
Authorization expiration date
31/12/9999
IT number
20.01.1.
Domain
Human medicine
Field of application
Gemäss homöopathischem Arzneimittelbild bei Sonnenallergie.

Packaging details

Description (FR)
SIMILASAN Allergie solaire crème tb 50 g
Description (DE)
SIMILASAN Sonnenallergie Creme Tb 50 g
Market launch
26/05/1992
Narcotic (BTM)
No

Other packaging sizes