NUROFEN Dolo drag 200 mg 20 pce
7680502430029
CH-50243
M01AE01
07.10.1.
Active substances:
Fiches Amavita / Sun Store / Coop Vitality
Details
- Product number
- 5024301
- CPT
- -
- Packaging group
- 20
- Unit
- Dragée(s)
- Composition
- ibuprofenum 200 mg, carmellosum natricum conexum, natrii laurilsulfas, natrii citras dihydricus, acidum stearicum, silica colloidalis anhydrica, Überzug: carmellosum natricum, talcum, acaciae gummi dispersione desiccatum, saccharum 116.1 mg, macrogolum 6000, E 171, Drucktinte: lacca, E 172 (nigrum), propylenglycolum, pro compresso obducto corresp. natrium 12.65 mg.
Articles (1)
Nurofen Dolo, Dragées
Dragées
20
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
ibuprofenum
|
200.0 MG | Substance | Wirkstoff (Principe actif) |
|
carmellosum natricum conexum
|
- | Substance | HNIDK |
|
natrii laurilsulfas
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
natrii citras dihydricus
|
- | Substance | HNIDK |
|
acidum stearicum
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
carmellosum natricum
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
acaciae gummi dispersione desiccatum
|
- | Substance | HNIDK |
|
saccharum
|
116.1 MG | Substance | HBESI |
|
macrogolum 6000
|
- | Substance | HNIDK |
|
E 171
|
- | Substance | FNIDK |
|
lacca
|
- | Substance | HNIDK |
|
E 172 (nigrum)
|
- | Substance | FTODK |
|
propylenglycolum
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
natrium
|
12.65 MG | Substance | HBESI |
Authorization holder
Reckitt Benckiser (Switzerland) AG
8304 Wallisellen
Authorization information
- Swissmedic authorization number
- 50243
- Drug name
- Nurofen Dolo, Dragées
- Galenic form
- DRAG
- ATC Code
- M01AE01
- Authorization status
- Z
- Dispensation category
- D
- First authorization
- 29/01/1991
- Authorization expiration date
- 31/12/9999
- IT number
- 07.10.1.
- Domain
- Human medicine
Packaging details
- Description (FR)
- NUROFEN Dolo drag 200 mg 20 pce
- Description (DE)
- NUROFEN Dolo Drag 200 mg 20 Stk
- Market launch
- 29/01/1991
- Narcotic (BTM)
- No