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Fiches Amavita / Sun Store / Coop Vitality
Details
- Product number
- 3807601
- CPT
- -
- Packaging group
- 100
- Unit
- Dragée(s)
- Composition
- bisacodylum 5 mg, lactosum monohydricum 27.2 mg, solani amylum, acaciae gummi, gelatina, talcum, silica colloidalis anhydrica, magnesii stearas, Überzug: saccharum 29.784 mg, E 218 0.027 mg, gelatina, acaciae gummi, acidi methacrylici et methylis methacrylatis polymerisatum 1:2, calcii carbonas, silica colloidalis hydrica, talcum, silica colloidalis anhydrica, E 104, E 127, cera carnauba, cera flava, lacca, pro compresso obducto.
Articles (1)
Prontolax, Dragées
Dragées
100
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
bisacodylum
|
5.0 MG | Substance | Wirkstoff (Principe actif) |
|
lactosum monohydricum
|
27.2 MG | Substance | HBESI |
|
solani amylum
|
- | Substance | HNIDK |
|
acaciae gummi
|
- | Substance | HNIDK |
|
gelatina
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
magnesii stearas
|
- | Substance | HNIDK |
|
saccharum
|
29.784 MG | Substance | HBESI |
|
E 218
|
0.027 MG | Substance | HBESI |
|
gelatina
|
- | Substance | HNIDK |
|
acaciae gummi
|
- | Substance | HNIDK |
|
acidi methacrylici et methylis methacrylatis polymerisatum 1:2
|
- | Substance | HNIDK |
|
calcii carbonas
|
- | Substance | HNIDK |
|
silica colloidalis hydrica
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
E 104
|
- | Substance | FIMDK |
|
E 127
|
- | Substance | FIMDK |
|
cera carnauba
|
- | Substance | HNIDK |
|
cera flava
|
- | Substance | HNIDK |
|
lacca
|
- | Substance | HNIDK |
Authorization holder
Streuli Pharma AG
8730 Uznach
Authorization information
- Swissmedic authorization number
- 38076
- Drug name
- Prontolax, Dragées
- Galenic form
- UEBT
- ATC Code
- A06AB02
- Authorization status
- Z
- Dispensation category
- B/D
- First authorization
- 21/05/1975
- Authorization expiration date
- 31/12/9999
- IT number
- 04.08.11
- Domain
- Human medicine
Packaging details
- Description (FR)
- PRONTOLAX drag 5 mg 100 pce
- Description (DE)
- PRONTOLAX Drag 5 mg 100 Stk
- Market launch
- 21/05/1975
- Narcotic (BTM)
- No