Chelidonium comp. Gocce per uso orale
Ülke: İsviçre
Dil: İtalyanca
Kaynak: Swissmedic (Swiss Agency for Therapeutic Products)
Bilgilendirme broşürü
(PIL)
15-05-2024
Ürün özellikleri
(SPC)
15-05-2024
Aktif bileşen:
silybum marianum, ethanol. decoctum (HAB) D1, chelidonium majus (HAB) TM, onopordum acanthium e folium TM (Ph.Eur.Hom. 1.1.7), taraxacum officinale (HAB) TM, urtica dioica (Ph.Eur.Hom.) TM (Ph.Eur.Hom. 1.1.4), dryopteris filix-mas herba rec. (Dryopteris filix-mas (L.) SCHOTT), polypodium vulgare herba rec. (Polypodium vulgare L.), phyllitis scolopendrium herba rec. (Asplenium scolopendrium L.), salix alba folium rec. (Salix alba L.), salix vitellina folium rec. (Salix alba ssp. vitellina (L.) ARCANG), salix viminalis folium rec. (Salix viminalis L.)
Mevcut itibaren:
Weleda AG
INN (International Adı):
silybum marianum, ethanol. decoctum (HAB) D1, chelidonium majus (HAB) TM, onopordum acanthium e folium TM (Ph.Eur.Hom. 1.1.7), taraxacum officinale (HAB) TM, urtica dioica (Ph.Eur.Hom.) TM (Ph.Eur.Hom. 1.1.4), dryopteris filix-mas herba rec. (Dryopteris filix-mas (L.) SCHOTT), polypodium vulgare herba rec. (Polypodium vulgare L.), phyllitis scolopendrium herba rec. (Asplenium scolopendrium L.), salix alba folium rec. (Salix alba L.), salix vitellina folium rec. (Salix alba ssp. vitellina (L.) ARCANG), salix viminalis folium rec. (Salix viminalis L.)
Farmasötik formu:
Gocce per uso orale
Kompozisyon:
silybum marianum, ethanol. decoctum (HAB) D1 167 mg, chelidonium majus (HAB) TM 50 mg, onopordum acanthium e folium TM (Ph.Eur.Hom. 1.1.7) 56 mg, taraxacum officinale (HAB) TM 33 mg, urtica dioica (Ph.Eur.Hom.) TM (Ph.Eur.Hom. 1.1.4) 33 mg, digestio ethanolica 30 mg ex dryopteris filix-mas herba rec. (Dryopteris filix-mas (L.) SCHOTT) 8 mg, ratio: 1:3,1, Auszugsmittel ethanolum 25% (m/m), digestio ethanolica 6.7 mg ex polypodium vulgare herba rec. (Polypodium vulgare L.) 2 mg, ratio: 1:3,1, Auszugsmittel ethanolum 25% (m/m), digestio ethanolica 30 mg ex Phyllitis scolopendrium herba rec. (Asplenium scolopendrium L.) 8 mg, ratio: 1:3,1, Auszugsmittel ethanolum 25% (m/m), digestio ethanolica 17 mg ex salix alba folium rec. (Salix alba L.) 4 mg, ratio: 1:3,1, Auszugsmittel ethanolum 25% (m/m), digestio ethanolica 17 mg ex salix vitellina folium rec. (Salix alba ssp. vitellina (L.) ARCANG) 4 mg, ratio: 1:3,1, Auszugsmittel, digestio ethanolica 33 mg ex salix viminalis folium rec. (Salix viminalis L.) 8 mg, ratio: 1:3,1, Auszugsmittel ethanolum 25% (m/m), ethanolum 96 per centum 161 mg, aqua purificata, saccharum 33 mg, ad solutionem pro 1 g, corresp. 27 guttae, corresp. ethanolum 45 % V/V.
Sınıf:
D
Terapötik grubu:
Antroposofici
Terapötik alanı:
Zulassung mit reduziertem Dossier ohne Indikation nach Art. 25 Abs. 1 KPAV (SR 812.212.24)
Yetkilendirme durumu:
zugelassen
Yetkilendirme tarihi:
2015-06-16
