Land: Vereinigte Staaten
Sprache: Englisch
Quelle: NLM (National Library of Medicine)
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD), AMMONIUM BROMIDE (UNII: R0JB3224WS) (BROMIDE ION - UNII:952902IX06), CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (CITRULLUS COLOCYNTHIS FRUIT PULP - UNII:23H32AOH17), ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I), GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q), MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY83
MediNatura Inc
ACONITUM NAPELLUS
ACONITUM NAPELLUS 6 [hp_X] in 1.1 mL
INTRADERMAL
PRESCRIPTION DRUG
Spascupreel® Injection Solution is contraindicated in patients with known hypersensitivity to Spascupreel® or any of its ingredients.
unapproved homeopathic
SPASCUPREEL- ACONITUM NAPELLUS, AMMONIUM BROMIDE, CITRULLUS COLOCYNTHIS FRUIT PULP, ATROPINE SULFATE, GELSEMIUM SEMPERVIRENS ROOT, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, VERATRUM ALBUM ROOT, PASSIFLORA INCARNATA FLOWERING TOP, MATRICARIA RECUTITA, AMANITA MUSCARIA FRUITING BODY AND CUPRIC SULFATE INJECTION MEDINATURA INC _Disclaimer: This homeopathic product has not been evaluated by the Food and Drug_ _Administration for safety or efficacy. FDA is not aware of scientific evidence to support_ _homeopathy as effective._ ---------- SPASCUPREEL 1.1ML INJECTION DESCRIPTION Each 1.1 ml solution for injection ampule contains: ACTIVE INGREDIENTS: INGREDIENT NAME POTENCY QUANTITY FINAL DILUTION Aconitum napellus 6X 2.20 µl 8.69X Agaricus muscarius 4X 0.55 µl 7.30X Ammonium bromatum 4X 1.10 µl 7.00X Atropinum sulphuricum 6X 1.10 µl 8.99X Chamomilla 3X 0.55 µl 6.30X Colocynthis 4X 1.10 µl 7.00X Cuprum sulphuricum 6X 0.55 µl 9.30X Gelsemium sempervirens 6x 1.10 µl 8.99X Magnesia phosphorica 6X 1.10 µl 8.99X Passiflora incarnata 2X 0.55 µl 5.30X Veratrum album 6X 1.10 µl 8.99X INACTIVE INGREDIENTS: Water for injection 1,089.0 μl Sodium Chloride 10.4 μl INDICATION AND USAGE Spascupreel® Injection Solution is a homeopathic drug product indicated for the relief of spasms of the smooth musculature of the gastrointestinal and the urogenital tract as well as general muscle spasms. DOSAGE AND ADMINISTRATION GENERAL CONSIDERATIONS The dosage schedules listed below can be used as a general guide for the administration of Spascupreel® Injection Solution. Spascupreel® Injection Solution may be administered s.c., i.d., i.m., or i.v. If co-administration with a local anesthetic is desired, Spascupreel Injection Solution may be mixed with lidocaine or similar agents at the discretion of the physician. The interval between injections is left to the discretion of the HCP, but should not exceed 1 ampule in 24 hours. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to admin Lesen Sie das vollständige Dokument