- Product NDC
- 50114-7040
- 11-digit product format
- 501147040
- Labeler code
- 50114
- Product ID
- 50114-7040_72a712a7-7d1f-436c-8f18-ddbc97047ce4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- 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
- Dosage form
- INJECTION
- Route
- INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- MediNatura Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-30
- Marketing end
- 2023-11-30
- Substance
- 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; CUPRIC SULFATE
- Active strength
- 6 [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record