- Product NDC
- 72250-0001
- 11-digit product format
- 722500001
- Labeler code
- 72250
- Product ID
- 72250-0001_c5e682fd-dce8-446d-9198-36799f82b4e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fucus Vesiculosus, Agnus Castus, Chelidonium Majus, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Phytolacca Decandra, Kali Phosphoricum, Magnesia Phosphorica, Carbo Vegetabilis, Graphites, Calcarea Carbonica, Natrum Phosphoricum, Hypophysis Suis, Placenta Totalis Suis, Thyroidinum (Suis)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BodyLogicMD of Fort Lauderdale
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-05-31
- Substance
- ACTIVATED CHARCOAL; CHASTE TREE; CHELIDONIUM MAJUS; DIBASIC POTASSIUM PHOSPHATE; FUCUS VESICULOSUS; GRAPHITE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND; SUS SCROFA PLACENTA; SUS SCROFA THYROID
- Active strength
- 10; 6; 6; 8; 4; 10; 6; 8; 12; 6; 6; 12; 6; 12; 12; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes