- Product NDC
- 44911-0726
- 11-digit product format
- 449110726
- Labeler code
- 44911
- Product ID
- 44911-0726_bae9f92a-054a-4696-8cd2-e2eeb5d73157
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Abrotanum (Artemisia Abrotanum), Aethusa Cynapium, Baptisia Tinctoria, Cicuta Virosa, Cuprum Metallicum, Mezereum, Bufo Rana, Lac Materna Humanum, Saccharum Officinale, Serotonin (Hydrochloride), Alumina, Calcarea Phosphorica, Candida Albicans, Carcinosin, Lac Caninum, Mercurius Solubilis, Natrum Muriaticum, Propionic Acid, Sulphur, Thuja Occidentalis, Formalinum, Morbillinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-12-26
- Substance
- AETHUSA CYNAPIUM WHOLE; ALUMINUM OXIDE; ARTEMISIA ABROTANUM FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BUFO BUFO CUTANEOUS GLAND; CANDIDA ALBICANS; CANIS LUPUS FAMILIARIS MILK; CICUTA VIROSA ROOT; COPPER; DAPHNE MEZEREUM BARK; FORMALDEHYDE SOLUTION; HUMAN BREAST TUMOR CELL; HUMAN MILK; MEASLES VIRUS; MERCURIUS SOLUBILIS; PROPIONIC ACID; SEROTONIN HYDROCHLORIDE; SODIUM CHLORIDE; SUCROSE; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; TRIBASIC CALCIUM PHOSPHATE
- Active strength
- 6; 12; 6; 6; 15; 12; 12; 12; 12; 12; 15; 12; 30; 15; 12; 12; 30; 12; 30; 12; 12; 12 [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- Pharmacologic classes
- Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Fungal Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Fungal Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes