- Product NDC
- 64578-0178
- 11-digit product format
- 645780178
- Labeler code
- 64578
- Product ID
- 64578-0178_39f96260-9523-d104-e063-6294a90a1c64
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aceticum acidum, Ammonium muriaticum, Argentum metallicum, Aurum metallicum, Calcarea fluorica, Calcarea phosphorica, Carbolicum acidum, Citrus limonum, Cuprum metallicum, Ferrum metallicum, Glycyrrhiza glabra, Lappa major, Medulla ossis suis, Mercurius solubilis, Myrrha, Natrum fluoratum, Palladium metallicum, Phosphoricum acidum, Phytolacca decandra, Selenium metallicum, Silicea, Stannum metallicum, Staphysagria, Stillingia sylvatica, Trifolium pratense, X-Ray, Zincum oxydatum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energetix Corporation
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-09-04
- Substance
- ACETIC ACID; AMMONIUM CHLORIDE; ARCTIUM LAPPA ROOT; CALCIUM FLUORIDE; COPPER; DELPHINIUM STAPHISAGRIA SEED; GLYCYRRHIZA GLABRA; GOLD; IRON; LACTOSE, X-RAY EXPOSED (1000 RAD); LEMON JUICE; MERCURIUS SOLUBILIS; MYRRH; PALLADIUM; PHENOL; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; SELENIUM; SILICON DIOXIDE; SILVER; SODIUM FLUORIDE; STILLINGIA SYLVATICA ROOT; SUS SCROFA BONE MARROW; TIN; TRIBASIC CALCIUM PHOSPHATE; TRIFOLIUM PRATENSE FLOWER; ZINC OXIDE
- Active strength
- 15; 15; 4; 12; 15; 6; 4; 15; 12; 30; 12; 12; 6; 15; 15; 15; 4; 15; 12; 15; 12; 4; 9; 15; 12; 4; 15 [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_C]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes