- Product NDC
- 58264-0353
- 11-digit product format
- 582640353
- Labeler code
- 58264
- Product ID
- 58264-0353_2b530979-bfa9-24b5-e063-6394a90a76eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SILVER, CALCIUM IODIDE, LYTTA VESICATORIA, COPPER, FERROUS IODIDE, GOLDENSEAL, IODINE, DAPHNE MEZEREUM BARK, PHOSPHORIC ACID, Phosphorus, TOXICODENDRON PUBESCENS LEAF, and RUMEX CRISPUS WHOLE
- Dosage form
- SOLUTION
- Route
- SUBLINGUAL
- Labeler
- DNA Labs, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1990-01-01
- Substance
- CALCIUM IODIDE; COPPER; DAPHNE MEZEREUM BARK; FERROUS IODIDE; GOLDENSEAL; IODINE; LYTTA VESICATORIA; PHOSPHORIC ACID; PHOSPHORUS; RUMEX CRISPUS WHOLE; SILVER; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 8; 12; 30; 8; 6; 6; 6; 6; 30; 6; 12; 6 [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
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Inhibit Ovum Fertilization [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes