- Product NDC
- 69607-0007
- 11-digit product format
- 696070007
- Labeler code
- 69607
- Product ID
- 69607-0007_f47eee26-e648-4cc8-8f03-d47d9b031458
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimonium Tartaricum, Arsenicum Iodatum, Asafoetida, Baptisia Tinctoria, Echinacea (Angustifolia), Eupatorium Perfoliatum, Euphorbia Pilulifera, Hepar Sulphuris Calcareum, Kali Bichromicum, Kreosotum, Lachesis Mutus, Mercurius Iodatus Ruber, Pyrogenium, Silicea, Teucrium Marum
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Biovea
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-08-19
- Marketing end
- 2021-03-18
- Substance
- ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIIODIDE; ASAFETIDA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA HIRTA FLOWERING TOP; CALCIUM SULFIDE; POTASSIUM DICHROMATE; WOOD CREOSOTE; LACHESIS MUTA VENOM; MERCURIC IODIDE; RANCID BEEF; SILICON DIOXIDE; TEUCRIUM MARUM
- Active strength
- 6 [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record