- Product NDC
- 69607-0008
- Requested package NDC
- 69607-0008-1
- 11-digit product format
- 696070008
- Labeler code
- 69607
- Product ID
- 69607-0008_b19ed0f4-2f3e-48c4-8029-3a6dc6908f17
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimonium Tartaricum, Arsenicum Album, Arsenicum Iodatum, Arum Triphyllum, Baptisia Tinctoria, Bryonia (Alba), Drosera (Rotundifolia), Echinacea Angustifolia, Eupatorium Perfoliatum, Kali Bromatum, Lung Suis, Mercurius Corrosivus, Sticta Pulmonaria, Sulphur Iodatum, Urtica Urens
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Biovea
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-02
- Marketing end
- 2022-03-18
- Substance
- ANTIMONY POTASSIUM TARTRATE; ARISAEMA TRIPHYLLUM ROOT; ARSENIC TRIIODIDE; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; DROSERA ROTUNDIFOLIA; ECHINACEA ANGUSTIFOLIA; EUPATORIUM PERFOLIATUM FLOWERING TOP; LOBARIA PULMONARIA; MERCURIC CHLORIDE; POTASSIUM BROMIDE; SULFUR IODIDE; SUS SCROFA LUNG; URTICA URENS
- Active strength
- 200 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/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
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record