- Product NDC
- 50181-0054
- 11-digit product format
- 501810054
- Labeler code
- 50181
- Product ID
- 50181-0054_bb63efa1-2908-4b4d-b9b6-1394dafae306
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Arsenicum Iodatum, Bryonia (Alba), Eupatorium Perfoliatum, Gelsemium Sempervirens, Helix Tosta, Hydrogen, Influenzinum, Kreosotum, Phosphorus, Teucrium Scorodonia, Thuja Occidentalis, Veratrum Viride, Anas Barbariae, Hepatis Et Cordis Extractum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- The Wellness Center For Research and Education
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-03-12
- Marketing end
- 0000-00-00
- Substance
- ACONITUM NAPELLUS; ARSENIC TRIIODIDE; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; ESCARGOT SHELL, COOKED; HYDROGEN; INFLUENZA A VIRUS; INFLUENZA B VIRUS; WOOD CREOSOTE; PHOSPHORUS; TEUCRIUM SCORODONIA FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; VERATRUM VIRIDE ROOT; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
- Active strength
- 30 [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record