- Product NDC
- 58066-7002
- 11-digit product format
- 580667002
- Labeler code
- 58066
- Product ID
- 58066-7002_7a6df16b-e570-419a-9b7c-0d87c0c0c5a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Agaricus muscarius, Alumina, Anagallis arvensis, Antimonium tartaricum, Apis mellifica, Arsenicum album, Arsenicum iodatum, Bovista, Causticum, Dolichos pruriens, Fagapyrum esculentum, Graphites, Kali muriaticum, Lac defloratum, Muriaticum acidum, Oleander, Petroleum, Pix Liquida, Radium bromatum, Rhus toxicodendron, Selenium metallicum, Sulphur, Urtica urens
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Beaumont Bio Med
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-01-16
- Marketing end
- 0000-00-00
- Substance
- AMANITA MUSCARIA FRUITING BODY; ALUMINUM OXIDE; ANAGALLIS ARVENSIS; ANTIMONY POTASSIUM TARTRATE; APIS MELLIFERA; ARSENIC TRIOXIDE; ARSENIC TRIIODIDE; LYCOPERDON UTRIFORME FRUITING BODY; CAUSTICUM; MUCUNA PRURIENS FRUIT TRICHOME; FAGOPYRUM ESCULENTUM; GRAPHITE; POTASSIUM CHLORIDE; SKIM MILK; HYDROCHLORIC ACID; NERIUM OLEANDER LEAF; KEROSENE; PINE TAR; RADIUM BROMIDE; TOXICODENDRON PUBESCENS LEAF; SELENIUM; SULFUR; URTICA URENS
- Active strength
- 10 [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL; [hp_X]/59.2mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record