- Product NDC
- 50181-0043
- 11-digit product format
- 501810043
- Labeler code
- 50181
- Product ID
- 50181-0043_05b13696-c2ab-4590-b884-dd2341617548
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chelidonium Majus, Fucus Vesiculosus, Hypericum Perforatum, Sulphur, Cesium Chloride, Glandula Suprarenalis Suis, Thyroidinum (Suis), Strontium Carbonicum, Cadmium Iodatum, Cadmium Sulphuricum, X-Ray, Radium Bromatum, Uranium Nitricum, Electricitas, Plutonium Nitricum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-05-13
- Marketing end
- 0000-00-00
- Substance
- CHELIDONIUM MAJUS; FUCUS VESICULOSUS; HYPERICUM PERFORATUM; SULFUR; CESIUM CHLORIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYROID; STRONTIUM CARBONATE; CADMIUM IODIDE; CADMIUM SULFATE; ALCOHOL, X-RAY EXPOSED (1000 RAD); RADIUM BROMIDE; URANYL NITRATE HEXAHYDRATE; LACTOSE; PLUTONIUM
- Active strength
- 3 [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; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record