- Product NDC
- 50181-0035
- 11-digit product format
- 501810035
- Labeler code
- 50181
- Product ID
- 50181-0035_6803ba40-83b1-4ef4-a574-155d7e256db8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cochlearia Armoracia, Phytolacca Decandra, Chelidonium Majus, Intestinal Mucosa, Spleen, Hepar Bovine, Thymus, Salmonella Enteritidis, Helicobacter Pylori, Nux Vomica, Salmonella Paratyphi, Botulinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-01-03
- Marketing end
- 0000-00-00
- Substance
- HORSERADISH; PHYTOLACCA AMERICANA ROOT; CHELIDONIUM MAJUS; BOS TAURUS INTESTINAL MUCOSA; SUS SCROFA SPLEEN; BEEF LIVER; SUS SCROFA THYMUS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; HELICOBACTER PYLORI; STRYCHNOS NUX-VOMICA SEED; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI; BOTULINUM TOXIN TYPE A
- 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_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record