Matrix Support

Product NDC
43742-0030
11-digit product format
437420030
Labeler code
43742
Product ID
43742-0030_2dac9db6-13af-474f-9eed-6d141141cda6
Type
HUMAN OTC DRUG
Nonproprietary name
Ceanothus Americanus, Hydrastis Canadensis, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Momordica Balsamina, Oxalis Acetosella, Pulsatilla, Bile Duct (Suis), Colon (Suis), Duodenum (Suis), Esophagus (Suis), Eye (Suis), Gallbladder (Suis), Ileum (Suis), Intestine (Suis), Ipecacuanha, Jejunum (Suis), Kali Bichromicum, Lung (Suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (Suis), Pancreas Suis, Phosphorus, Rectum (Suis), Stomach (Suis), Sulphur, Mannan
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2012-05-14
Marketing end
2020-09-15
Substance
CEANOTHUS AMERICANUS LEAF; GOLDENSEAL; VERATRUM ALBUM ROOT; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; MARSDENIA CONDURANGO BARK; MOMORDICA BALSAMINA IMMATURE FRUIT; OXALIS ACETOSELLA LEAF; PULSATILLA VULGARIS; SUS SCROFA BILE DUCT; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA EYE; SUS SCROFA GALLBLADDER; SUS SCROFA ILEUM; PORK INTESTINE; IPECAC; SUS SCROFA JEJUNUM; POTASSIUM DICHROMATE; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; SODIUM DIETHYL OXALACETATE; SUS SCROFA ORAL MUCOSA; SUS SCROFA PANCREAS; PHOSPHORUS; SUS SCROFA RECTUM; SUS SCROFA STOMACH; SULFUR; YEAST MANNAN; ATROPA BELLADONNA; WOOD CREOSOTE; LACHESIS MUTA VENOM; MANDRAGORA OFFICINARUM ROOT; SUS SCROFA URINARY BLADDER; SHIGELLA DYSENTERIAE
Active strength
4 [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_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_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
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record