Ver
- Product NDC
- 43742-0167
- 11-digit product format
- 437420167
- Labeler code
- 43742
- Product ID
- 43742-0167_638d228f-3ff1-4001-8496-54da67329bc0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Artemisia vulgaris, Filix mas, Cina, Melilotus officinalis, Quassia amara, Spigelia anthelmia, Teucrium marum, Thymus serpyllum, Siliceea, Calcarea carbonica,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-11-14
- Marketing end
- 2019-10-13
- Substance
- ARTEMISIA VULGARIS ROOT; DRYOPTERIS FILIX-MAS ROOT; ARTEMISIA CINA PRE-FLOWERING TOP; MELILOTUS OFFICINALIS TOP; QUASSIA AMARA WOOD; SPIGELIA ANTHELMIA; TEUCRIUM MARUM; THYMUS SERPYLLUM; SILICON DIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GRAPHITE; IODINE; MERCURIC CHLORIDE; SCHOENOCAULON OFFICINALE SEED; ASCARIS LUMBRICOIDES; TRICHINELLA SPIRALIS; ENTEROBIUS VERMICULARIS; TAENIA SOLIUM; TRICHOMONAS VAGINALIS; GIARDIA LAMBLIA; CRYPTOSPORIDIUM PARVUM; TAENIA SAGINATA; BRUGIA MALAYI
- Active strength
- 2 [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; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record