- Product NDC
- 43742-0674
- 11-digit product format
- 437420674
- Labeler code
- 43742
- Product ID
- 43742-0674_1610641b-29ac-4739-b037-b4986aa67272
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Condurango, Echinacea (Angustifolia), Ginkgo Biloba, Hydrastis Canadensis, Ligusticum Porteri, Myrrha, Phytolacca Decandra, Tabebuia Impetiginosa, Propolis, Glandula Suprarenalis Suis, Spleen (Suis), Thymus (Suis), Thyroidinum (Suis), Gelsemium Sempervirens, Lycopodium Clavatum, Nux Vomica, Selenium Metallicum, Pyrogenium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-11-24
- Marketing end
- 2020-12-13
- Substance
- MARSDENIA CONDURANGO BARK; ECHINACEA ANGUSTIFOLIA; GINKGO; GOLDENSEAL; LIGUSTICUM PORTERI ROOT; MYRRH; PHYTOLACCA AMERICANA ROOT; TABEBUIA IMPETIGINOSA BARK; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; THYROID, PORCINE; GELSEMIUM SEMPERVIRENS ROOT; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; SELENIUM; RANCID BEEF
- 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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record