- Product NDC
- 43772-0021
- 11-digit product format
- 437720021
- Labeler code
- 43772
- Product ID
- 43772-0021_8a825f9d-8892-45bb-b404-8537ccb0bbae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chelidonium majus, Echinacea (Angustifolia), Hydrastis canadensis, Nasturtium aquaticum, Taraxacum officinale, Trifolium pratense, Rhus toxicodendron, Arnica montana,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Synergy Formulas, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-06-23
- Marketing end
- 0000-00-00
- Substance
- CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; NASTURTIUM AQUATICUM; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER; TOXICODENDRON PUBESCENS LEAF; ARNICA MONTANA; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA THYMUS; OXALIC ACID; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; LATRODECTUS MACTANS; BORRELIA BURGDORFERI; JAPANESE ENCEPHALITIS VIRUS; NEISSERIA MENINGITIDIS; HEPATITIS B VIRUS
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record