- Product NDC
- 43772-0052
- 11-digit product format
- 437720052
- Labeler code
- 43772
- Product ID
- 43772-0052_cda54fe6-29c5-4a32-ab05-2942384c5988
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Baptisia Tinctoria, Chelidonium Majus, Hydrastis Canadensis, Phytolacca Decandra, Tabebuia Impetiginosa, Taraxacum Officinale, Uncaria Tomentosa, Thuja Occidentalis, Calcarea Carbonica, Silicea, Belladonna, Chamomilla, Lycopodium Clavatum, Rhus Tox, Arsenicum Album, Pertussinum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Synergy Formulas, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-03-19
- Marketing end
- 0000-00-00
- Substance
- ECHINACEA ANGUSTIFOLIA; BAPTISIA TINCTORIA ROOT; CHELIDONIUM MAJUS; GOLDENSEAL; PHYTOLACCA AMERICANA ROOT; TABEBUIA IMPETIGINOSA BARK; TARAXACUM OFFICINALE; CAT'S CLAW; THUJA OCCIDENTALIS LEAFY TWIG; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; ATROPA BELLADONNA; MATRICARIA RECUTITA; LYCOPODIUM CLAVATUM SPORE; TOXICODENDRON PUBESCENS LEAF; ARSENIC TRIOXIDE; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
- Active strength
- 1 [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