- Product NDC
- 43772-0047
- 11-digit product format
- 437720047
- Labeler code
- 43772
- Product ID
- 43772-0047_980ee156-06d4-4959-a121-3620d5c35c56
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triticum Aestivum, Cajuputum, Baptisia Tinctoria, Capsicum Annuum, Frasera Caroliniensis, Quassia (Amara), Senna (Cassia Angustifolia), Absinthium, Hepar Bovine, Spleen (Bovine), Glandula Suprarenalis Bovine, Cinchona Officinalis, Lycopodium Clavatum, Amoeba Axis, Giardia Lamblia
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Synergy Formulas, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-21
- Marketing end
- 0000-00-00
- Substance
- TRITICUM AESTIVUM WHOLE; CAJUPUT OIL; BAPTISIA TINCTORIA; CAPSICUM; FRASERA CAROLINIENSIS ROOT; QUASSIA AMARA WOOD; SENNA LEAF; WORMWOOD; BEEF LIVER; BOS TAURUS SPLEEN; BOS TAURUS ADRENAL GLAND; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; AMOEBA PROTEUS; GIARDIA LAMBLIA
- 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_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record