Sinuforce
- Product NDC
- 43857-0290
- 11-digit product format
- 438570290
- Labeler code
- 43857
- Product ID
- 43857-0290_71f51df0-faf9-414b-8d94-dae5af172d37
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Hydrastis Canadensis, Nux Moschata, Trigonella Foenum Graecum, Arsenicum Album, Kali Bichromicum, Mercurius Sulphuratus Ruber, Pulsatilla (Vulgaris), Sepia, Mercurius Solubilis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-03-21
- Marketing end
- 2020-11-18
- Substance
- ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; NUTMEG; FENUGREEK SEED; ARSENIC TRIOXIDE; POTASSIUM DICHROMATE; MERCURIC SULFIDE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; MERCURIUS SOLUBILIS
- 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
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record