ALL FLU
- Product NDC
- 50181-0044
- 11-digit product format
- 501810044
- Labeler code
- 50181
- Product ID
- 50181-0044_dc661061-8839-44b0-a568-c05e52cc7893
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus, Arsenicum iodatum, Bryonia (Alba), Eupatorium perfoliatum, Gelsenium sempervirens, Helix tosta,
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- The Wellness Center For Research and Education
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-06-19
- Marketing end
- 2019-07-14
- Substance
- ACONITUM NAPELLUS; ARSENIC TRIIODIDE; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; ESCARGOT SHELL, COOKED; HYDROGEN; INFLUENZA A VIRUS A/CALIFORNIA/7/2009 X-179A (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/PERTH/16/2009 (H3N2) LIVE (ATTENUATED) ANTIGEN; INFLUENZA B VIRUS B/BRISBANE/60/2008 ANTIGEN (FORMALDEHYDE INACTIVATED); WOOD CREOSOTE; PHOSPHORUS; TEUCRIUM SCORODONIA FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; VERATRUM VIRIDE ROOT; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
- Active strength
- 30 [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g; [hp_C]/g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record