- Product NDC
- 50845-0135
- 11-digit product format
- 508450135
- Labeler code
- 50845
- Product ID
- 50845-0135_dc7663f0-b12e-43ef-8c0c-e0453768a584
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anthracinum, Apis Mellifica, Arnica Montana, Calendula Officinalis, Conium Maculatum, Echinacea (Angustifolia), Euphorbia Pilulifera, Grindelia, Histaminum Hydrochloricum, Hypericum perforatum, Lachesis Mutus, Latrodectus Mactans, Ledum Palustre, Pyrogenium, Tarentula Cubensis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Liddell Laboratories, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-07-07
- Marketing end
- 2025-11-10
- Substance
- BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; APIS MELLIFERA; ARNICA MONTANA; CALENDULA OFFICINALIS FLOWERING TOP; CONIUM MACULATUM FLOWERING TOP; ECHINACEA ANGUSTIFOLIA; EUPHORBIA HIRTA FLOWERING TOP; GRINDELIA HIRSUTULA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; HYPERICUM PERFORATUM; LACHESIS MUTA VENOM; LATRODECTUS MACTANS; LEDUM PALUSTRE TWIG; RANCID BEEF; CITHARACANTHUS SPINICRUS
- Active strength
- 200 [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record