- Product NDC
- 44911-0119
- 11-digit product format
- 449110119
- Labeler code
- 44911
- Product ID
- 44911-0119_cda34e50-0e47-471a-a677-76fd4cc718ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Tabebuia impetiginosa, Abies nigra, Lycopodium clavatum, Nux vomica, Phosphorus, Pulsatilla (Vulgaris), Sepia, Skatolum, Canadida albicans,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-05-05
- Marketing end
- 2025-07-15
- Substance
- CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; PICEA MARIANA RESIN; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; SKATOLE; STRYCHNOS NUX-VOMICA SEED; TABEBUIA IMPETIGINOSA BARK
- Active strength
- 30 [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
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record