- Product NDC
- 57955-0076
- 11-digit product format
- 579550076
- Labeler code
- 57955
- Product ID
- 57955-0076_99db1291-1eaf-4ab9-a191-e86706b4bd97
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Abies nigra, Antimonium crudum, Asafoetida, Baptisia tinctoria, Borax, Candida albicans, Lachesis mutus, Phosphoricum acidum, Phytolacca decandra, Pulsatilla, Sticta Plumonaria, Sulphur, Thuja occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-02-26
- Marketing end
- 0000-00-00
- Substance
- PICEA MARIANA RESIN; ANTIMONY TRISULFIDE; ASAFETIDA; BAPTISIA TINCTORIA ROOT; SODIUM BORATE; CANDIDA ALBICANS; LACHESIS MUTA VENOM; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; LOBARIA PULMONARIA; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- Pharmacologic classes
- Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record