"50845-0200-1" National Drug Code (NDC)

Candida Yeast 30 mL in 1 BOTTLE, SPRAY (50845-0200-1)
(Liddell Laboratories, Inc.)

NDC Code50845-0200-1
Package Description30 mL in 1 BOTTLE, SPRAY (50845-0200-1)
Product NDC50845-0200
Product Type NameHUMAN OTC DRUG
Proprietary NameCandida Yeast
Non-Proprietary NameBaptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Echinacea (angustifolia), Kreosotum, Mercurius Cyanatus, Mercurius Sulphuratus Ruber, Nitricum Acidum, Pyrogenium, Sulphuricum Acidum, Thuja Occidentalis
Dosage FormSPRAY
UsageORAL
Start Marketing Date20140221
End Marketing Date20230129
Marketing Category NameUNAPPROVED HOMEOPATHIC
ManufacturerLiddell Laboratories, Inc.
Substance NameBAPTISIA TINCTORIA; CANDIDA ALBICANS; CANDIDA PARAPSILOSIS; ECHINACEA ANGUSTIFOLIA; MERCURIC CYANIDE; MERCURIC SULFIDE; NITRIC ACID; RANCID BEEF; SODIUM BORATE; SULFURIC ACID; THUJA OCCIDENTALIS LEAF; WOOD CREOSOTE
Strength3; 12; 8; 3; 30; 30; 30; 200; 30; 30; 30; 30
Strength Unit[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]

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