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Fungal Infection - 55714-4618-2 - (Candida albicans, Sanicula, Tellurium metallicum, Torula cerevisiae, Antimon. crud., Arsenicum alb., Baryta carb., Bryonia, Calc. carb., Carbo veg., Cuprum met., Dulcamara, Graphites, Kali carb., Lachesis, Lycopodium, Mezereum, Nitricum ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum ac., Zinc. met., Apis mel., Phytolacca, Thuja.)

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Drug Information of Fungal Infection

Product NDC: 55714-4618
Proprietary Name: Fungal Infection
Non Proprietary Name: Candida albicans, Sanicula, Tellurium metallicum, Torula cerevisiae, Antimon. crud., Arsenicum alb., Baryta carb., Bryonia, Calc. carb., Carbo veg., Cuprum met., Dulcamara, Graphites, Kali carb., Lachesis, Lycopodium, Mezereum, Nitricum ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum ac., Zinc. met., Apis mel., Phytolacca, Thuja.
Active Ingredient(s): 15; 15; 3; 8; 15; 15; 15; 20; 15; 15; 15; 15; 15; 15; 15; 15; 15; 3; 8; 15; 20; 20; 15; 15; 15; 15; 15; 20; 3; 8; 15    [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; [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; [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; [hp_X]/mL & nbsp;   Candida albicans, Sanicula, Tellurium metallicum, Torula cerevisiae, Antimon. crud., Arsenicum alb., Baryta carb., Bryonia, Calc. carb., Carbo veg., Cuprum met., Dulcamara, Graphites, Kali carb., Lachesis, Lycopodium, Mezereum, Nitricum ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum ac., Zinc. met., Apis mel., Phytolacca, Thuja.
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Fungal Infection

Product NDC: 55714-4618
Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110601

Package Information of Fungal Infection

Package NDC: 55714-4618-2
Package Description: 59.14 mL in 1 BOTTLE, GLASS (55714-4618-2)

NDC Information of Fungal Infection

NDC Code 55714-4618-2
Proprietary Name Fungal Infection
Package Description 59.14 mL in 1 BOTTLE, GLASS (55714-4618-2)
Product NDC 55714-4618
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Candida albicans, Sanicula, Tellurium metallicum, Torula cerevisiae, Antimon. crud., Arsenicum alb., Baryta carb., Bryonia, Calc. carb., Carbo veg., Cuprum met., Dulcamara, Graphites, Kali carb., Lachesis, Lycopodium, Mezereum, Nitricum ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum ac., Zinc. met., Apis mel., Phytolacca, Thuja.
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Newton Laboratories, Inc.
Substance Name ACTIVATED CHARCOAL; ANTIMONY TRISULFIDE; APIS MELLIFERA; APIS MELLIFERA; ARSENIC TRIOXIDE; BARIUM CARBONATE; BRYONIA ALBA ROOT; CANDIDA ALBICANS; COPPER; DAPHNE MEZEREUM BARK; GRAPHITE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PHYTOLACCA AMERICANA ROOT; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; SACCHAROMYCES CEREVISIAE; SANICULA EUROPAEA LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SOLANUM
Strength Number 15; 15; 3; 8; 15; 15; 15; 20; 15; 15; 15; 15; 15; 15; 15; 15; 15; 3; 8; 15; 20; 20; 15; 15; 15; 15; 15; 20; 3; 8; 15
Strength Unit [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; [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; [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; [hp_X]/mL
Pharmaceutical Classes Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Fungal Proteins [Chemical/Ingredient],Non-Standardized Fungal Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Dietary Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient],Fungal Proteins [Chemical/Ingredient],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE],Standardized Insect Venom Protein Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Bee Venoms [Chemical/Ingredient],Standardized Insect Venom Protein Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Bee Venoms [Chemical/Ingredient]

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