Envirotox - 43857-0040-1 - (Triticum Aestivum, Berberis Vulgaris, Lappa Major, Phytolacca Decandra, Rhamnus Cathartica, Rhamnus Purshiana,)

Alphabetical Index


Drug Information of Envirotox

Product NDC: 43857-0040
Proprietary Name: Envirotox
Non Proprietary Name: Triticum Aestivum, Berberis Vulgaris, Lappa Major, Phytolacca Decandra, Rhamnus Cathartica, Rhamnus Purshiana,
Active Ingredient(s): 9; 9; 3; 12; 3; 3; 6; 12; 12; 12; 3; 9; 3; 9; 9; 9; 6; 12; 6; 1; 9; 6    [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;   Triticum Aestivum, Berberis Vulgaris, Lappa Major, Phytolacca Decandra, Rhamnus Cathartica, Rhamnus Purshiana,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Envirotox

Product NDC: 43857-0040
Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130123

Package Information of Envirotox

Package NDC: 43857-0040-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43857-0040-1)

NDC Information of Envirotox

NDC Code 43857-0040-1
Proprietary Name Envirotox
Package Description 30 mL in 1 BOTTLE, DROPPER (43857-0040-1)
Product NDC 43857-0040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Triticum Aestivum, Berberis Vulgaris, Lappa Major, Phytolacca Decandra, Rhamnus Cathartica, Rhamnus Purshiana,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130123
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name BioActive Nutritional, Inc.
Substance Name ACETONE; AMMONIUM CHLORIDE; ARCTIUM LAPPA ROOT; ATROPA BELLADONNA WHOLE; BERBERIS VULGARIS ROOT BARK; FRANGULA PURSHIANA BARK; GLYCYRRHIZA GLABRA; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; PROPYLENE GLYCOL; RHAMNUS CATHARTICA FRUIT; SODIUM BENZENESULFONATE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE; STILLINGIA SYLVATICA ROOT; STRYCHNOS NUX-VOMICA SEED; TRIFOLIUM PRATENSE FLOWER; TRITICUM AESTIVUM WHOLE; TURPENTINE OIL; ZANTHOXYLUM AMERICANUM BARK</t
Strength Number 9; 9; 3; 12; 3; 3; 6; 12; 12; 12; 3; 9; 3; 9; 9; 9; 6; 12; 6; 1; 9; 6
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
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Seed Storage Proteins [Chemical/Ingredient]

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