Arthritis - 50114-4290-2 - (BRYONIA ALBA ROOT and TOXICODENDRON PUBESCENS LEAF and CITRULLUS COLOCYNTHIS FRUIT PULP and ARNICA MONTANA ROOT and COLCHICUM AUTUMNALE BULB and SOLANUM DULCAMARA TOP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and BERBERIS VULGARIS ROOT BARK and CAUSTICUM and RHODODENDRON AUREUM LEAF and LYCOPODIUM CLAVATUM SPORE and SULFUR and FERROSOFERRIC PHOSPHATE)

Alphabetical Index


Drug Information of Arthritis

Product NDC: 50114-4290
Proprietary Name: Arthritis
Non Proprietary Name: BRYONIA ALBA ROOT and TOXICODENDRON PUBESCENS LEAF and CITRULLUS COLOCYNTHIS FRUIT PULP and ARNICA MONTANA ROOT and COLCHICUM AUTUMNALE BULB and SOLANUM DULCAMARA TOP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and BERBERIS VULGARIS ROOT BARK and CAUSTICUM and RHODODENDRON AUREUM LEAF and LYCOPODIUM CLAVATUM SPORE and SULFUR and FERROSOFERRIC PHOSPHATE
Active Ingredient(s): 6; 8; 4; 8; 5; 6; 12; 6; 10; 6; 8; 6; 10; 4    [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp;   BRYONIA ALBA ROOT and TOXICODENDRON PUBESCENS LEAF and CITRULLUS COLOCYNTHIS FRUIT PULP and ARNICA MONTANA ROOT and COLCHICUM AUTUMNALE BULB and SOLANUM DULCAMARA TOP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and BERBERIS VULGARIS ROOT BARK and CAUSTICUM and RHODODENDRON AUREUM LEAF and LYCOPODIUM CLAVATUM SPORE and SULFUR and FERROSOFERRIC PHOSPHATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Arthritis

Product NDC: 50114-4290
Labeler Name: Heel Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20000930

Package Information of Arthritis

Package NDC: 50114-4290-2
Package Description: 30000 mg in 1 BOTTLE (50114-4290-2)

NDC Information of Arthritis

NDC Code 50114-4290-2
Proprietary Name Arthritis
Package Description 30000 mg in 1 BOTTLE (50114-4290-2)
Product NDC 50114-4290
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BRYONIA ALBA ROOT and TOXICODENDRON PUBESCENS LEAF and CITRULLUS COLOCYNTHIS FRUIT PULP and ARNICA MONTANA ROOT and COLCHICUM AUTUMNALE BULB and SOLANUM DULCAMARA TOP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and BERBERIS VULGARIS ROOT BARK and CAUSTICUM and RHODODENDRON AUREUM LEAF and LYCOPODIUM CLAVATUM SPORE and SULFUR and FERROSOFERRIC PHOSPHATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000930
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name ARNICA MONTANA ROOT; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; CAUSTICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; COLCHICUM AUTUMNALE BULB; FERROSOFERRIC PHOSPHATE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; RANUNCULUS BULBOSUS; RHODODENDRON AUREUM LEAF; SOLANUM DULCAMARA TOP; SULFUR; TOXICODENDRON PUBESCENS LEAF
Strength Number 6; 8; 4; 8; 5; 6; 12; 6; 10; 6; 8; 6; 10; 4
Strength Unit [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg
Pharmaceutical Classes

Complete Information of Arthritis


General Information