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Discus Compositum Rx - 50114-4041-2 - (PSEUDOGNAPHALIUM OBTUSIFOLIUM and BERBERIS VULGARIS ROOT BARK and BLACK COHOSH and CINCHONA OFFICINALIS BARK and CITRULLUS COLOCYNTHIS FRUIT PULP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and HORSE CHESTNUT and ASCORBIC ACID and CUPRIC ACETATE and POTASSIUM CARBONATE and NADIDE and SODIUM DIETHYL OXALACETATE and NIACINAMIDE and TRINITROPHENOL and PULSATILLA VULGARIS and PYRIDOXINE HYDROCHLORIDE and RIBOFLAVIN and CLAVICEPS PURPUREA SCLEROTIUM and SILICON DIOXIDE)

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Drug Information of Discus Compositum Rx

Product NDC: 50114-4041
Proprietary Name: Discus Compositum Rx
Non Proprietary Name: PSEUDOGNAPHALIUM OBTUSIFOLIUM and BERBERIS VULGARIS ROOT BARK and BLACK COHOSH and CINCHONA OFFICINALIS BARK and CITRULLUS COLOCYNTHIS FRUIT PULP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and HORSE CHESTNUT and ASCORBIC ACID and CUPRIC ACETATE and POTASSIUM CARBONATE and NADIDE and SODIUM DIETHYL OXALACETATE and NIACINAMIDE and TRINITROPHENOL and PULSATILLA VULGARIS and PYRIDOXINE HYDROCHLORIDE and RIBOFLAVIN and CLAVICEPS PURPUREA SCLEROTIUM and SILICON DIOXIDE
Active Ingredient(s): 8; 8; 6; 4; 4; 4; 4; 6; 10; 6; 18; 6; 4; 10; 6; 6; 6; 3; 6; 6; 4; 6; 10; 6; 10; 6; 28; 10; 10; 8; 10; 8; 10; 6; 10; 6; 10    [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp;   PSEUDOGNAPHALIUM OBTUSIFOLIUM and BERBERIS VULGARIS ROOT BARK and BLACK COHOSH and CINCHONA OFFICINALIS BARK and CITRULLUS COLOCYNTHIS FRUIT PULP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and HORSE CHESTNUT and ASCORBIC ACID and CUPRIC ACETATE and POTASSIUM CARBONATE and NADIDE and SODIUM DIETHYL OXALACETATE and NIACINAMIDE and TRINITROPHENOL and PULSATILLA VULGARIS and PYRIDOXINE HYDROCHLORIDE and RIBOFLAVIN and CLAVICEPS PURPUREA SCLEROTIUM and SILICON DIOXIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Discus Compositum Rx

Product NDC: 50114-4041
Labeler Name: Heel Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20080830

Package Information of Discus Compositum Rx

Package NDC: 50114-4041-2
Package Description: 100 TABLET in 1 BOTTLE (50114-4041-2)

NDC Information of Discus Compositum Rx

NDC Code 50114-4041-2
Proprietary Name Discus Compositum Rx
Package Description 100 TABLET in 1 BOTTLE (50114-4041-2)
Product NDC 50114-4041
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PSEUDOGNAPHALIUM OBTUSIFOLIUM and BERBERIS VULGARIS ROOT BARK and BLACK COHOSH and CINCHONA OFFICINALIS BARK and CITRULLUS COLOCYNTHIS FRUIT PULP and LEDUM PALUSTRE TWIG and RANUNCULUS BULBOSUS and HORSE CHESTNUT and ASCORBIC ACID and CUPRIC ACETATE and POTASSIUM CARBONATE and NADIDE and SODIUM DIETHYL OXALACETATE and NIACINAMIDE and TRINITROPHENOL and PULSATILLA VULGARIS and PYRIDOXINE HYDROCHLORIDE and RIBOFLAVIN and CLAVICEPS PURPUREA SCLEROTIUM and SILICON DIOXIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080830
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; ASCORBIC ACID; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CLAVICEPS PURPUREA SCLEROTIUM; COENZYME A; CUPRIC ACETATE; GONORRHEAL URETHRAL SECRETION HUMAN; HORSE CHESTNUT; LEDUM PALUSTRE TWIG; MERCURIC OXIDE, YELLOW; NADIDE; NIACINAMIDE; POTASSIUM CARBONATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM; PULSATILLA VULGARIS; PYRIDOXINE HYDROCHLORIDE; RANUNCULUS BULBOSUS; RIBOFLAVIN; SEPIA OFFICINALIS JUICE; SILICO
Strength Number 8; 8; 6; 4; 4; 4; 4; 6; 10; 6; 18; 6; 4; 10; 6; 6; 6; 3; 6; 6; 4; 6; 10; 6; 10; 6; 28; 10; 10; 8; 10; 8; 10; 6; 10; 6; 10
Strength Unit [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmaceutical Classes Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

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