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Arthritis Joints - 57520-0925-1 - (Gnaphalium polycephalum, Berberis vulgaris, Cimicifuga racemosa, Cinchona officinalis, Colocynthis, Ledum palustre, Ranunculus bulbosus, Aesculus hippocastanum, Borax, Cuprum aceticum, Kali carbonicum)

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Drug Information of Arthritis Joints

Product NDC: 57520-0925
Proprietary Name: Arthritis Joints
Non Proprietary Name: Gnaphalium polycephalum, Berberis vulgaris, Cimicifuga racemosa, Cinchona officinalis, Colocynthis, Ledum palustre, Ranunculus bulbosus, Aesculus hippocastanum, Borax, Cuprum aceticum, Kali carbonicum
Active Ingredient(s): 8; 4; 4; 4; 4; 6; 6; 6; 4; 10; 12; 6; 3; 6; 4; 10; 8; 10; 6; 30; 10; 12; 12; 12; 10; 12; 10    [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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Gnaphalium polycephalum, Berberis vulgaris, Cimicifuga racemosa, Cinchona officinalis, Colocynthis, Ledum palustre, Ranunculus bulbosus, Aesculus hippocastanum, Borax, Cuprum aceticum, Kali carbonicum
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Arthritis Joints

Product NDC: 57520-0925
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20111024

Package Information of Arthritis Joints

Package NDC: 57520-0925-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0925-1)

NDC Information of Arthritis Joints

NDC Code 57520-0925-1
Proprietary Name Arthritis Joints
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0925-1)
Product NDC 57520-0925
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Gnaphalium polycephalum, Berberis vulgaris, Cimicifuga racemosa, Cinchona officinalis, Colocynthis, Ledum palustre, Ranunculus bulbosus, Aesculus hippocastanum, Borax, Cuprum aceticum, Kali carbonicum
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20111024
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name AMMONIUM CHLORIDE; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CLAVICEPS PURPUREA SCLEROTIUM; CUPRIC ACETATE; HORSE CHESTNUT; LEDUM PALUSTRE TWIG; MERCURIC OXIDE, YELLOW; PALLADIUM; POTASSIUM CARBONATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM; PULSATILLA VULGARIS; RANUNCULUS BULBOSUS; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SILVER; SODIUM BORATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA CARTILAGE; SUS SCROFA INTERVER
Strength Number 8; 4; 4; 4; 4; 6; 6; 6; 4; 10; 12; 6; 3; 6; 4; 10; 8; 10; 6; 30; 10; 12; 12; 12; 10; 12; 10
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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Arthritis Joints


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