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Colocynthis-Homaccord - 50114-1034-6 - (CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM)

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Drug Information of Colocynthis-Homaccord

Product NDC: 50114-1034
Proprietary Name: Colocynthis-Homaccord
Non Proprietary Name: CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM
Active Ingredient(s): 4; 3    [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp;   CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Colocynthis-Homaccord

Product NDC: 50114-1034
Labeler Name: Heel Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19930131

Package Information of Colocynthis-Homaccord

Package NDC: 50114-1034-6
Package Description: 10 VIAL in 1 CARTON (50114-1034-6) > 1.1 mL in 1 VIAL

NDC Information of Colocynthis-Homaccord

NDC Code 50114-1034-6
Proprietary Name Colocynthis-Homaccord
Package Description 10 VIAL in 1 CARTON (50114-1034-6) > 1.1 mL in 1 VIAL
Product NDC 50114-1034
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19930131
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM
Strength Number 4; 3
Strength Unit [hp_X]/1.1mL; [hp_X]/1.1mL
Pharmaceutical Classes

Complete Information of Colocynthis-Homaccord


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