Home > National Drug Code (NDC) > Nux Vomica Homaccord

Nux Vomica Homaccord - 50114-5285-6 - (CITRULLUS COLOCYNTHIS FRUIT PULP and LYCOPODIUM CLAVATUM SPORE and BRYONIA ALBA ROOT and STRYCHNOS NUX-VOMICA SEED)

Alphabetical Index


Drug Information of Nux Vomica Homaccord

Product NDC: 50114-5285
Proprietary Name: Nux Vomica Homaccord
Non Proprietary Name: CITRULLUS COLOCYNTHIS FRUIT PULP and LYCOPODIUM CLAVATUM SPORE and BRYONIA ALBA ROOT and STRYCHNOS NUX-VOMICA SEED
Active Ingredient(s): 4; 5; 5; 4    [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL & nbsp;   CITRULLUS COLOCYNTHIS FRUIT PULP and LYCOPODIUM CLAVATUM SPORE and BRYONIA ALBA ROOT and STRYCHNOS NUX-VOMICA SEED
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nux Vomica Homaccord

Product NDC: 50114-5285
Labeler Name: Heel Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19930131

Package Information of Nux Vomica Homaccord

Package NDC: 50114-5285-6
Package Description: 10 VIAL in 1 CARTON (50114-5285-6) > 1.1 mL in 1 VIAL

NDC Information of Nux Vomica Homaccord

NDC Code 50114-5285-6
Proprietary Name Nux Vomica Homaccord
Package Description 10 VIAL in 1 CARTON (50114-5285-6) > 1.1 mL in 1 VIAL
Product NDC 50114-5285
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CITRULLUS COLOCYNTHIS FRUIT PULP and LYCOPODIUM CLAVATUM SPORE and BRYONIA ALBA ROOT and STRYCHNOS NUX-VOMICA SEED
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19930131
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED
Strength Number 4; 5; 5; 4
Strength Unit [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL
Pharmaceutical Classes

Complete Information of Nux Vomica Homaccord


General Information