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