| 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 |