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Aconitum Homaccord
Aconitum Homaccord - 50114-1180-4 - (ACONITUM NAPELLUS and EUCALYPTUS GLOBULUS LEAF and IPECAC)
Drug Information of Aconitum Homaccord
| Product NDC: | 50114-1180 |
| Proprietary Name: | Aconitum Homaccord |
| Non Proprietary Name: | ACONITUM NAPELLUS and EUCALYPTUS GLOBULUS LEAF and IPECAC |
| Active Ingredient(s): | 3; 2; 3 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL & nbsp; ACONITUM NAPELLUS and EUCALYPTUS GLOBULUS LEAF and IPECAC |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aconitum Homaccord
| Product NDC: | 50114-1180 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19860131 |
Package Information of Aconitum Homaccord
| Package NDC: | 50114-1180-4 |
| Package Description: | 50 mL in 1 BOTTLE (50114-1180-4) |
NDC Information of Aconitum Homaccord
| NDC Code | 50114-1180-4 |
| Proprietary Name | Aconitum Homaccord |
| Package Description | 50 mL in 1 BOTTLE (50114-1180-4) |
| Product NDC | 50114-1180 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACONITUM NAPELLUS and EUCALYPTUS GLOBULUS LEAF and IPECAC |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19860131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ACONITUM NAPELLUS; EUCALYPTUS GLOBULUS LEAF; IPECAC |
| Strength Number | 3; 2; 3 |
| Strength Unit | [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL |
| Pharmaceutical Classes |
