| Product NDC: | 0220-3681 |
| Proprietary Name: | Nux Vomica |
| Non Proprietary Name: | STRYCHNOS NUX-VOMICA SEED |
| Active Ingredient(s): | 30 [hp_C]/1 & nbsp; STRYCHNOS NUX-VOMICA SEED |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0220-3681 |
| Labeler Name: | Laboratoires Boiron |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120101 |
| Package NDC: | 0220-3681-43 |
| Package Description: | 3 TUBE in 1 PACKAGE (0220-3681-43) > 80 PELLET in 1 TUBE (0220-3681-41) |
| NDC Code | 0220-3681-43 |
| Proprietary Name | Nux Vomica |
| Package Description | 3 TUBE in 1 PACKAGE (0220-3681-43) > 80 PELLET in 1 TUBE (0220-3681-41) |
| Product NDC | 0220-3681 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | STRYCHNOS NUX-VOMICA SEED |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Laboratoires Boiron |
| Substance Name | STRYCHNOS NUX-VOMICA SEED |
| Strength Number | 30 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |