| Product NDC: | 48951-7063 |
| Proprietary Name: | Myristica Argentum Sinus Relief |
| Non Proprietary Name: | POTASSIUM DICHROMATE SUS SCROFA NASAL MUCOSA SILVER NITRATE |
| Active Ingredient(s): | 6; 20; 7 [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; POTASSIUM DICHROMATE SUS SCROFA NASAL MUCOSA SILVER NITRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 48951-7063 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090901 |
| Package NDC: | 48951-7063-2 |
| Package Description: | 1350 PELLET in 1 BOTTLE, GLASS (48951-7063-2) |
| NDC Code | 48951-7063-2 |
| Proprietary Name | Myristica Argentum Sinus Relief |
| Package Description | 1350 PELLET in 1 BOTTLE, GLASS (48951-7063-2) |
| Product NDC | 48951-7063 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | POTASSIUM DICHROMATE SUS SCROFA NASAL MUCOSA SILVER NITRATE |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | POTASSIUM DICHROMATE; SILVER NITRATE; SUS SCROFA NASAL MUCOSA |
| Strength Number | 6; 20; 7 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |