Product NDC: | 48951-3037 |
Proprietary Name: | Cartilago Argentum Joint Support |
Non Proprietary Name: | MANDRAGORA OFFICINARUM ROOT BETULA PENDULA LEAF ACONITUM NAPELLUS ROOT ARNICA MONTANA SILVER |
Active Ingredient(s): | 6; 6; 5; 5; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; MANDRAGORA OFFICINARUM ROOT BETULA PENDULA LEAF ACONITUM NAPELLUS ROOT ARNICA MONTANA SILVER |
Administration Route(s): | ORAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48951-3037 |
Labeler Name: | Uriel Pharmacy Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090901 |
Package NDC: | 48951-3037-2 |
Package Description: | 1350 PELLET in 1 BOTTLE, GLASS (48951-3037-2) |
NDC Code | 48951-3037-2 |
Proprietary Name | Cartilago Argentum Joint Support |
Package Description | 1350 PELLET in 1 BOTTLE, GLASS (48951-3037-2) |
Product NDC | 48951-3037 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MANDRAGORA OFFICINARUM ROOT BETULA PENDULA LEAF ACONITUM NAPELLUS ROOT ARNICA MONTANA SILVER |
Dosage Form Name | PELLET |
Route Name | ORAL |
Start Marketing Date | 20090901 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Uriel Pharmacy Inc |
Substance Name | ACONITUM NAPELLUS ROOT; ARNICA MONTANA; BETULA PENDULA LEAF; MANDRAGORA OFFICINARUM ROOT; SILVER |
Strength Number | 6; 6; 5; 5; 8 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |