Product NDC: | 48951-3102 |
Proprietary Name: | Cinnabar Dandelion Cold Relief |
Non Proprietary Name: | TARAXACUM OFFICINALE ELYMUS REPENS ROOT POTASH MERCURIC SULFIDE |
Active Ingredient(s): | 3; 20; 10; 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; TARAXACUM OFFICINALE ELYMUS REPENS ROOT POTASH MERCURIC SULFIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48951-3102 |
Labeler Name: | Uriel Pharmacy Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090901 |
Package NDC: | 48951-3102-2 |
Package Description: | 1350 PELLET in 1 BOTTLE, GLASS (48951-3102-2) |
NDC Code | 48951-3102-2 |
Proprietary Name | Cinnabar Dandelion Cold Relief |
Package Description | 1350 PELLET in 1 BOTTLE, GLASS (48951-3102-2) |
Product NDC | 48951-3102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TARAXACUM OFFICINALE ELYMUS REPENS ROOT POTASH MERCURIC SULFIDE |
Dosage Form Name | PELLET |
Route Name | ORAL |
Start Marketing Date | 20090901 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Uriel Pharmacy Inc |
Substance Name | ELYMUS REPENS ROOT; MERCURIC SULFIDE; POTASH; TARAXACUM OFFICINALE |
Strength Number | 3; 20; 10; 2 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |