Product NDC: | 61727-335 |
Proprietary Name: | Sinus Relief |
Non Proprietary Name: | ASAFETIDA,ECHINACEA ANGUSTIFOLIA,CALCIUM SULFIDE,POTASSIUM DICHROMATE,LUFFA OPERCULATA WHOLE,SILICON DIOXIDE,SINUSITISINUM. |
Active Ingredient(s): | 8; 8; 12; 9; 18; 10; 18 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_C]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g & nbsp; ASAFETIDA,ECHINACEA ANGUSTIFOLIA,CALCIUM SULFIDE,POTASSIUM DICHROMATE,LUFFA OPERCULATA WHOLE,SILICON DIOXIDE,SINUSITISINUM. |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61727-335 |
Labeler Name: | Homeocare Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120724 |
Package NDC: | 61727-335-21 |
Package Description: | 4 g in 1 TUBE (61727-335-21) |
NDC Code | 61727-335-21 |
Proprietary Name | Sinus Relief |
Package Description | 4 g in 1 TUBE (61727-335-21) |
Product NDC | 61727-335 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ASAFETIDA,ECHINACEA ANGUSTIFOLIA,CALCIUM SULFIDE,POTASSIUM DICHROMATE,LUFFA OPERCULATA WHOLE,SILICON DIOXIDE,SINUSITISINUM. |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20120724 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Homeocare Laboratories |
Substance Name | ASAFETIDA; CALCIUM SULFIDE; ECHINACEA ANGUSTIFOLIA; LUFFA OPERCULATA WHOLE; POTASSIUM DICHROMATE; SILICON DIOXIDE; SINUSITISINUM |
Strength Number | 8; 8; 12; 9; 18; 10; 18 |
Strength Unit | [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_C]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g |
Pharmaceutical Classes |