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Sinus Relief - 61727-335-21 - (ASAFETIDA,ECHINACEA ANGUSTIFOLIA,CALCIUM SULFIDE,POTASSIUM DICHROMATE,LUFFA OPERCULATA WHOLE,SILICON DIOXIDE,SINUSITISINUM.)

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Drug Information of Sinus Relief

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)

Labeler Information of Sinus Relief

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 Information of Sinus Relief

Package NDC: 61727-335-21
Package Description: 4 g in 1 TUBE (61727-335-21)

NDC Information of Sinus Relief

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

Complete Information of Sinus Relief


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