Product NDC: | 50169-0002 |
Proprietary Name: | Type 3 Sinus Regular |
Non Proprietary Name: | Silicea, Hydrastis Canadensis, Kali Bichromicum, Calcarea Carbonica |
Active Ingredient(s): | 6; 12; 6; 6 [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg & nbsp; Silicea, Hydrastis Canadensis, Kali Bichromicum, Calcarea Carbonica |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50169-0002 |
Labeler Name: | T Gone Remedies |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130403 |
Package NDC: | 50169-0002-1 |
Package Description: | 15000 mg in 1 BOTTLE (50169-0002-1) |
NDC Code | 50169-0002-1 |
Proprietary Name | Type 3 Sinus Regular |
Package Description | 15000 mg in 1 BOTTLE (50169-0002-1) |
Product NDC | 50169-0002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Silicea, Hydrastis Canadensis, Kali Bichromicum, Calcarea Carbonica |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20130403 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | T Gone Remedies |
Substance Name | GOLDENSEAL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM DICHROMATE; SILICON DIOXIDE |
Strength Number | 6; 12; 6; 6 |
Strength Unit | [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg |
Pharmaceutical Classes |