| 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 |