| Product NDC: | 57520-0426 | 
| Proprietary Name: | Type 3 Sinus Max | 
| Non Proprietary Name: | Calcarea carbonica, Hydrastis canadensis, Kali bichromicum, Silicea, | 
| Active Ingredient(s): | 200; 200; 200; 200 [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg & nbsp; Calcarea carbonica, Hydrastis canadensis, Kali bichromicum, Silicea, | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 57520-0426 | 
| Labeler Name: | Apotheca Company | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC | 
| Start Marketing Date: | 20100714 | 
| Package NDC: | 57520-0426-1 | 
| Package Description: | 15000 mg in 1 BOTTLE (57520-0426-1) | 
| NDC Code | 57520-0426-1 | 
| Proprietary Name | Type 3 Sinus Max | 
| Package Description | 15000 mg in 1 BOTTLE (57520-0426-1) | 
| Product NDC | 57520-0426 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Calcarea carbonica, Hydrastis canadensis, Kali bichromicum, Silicea, | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20100714 | 
| Marketing Category Name | UNAPPROVED HOMEOPATHIC | 
| Labeler Name | Apotheca Company | 
| Substance Name | GOLDENSEAL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM DICHROMATE; SILICON DIOXIDE | 
| Strength Number | 200; 200; 200; 200 | 
| Strength Unit | [hp_C]/mg; [hp_C]/mg; [hp_C]/mg; [hp_C]/mg | 
| Pharmaceutical Classes |