| Product NDC: | 53799-240 |
| Proprietary Name: | Sinus Relief |
| Non Proprietary Name: | Kali bichromicum, Luffa operculata, Sabadilla |
| Active Ingredient(s): | 6; 6; 6 [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL & nbsp; Kali bichromicum, Luffa operculata, Sabadilla |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53799-240 |
| Labeler Name: | Similasan AG |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20101201 |
| Package NDC: | 53799-240-20 |
| Package Description: | 20 mL in 1 BOTTLE, SPRAY (53799-240-20) |
| NDC Code | 53799-240-20 |
| Proprietary Name | Sinus Relief |
| Package Description | 20 mL in 1 BOTTLE, SPRAY (53799-240-20) |
| Product NDC | 53799-240 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Kali bichromicum, Luffa operculata, Sabadilla |
| Dosage Form Name | SPRAY |
| Route Name | NASAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Similasan AG |
| Substance Name | LUFFA OPERCULATA FRUIT; POTASSIUM DICHROMATE; SCHOENOCAULON OFFICINALE SEED |
| Strength Number | 6; 6; 6 |
| Strength Unit | [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL |
| Pharmaceutical Classes |