 
                        | Product NDC: | 10655-1944 | 
| Proprietary Name: | Nasosol Saline | 
| Non Proprietary Name: | SODIUM CHLORIDE | 
| Active Ingredient(s): | 3 mL/100mL & nbsp; SODIUM CHLORIDE | 
| Administration Route(s): | NASAL | 
| Dosage Form(s): | SPRAY | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 10655-1944 | 
| Labeler Name: | Benton Therapeutics, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20110111 | 
| Package NDC: | 10655-1944-0 | 
| Package Description: | 100 mL in 1 BOTTLE, SPRAY (10655-1944-0) | 
| NDC Code | 10655-1944-0 | 
| Proprietary Name | Nasosol Saline | 
| Package Description | 100 mL in 1 BOTTLE, SPRAY (10655-1944-0) | 
| Product NDC | 10655-1944 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | SODIUM CHLORIDE | 
| Dosage Form Name | SPRAY | 
| Route Name | NASAL | 
| Start Marketing Date | 20110111 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Benton Therapeutics, Inc. | 
| Substance Name | SODIUM CHLORIDE | 
| Strength Number | 3 | 
| Strength Unit | mL/100mL | 
| Pharmaceutical Classes |