| 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 |