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 |