Product NDC: | 52429-123 |
Proprietary Name: | NasalAsalt |
Non Proprietary Name: | Sodium Chloride |
Active Ingredient(s): | 2600 mg/100mL & nbsp; Sodium Chloride |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52429-123 |
Labeler Name: | Nasal and Sinus Health, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111101 |
Package NDC: | 52429-123-01 |
Package Description: | 1 CANISTER in 1 BOX (52429-123-01) > 100 mL in 1 CANISTER |
NDC Code | 52429-123-01 |
Proprietary Name | NasalAsalt |
Package Description | 1 CANISTER in 1 BOX (52429-123-01) > 100 mL in 1 CANISTER |
Product NDC | 52429-123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Chloride |
Dosage Form Name | SPRAY |
Route Name | NASAL |
Start Marketing Date | 20111101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Nasal and Sinus Health, Inc. |
Substance Name | SODIUM CHLORIDE |
Strength Number | 2600 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |