Product NDC: | 76260-105 |
Proprietary Name: | Aqua Maris Throat |
Non Proprietary Name: | Sodium chloride |
Active Ingredient(s): | 37.5 mg/mL & nbsp; Sodium chloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76260-105 |
Labeler Name: | JGL North America LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20050420 |
Package NDC: | 76260-105-30 |
Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (76260-105-30) > 30 mL in 1 BOTTLE, SPRAY |
NDC Code | 76260-105-30 |
Proprietary Name | Aqua Maris Throat |
Package Description | 1 BOTTLE, SPRAY in 1 CARTON (76260-105-30) > 30 mL in 1 BOTTLE, SPRAY |
Product NDC | 76260-105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium chloride |
Dosage Form Name | SPRAY |
Route Name | ORAL |
Start Marketing Date | 20050420 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | JGL North America LLC |
Substance Name | SODIUM CHLORIDE |
Strength Number | 37.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |