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Aqua Maris Baby
Aqua Maris Baby - 76260-103-15 - (Sodium chloride)
Drug Information of Aqua Maris Baby
| Product NDC: | 76260-103 |
| Proprietary Name: | Aqua Maris Baby |
| Non Proprietary Name: | Sodium chloride |
| Active Ingredient(s): | 11.25 mg/mL & nbsp; Sodium chloride |
| Administration Route(s): | NASAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aqua Maris Baby
| Product NDC: | 76260-103 |
| Labeler Name: | JGL North America LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100708 |
Package Information of Aqua Maris Baby
| Package NDC: | 76260-103-15 |
| Package Description: | 1 BOTTLE, SPRAY in 1 CARTON (76260-103-15) > 15 mL in 1 BOTTLE, SPRAY |
NDC Information of Aqua Maris Baby
| NDC Code | 76260-103-15 |
| Proprietary Name | Aqua Maris Baby |
| Package Description | 1 BOTTLE, SPRAY in 1 CARTON (76260-103-15) > 15 mL in 1 BOTTLE, SPRAY |
| Product NDC | 76260-103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium chloride |
| Dosage Form Name | LIQUID |
| Route Name | NASAL |
| Start Marketing Date | 20100708 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | JGL North America LLC |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 11.25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
