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Sinus Wash
Sinus Wash - 59779-504-30 - (SODIUM BICARBONATE, SODIUM CHLORIDE)
Drug Information of Sinus Wash
| Product NDC: | 59779-504 |
| Proprietary Name: | Sinus Wash |
| Non Proprietary Name: | SODIUM BICARBONATE, SODIUM CHLORIDE |
| Active Ingredient(s): | 2300; 700 mg/1; mg/1 & nbsp; SODIUM BICARBONATE, SODIUM CHLORIDE |
| Administration Route(s): | NASAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sinus Wash
| Product NDC: | 59779-504 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130401 |
Package Information of Sinus Wash
| Package NDC: | 59779-504-30 |
| Package Description: | 100 PACKET in 1 CARTON (59779-504-30) > 1 POWDER, FOR SOLUTION in 1 PACKET |
NDC Information of Sinus Wash
| NDC Code | 59779-504-30 |
| Proprietary Name | Sinus Wash |
| Package Description | 100 PACKET in 1 CARTON (59779-504-30) > 1 POWDER, FOR SOLUTION in 1 PACKET |
| Product NDC | 59779-504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM BICARBONATE, SODIUM CHLORIDE |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | NASAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CVS Pharmacy |
| Substance Name | SODIUM BICARBONATE; SODIUM CHLORIDE |
| Strength Number | 2300; 700 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
