| Product NDC: | 59779-408 | 
| Proprietary Name: | Refill Saline Packets | 
| 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) | 
| Product NDC: | 59779-408 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20130401 | 
| Package NDC: | 59779-408-00 | 
| Package Description: | 100 PACKET in 1 CARTON (59779-408-00) > 1 POWDER, FOR SOLUTION in 1 PACKET | 
| NDC Code | 59779-408-00 | 
| Proprietary Name | Refill Saline Packets | 
| Package Description | 100 PACKET in 1 CARTON (59779-408-00) > 1 POWDER, FOR SOLUTION in 1 PACKET | 
| Product NDC | 59779-408 | 
| 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 |