| Product NDC: | 48951-9998 |
| Proprietary Name: | Saline |
| Non Proprietary Name: | SODIUM CHLORIDE |
| Active Ingredient(s): | 1 [hp_X]/1 & nbsp; SODIUM CHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 48951-9998 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100201 |
| Package NDC: | 48951-9998-1 |
| Package Description: | 10 SOLUTION/ DROPS in 1 BOX (48951-9998-1) |
| NDC Code | 48951-9998-1 |
| Proprietary Name | Saline |
| Package Description | 10 SOLUTION/ DROPS in 1 BOX (48951-9998-1) |
| Product NDC | 48951-9998 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM CHLORIDE |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | [hp_X]/1 |
| Pharmaceutical Classes |