| Product NDC: | 65785-162 |
| Proprietary Name: | PUR-WASH |
| Non Proprietary Name: | Water |
| Active Ingredient(s): | 929 g/946mL & nbsp; Water |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65785-162 |
| Labeler Name: | Niagara Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022305 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110912 |
| Package NDC: | 65785-162-01 |
| Package Description: | 236 mL in 1 BOTTLE, UNIT-DOSE (65785-162-01) |
| NDC Code | 65785-162-01 |
| Proprietary Name | PUR-WASH |
| Package Description | 236 mL in 1 BOTTLE, UNIT-DOSE (65785-162-01) |
| Product NDC | 65785-162 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Water |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110912 |
| Marketing Category Name | NDA |
| Labeler Name | Niagara Pharmaceuticals Inc. |
| Substance Name | WATER |
| Strength Number | 929 |
| Strength Unit | g/946mL |
| Pharmaceutical Classes |