| Product NDC: | 54891-001 |
| Proprietary Name: | Viva |
| Non Proprietary Name: | Polysorbate 80 |
| Active Ingredient(s): | 100 mg/10mL & nbsp; Polysorbate 80 |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54891-001 |
| Labeler Name: | Dakota Laboratories, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19870219 |
| Package NDC: | 54891-001-04 |
| Package Description: | .5 mL in 1 VIAL, SINGLE-USE (54891-001-04) |
| NDC Code | 54891-001-04 |
| Proprietary Name | Viva |
| Package Description | .5 mL in 1 VIAL, SINGLE-USE (54891-001-04) |
| Product NDC | 54891-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polysorbate 80 |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19870219 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dakota Laboratories, LLC |
| Substance Name | POLYSORBATE 80 |
| Strength Number | 100 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes |