| Product NDC: | 17478-063 |
| Proprietary Name: | Lubricant Eye |
| Non Proprietary Name: | Mineral Oil and Petrolatum |
| Active Ingredient(s): | 120; 880 mg/g; mg/g & nbsp; Mineral Oil and Petrolatum |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17478-063 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930401 |
| Package NDC: | 17478-063-35 |
| Package Description: | 1 TUBE in 1 CARTON (17478-063-35) > 3.5 g in 1 TUBE |
| NDC Code | 17478-063-35 |
| Proprietary Name | Lubricant Eye |
| Package Description | 1 TUBE in 1 CARTON (17478-063-35) > 3.5 g in 1 TUBE |
| Product NDC | 17478-063 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Mineral Oil and Petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19930401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Akorn, Inc. |
| Substance Name | MINERAL OIL; PETROLATUM |
| Strength Number | 120; 880 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |