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 |