Product NDC: | 17478-062 |
Proprietary Name: | Artificial Tear |
Non Proprietary Name: | Lanolin, Mineral Oil, Petrolatum |
Active Ingredient(s): | 20; 150; 830 mg/g; mg/g; mg/g & nbsp; Lanolin, Mineral Oil, Petrolatum |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-062 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19900901 |
Package NDC: | 17478-062-35 |
Package Description: | 1 TUBE in 1 CARTON (17478-062-35) > 3.5 g in 1 TUBE |
NDC Code | 17478-062-35 |
Proprietary Name | Artificial Tear |
Package Description | 1 TUBE in 1 CARTON (17478-062-35) > 3.5 g in 1 TUBE |
Product NDC | 17478-062 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Lanolin, Mineral Oil, Petrolatum |
Dosage Form Name | OINTMENT |
Route Name | OPHTHALMIC |
Start Marketing Date | 19900901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Akorn, Inc. |
Substance Name | LANOLIN; MINERAL OIL; PETROLATUM |
Strength Number | 20; 150; 830 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes |