Product NDC: | 37205-138 |
Proprietary Name: | LEADER RELIEF EYE |
Non Proprietary Name: | TETRAHYDROZOLINE HCL, ZINC SULFATE |
Active Ingredient(s): | .5; 2.5 mg/mL; mg/mL & nbsp; TETRAHYDROZOLINE HCL, ZINC SULFATE |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37205-138 |
Labeler Name: | CARDINAL HEALTH |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120104 |
Package NDC: | 37205-138-05 |
Package Description: | 1 BOTTLE in 1 CARTON (37205-138-05) > 15 mL in 1 BOTTLE |
NDC Code | 37205-138-05 |
Proprietary Name | LEADER RELIEF EYE |
Package Description | 1 BOTTLE in 1 CARTON (37205-138-05) > 15 mL in 1 BOTTLE |
Product NDC | 37205-138 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TETRAHYDROZOLINE HCL, ZINC SULFATE |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20120104 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CARDINAL HEALTH |
Substance Name | TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE |
Strength Number | .5; 2.5 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |