Product NDC: | 62011-0104 |
Proprietary Name: | Eye Drops Advanced Relief |
Non Proprietary Name: | Tetrahydrozoline hydrochloride, Polyethylene glycol 400, Dextran 70, Povidone |
Active Ingredient(s): | 1; 10; 10; .5 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Tetrahydrozoline hydrochloride, Polyethylene glycol 400, Dextran 70, Povidone |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0104 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 62011-0104-1 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (62011-0104-1) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 62011-0104-1 |
Proprietary Name | Eye Drops Advanced Relief |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (62011-0104-1) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 62011-0104 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tetrahydrozoline hydrochloride, Polyethylene glycol 400, Dextran 70, Povidone |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | DEXTRAN 70; POLYETHYLENE GLYCOL 400; POVIDONE; TETRAHYDROZOLINE HYDROCHLORIDE |
Strength Number | 1; 10; 10; .5 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |