Product NDC: | 67172-898 |
Proprietary Name: | Clear Eyes Triple Action |
Non Proprietary Name: | Polyvinyl Alcohol and Povidone and Tetrahydrozoline Hydrochloride |
Active Ingredient(s): | .00125; .0015; .000125 mL/mL; mL/mL; mL/mL & nbsp; Polyvinyl Alcohol and Povidone and Tetrahydrozoline Hydrochloride |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67172-898 |
Labeler Name: | Prestige Brands Holdings, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110315 |
Package NDC: | 67172-898-01 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOX (67172-898-01) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 67172-898-01 |
Proprietary Name | Clear Eyes Triple Action |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (67172-898-01) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 67172-898 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Polyvinyl Alcohol and Povidone and Tetrahydrozoline Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | OPHTHALMIC |
Start Marketing Date | 20110315 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Prestige Brands Holdings, Inc. |
Substance Name | POLYVINYL ALCOHOL; POVIDONE; TETRAHYDROZOLINE HYDROCHLORIDE |
Strength Number | .00125; .0015; .000125 |
Strength Unit | mL/mL; mL/mL; mL/mL |
Pharmaceutical Classes |