Product NDC: | 62011-0100 |
Proprietary Name: | Eye Drops Redness and Dry Eye Relief |
Non Proprietary Name: | Naphazoline hydrochloride, Glycerin |
Active Ingredient(s): | 2; .12 mg/mL; mg/mL & nbsp; Naphazoline hydrochloride, Glycerin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0100 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 62011-0100-1 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (62011-0100-1) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 62011-0100-1 |
Proprietary Name | Eye Drops Redness and Dry Eye Relief |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (62011-0100-1) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 62011-0100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naphazoline hydrochloride, Glycerin |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | McKesson |
Substance Name | GLYCERIN; NAPHAZOLINE HYDROCHLORIDE |
Strength Number | 2; .12 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |