Product NDC: | 24208-349 |
Proprietary Name: | Advanced Eye Relief/ Redness Instant Relief |
Non Proprietary Name: | Naphazoline Hydrochloride and Polyethylene glycol 300 |
Active Ingredient(s): | .1; 2 mg/mL; mg/mL & nbsp; Naphazoline Hydrochloride and Polyethylene glycol 300 |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24208-349 |
Labeler Name: | Bausch & Lomb Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part349 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100913 |
Package NDC: | 24208-349-75 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-349-75) > 15 mL in 1 BOTTLE, DROPPER |
NDC Code | 24208-349-75 |
Proprietary Name | Advanced Eye Relief/ Redness Instant Relief |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-349-75) > 15 mL in 1 BOTTLE, DROPPER |
Product NDC | 24208-349 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naphazoline Hydrochloride and Polyethylene glycol 300 |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 20100913 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | NAPHAZOLINE HYDROCHLORIDE; POLYETHYLENE GLYCOL 300 |
Strength Number | .1; 2 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |