| Product NDC: | 11673-451 |
| Proprietary Name: | lubricant and redness reliever |
| 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: | 11673-451 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100913 |
| Package NDC: | 11673-451-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (11673-451-15) > 15 mL in 1 BOTTLE, DROPPER |
| NDC Code | 11673-451-15 |
| Proprietary Name | lubricant and redness reliever |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (11673-451-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 11673-451 |
| 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 | Target Corporation |
| Substance Name | NAPHAZOLINE HYDROCHLORIDE; POLYETHYLENE GLYCOL 300 |
| Strength Number | .1; 2 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |