| Product NDC: | 0363-0307 |
| Proprietary Name: | Lubricant Eye |
| Non Proprietary Name: | Polyethylene Glycol 400 and Propylene Glycol |
| Active Ingredient(s): | 4; 3 mg/mL; mg/mL & nbsp; Polyethylene Glycol 400 and Propylene Glycol |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0363-0307 |
| Labeler Name: | Walgreens |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130426 |
| Package NDC: | 0363-0307-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0363-0307-02) > 10 mL in 1 BOTTLE, DROPPER |
| NDC Code | 0363-0307-02 |
| Proprietary Name | Lubricant Eye |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0363-0307-02) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0363-0307 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polyethylene Glycol 400 and Propylene Glycol |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130426 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Walgreens |
| Substance Name | POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL |
| Strength Number | 4; 3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |