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 |