| Product NDC: | 11716-1189 |
| Proprietary Name: | FREDS DRY EYE RELIEF |
| Non Proprietary Name: | GLYCERIN |
| Active Ingredient(s): | .002; .002; .01 mL/mL; mL/mL; mL/mL & nbsp; GLYCERIN |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11716-1189 |
| Labeler Name: | HANLIM PHARM. CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101206 |
| Package NDC: | 11716-1189-9 |
| Package Description: | 1 BOTTLE in 1 CARTON (11716-1189-9) > 15 mL in 1 BOTTLE |
| NDC Code | 11716-1189-9 |
| Proprietary Name | FREDS DRY EYE RELIEF |
| Package Description | 1 BOTTLE in 1 CARTON (11716-1189-9) > 15 mL in 1 BOTTLE |
| Product NDC | 11716-1189 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GLYCERIN |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20101206 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANLIM PHARM. CO., LTD. |
| Substance Name | GLYCERIN; HYPROMELLOSES; POLYETHYLENE GLYCOL 400 |
| Strength Number | .002; .002; .01 |
| Strength Unit | mL/mL; mL/mL; mL/mL |
| Pharmaceutical Classes |