| Product NDC: | 54799-917 |
| Proprietary Name: | retaine MGD |
| Non Proprietary Name: | Mineral Oil |
| Active Ingredient(s): | .002; .002 mL/.4mL; mL/.4mL & nbsp; Mineral Oil |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54799-917 |
| Labeler Name: | OCuSOFT, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120105 |
| Package NDC: | 54799-917-30 |
| Package Description: | 30 VIAL, SINGLE-DOSE in 1 CONTAINER (54799-917-30) > .4 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 54799-917-30 |
| Proprietary Name | retaine MGD |
| Package Description | 30 VIAL, SINGLE-DOSE in 1 CONTAINER (54799-917-30) > .4 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 54799-917 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Mineral Oil |
| Dosage Form Name | EMULSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | OCuSOFT, Inc. |
| Substance Name | LIGHT MINERAL OIL; MINERAL OIL |
| Strength Number | .002; .002 |
| Strength Unit | mL/.4mL; mL/.4mL |
| Pharmaceutical Classes |