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 |