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REFRESH Classic
REFRESH Classic - 0023-0506-01 - (Polyvinyl Alcohol, Povidone)
Drug Information of REFRESH Classic
| Product NDC: | 0023-0506 |
| Proprietary Name: | REFRESH Classic |
| Non Proprietary Name: | Polyvinyl Alcohol, Povidone |
| Active Ingredient(s): | 14; 6 mg/mL; mg/mL & nbsp; Polyvinyl Alcohol, Povidone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REFRESH Classic
| Product NDC: | 0023-0506 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19850912 |
Package Information of REFRESH Classic
| Package NDC: | 0023-0506-01 |
| Package Description: | 30 VIAL, SINGLE-USE in 1 CARTON (0023-0506-01) > .4 mL in 1 VIAL, SINGLE-USE |
NDC Information of REFRESH Classic
| NDC Code | 0023-0506-01 |
| Proprietary Name | REFRESH Classic |
| Package Description | 30 VIAL, SINGLE-USE in 1 CARTON (0023-0506-01) > .4 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0023-0506 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Polyvinyl Alcohol, Povidone |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19850912 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | POLYVINYL ALCOHOL; POVIDONE |
| Strength Number | 14; 6 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
