| Product NDC: | 0023-3414 |
| Proprietary Name: | REFRESH REDNESS RELIEF |
| Non Proprietary Name: | phenylephrine hydrochloride, polyvinyl alcohol |
| Active Ingredient(s): | 1.2; 14 mg/mL; mg/mL & nbsp; phenylephrine hydrochloride, polyvinyl alcohol |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0023-3414 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070514 |
| Package NDC: | 0023-3414-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-3414-15) > 15 mL in 1 BOTTLE, DROPPER |
| NDC Code | 0023-3414-15 |
| Proprietary Name | REFRESH REDNESS RELIEF |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-3414-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-3414 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | phenylephrine hydrochloride, polyvinyl alcohol |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20070514 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; POLYVINYL ALCOHOL |
| Strength Number | 1.2; 14 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |