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Advanced Eye Relief/ Redness Maximum Relief
Advanced Eye Relief/ Redness Maximum Relief - 24208-450-15 - (Naphazoline Hydrochloride and Hypromellose)
Drug Information of Advanced Eye Relief/ Redness Maximum Relief
| Product NDC: | 24208-450 |
| Proprietary Name: | Advanced Eye Relief/ Redness Maximum Relief |
| Non Proprietary Name: | Naphazoline Hydrochloride and Hypromellose |
| Active Ingredient(s): | .3; 5 mg/mL; mg/mL & nbsp; Naphazoline Hydrochloride and Hypromellose |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advanced Eye Relief/ Redness Maximum Relief
| Product NDC: | 24208-450 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100902 |
Package Information of Advanced Eye Relief/ Redness Maximum Relief
| Package NDC: | 24208-450-15 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-450-15) > 15 mL in 1 BOTTLE, DROPPER |
NDC Information of Advanced Eye Relief/ Redness Maximum Relief
| NDC Code | 24208-450-15 |
| Proprietary Name | Advanced Eye Relief/ Redness Maximum Relief |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-450-15) > 15 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-450 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naphazoline Hydrochloride and Hypromellose |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20100902 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | HYPROMELLOSE; NAPHAZOLINE HYDROCHLORIDE |
| Strength Number | .3; 5 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
