OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for AKTEN ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use Initial U.S. Approval: 1972
lidocaine hydrochloride 0.035 MG/MG Ophthalmic Gel
SCD
15
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for AKTEN ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use Initial U.S. Approval: 1972
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for AKTEN ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use Initial U.S. Approval: 1972
lidocaine hydrochloride 0.035 MG/MG Ophthalmic Gel
SCD
9
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for Akten ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use. Initial U.S. Approval: 1972
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for Akten ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use. Initial U.S. Approval: 1972
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for Akten ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use. Initial U.S. Approval: 1972
These highlights do not include all the information needed to use AKTEN ® safely and effectively. See full prescribing information for AKTEN ® . AKTEN ® (lidocaine hydrochloride ophthalmic gel), for topical ophthalmic use Initial U.S. Approval: 1972