Product Images Phenylephrine Hydrochloride

This is a description of an ophthalmic solution containing Phenylephrine Hydrochloride for topical application in the eye, provided in a bottle with a proper drop control. The user should not use the solution if the imprinted seal is broken or missing, and after opening, the solution can be used until the expiration date indicated on the bottle. Each milliliter of the solution includes 2.5% Phenylephrine Hydrochloride and Benzalkonium Chloride as a preservative. The package should be stored in a tightly closed container at temperatures between 20-25 °C. It is important not to use the product if the solution appears brown or contains a precipitate. The information for a correct dosage is located in the package insert. The product was distributed by Akorn, Gurnee, IL 60031, labeled with an NDC code 17478-201-02, and a Lot and EXP number are also available.*

This is a description of a medication packaging for Phenylephrine Hydrochloride Ophthalmic Solution. It is for topical use only and is not meant for injection. The solution is available in a 2mL container and contains 25mg of Phenylephrine Hydrochloride as an active ingredient. Other ingredients present are Benzalkonium Chloride 0.1mg, Sodium Phosphate Dibasic, Sodium Phosphate Monobasic, Sodium Hydroxide, and/or Phosphoric Acid may be added to adjust pH (4.0 to 7.5) and Water for Injection q.5. Except when necessary to adjust pH, its usage instructions state that solution should be kept tight and away from excessive heat. The medicine should not be used if the solution is brown or has any discoloration. The packaging warns users to keep the medication away from children and to not use this medication if the imprinted seal is broken or missing. For precise dosage appropriate, users are advised to check the package insert. It is distributed by Akorn Operating Company LLC, located at Gurnee, Illinois.*

This is a description of a medication containing Phenylephrine for topical eye application. The medication is distributed by Akorn Operating Company LLC and each mL of the solution contains 0.1 mg (0.01%) of Chloride. Usual dosage instructions are on the package, and the medication should not be used if the solution has precipitated or the seal is broken. The container should be kept tightly closed and out of reach of children.*