The period following the initial use of ophthalmic solutions is a critical factor influencing their safety and efficacy. Once a container is opened, it becomes susceptible to contamination, and the preservatives within the formulation begin to degrade. This degradation and potential for microbial ingress directly impact the suitability of the product for continued use.
Adhering to recommended disposal timelines minimizes the risk of introducing harmful bacteria or other contaminants into the eye, thereby preventing infections and other adverse reactions. This practice also ensures that the medication retains its intended potency, delivering the expected therapeutic benefit. Historically, varied guidance led to inconsistent practices, underscoring the need for clear and standardized recommendations.
