Comparison of Two Daily Disposable Contact Lenses Over 1-week of Wear

Inclusion Criteria: * The subject must be between 18 and 45 years of age (inclusive) with no presbyopic add. * The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form. This should be recorded on the Case Report Form (CRF). * The subject must be willing to wear the study lenses for at least 8 hours per day, 7 days per week. * The subject must be a current successful soft contact lens wearer in both eyes * The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol. * The subject's subjective refraction must result in a vertex corrected spherical contact lens prescription in the range of -1.00D to -6.00D in each eye. * The subject's refractive astigmatism must be less than or equal to 0.75D in both eyes. * The subject must have best corrected visual acuity of 20/30 (6/9) or better in each eye. * The subject must require a visual correction in both eyes (no monofit or monovision allowed). * The subject must have normal eyes with no evidence of abnormality or disease. For the purposes of this study a normal eye is defined as one having: 1. No amblyopia. 2. No evidence of lid abnormality or infection (including blepharitis/meibomitis). 3. No conjunctival abnormality or infection. 4. No clinically significant slit lamp findings (i.e. stromal edema, vascularization, infiltrates or abnormal opacities). 5. No other active ocular disease. Exclusion Criteria: * Any ocular or systemic allergies or diseases that may interfere with contact lens wear. * Any systemic disease, autoimmune disease, or use of medication, which may interfere with contact lens wear. * Clinically significant (Grade 3 or 4) corneal edema, corneal vascularization, corneal staining, or any other abnormalities of the cornea which would contraindicate contact lens wear. * Clinically significant (Grade 3 or 4) tarsal abnormalities or bulbar injection which might interfere with contact lens wear. * Any ocular infection. * Any corneal distortion resulting from previous hard or rigid gas permeable contact lens wear. * Pregnancy or lactation. * No extended wear in the last 3 months. * Diabetes. * Infectious diseases (e.g. hepatitis, tuberculosis) or an immunosuppressive disease (e.g. HIV). * Employee or family member of the staff of the investigational site.