Background: This study sought to determine whether the antioxidant effects of astaxanthin (AST) could have an anti-inflammatory effect to reduce inflammation caused by atopic dermatitis (AD).Methods: Using a mouse model of AD induced by phtalic acid (PA), the levels of inflammation, inflammatory agents, and evidence of antioxidant activity were examined in PA treated mice (n = 3), PA-AST treated mice (n = 3), and a control group of mice (n = 3). This included measurements of ear thickness, levels of mast cells, IgE, inflammatory cytokine, malondialdehyde (MDA), hydrogen peroxide, HO-1, and GPx-1.Results: AST treatment significantly prevented inflammation as measured by ear thickness (<i>p</i> < 0.05), mast cell count (<i>p</i> < 0.001), and IgE concentration in the blood (<i>p</i> < 0.001). Levels of TNF-α (<i>p</i> < 0.001), IL-1β (<i>p</i> < 0.001), IL-6 (<i>p</i> < 0.001), and MDA (<i>p</i> < 0.05) were also significantly lower. In addition, GSH levels increased significantly (<i>p</i> < 0.001), and the level of hydrogen peroxide significantly reduced (<i>p</i> < 0.01). The expression of HO-1, GPx-1 increased.Conclusion: In this small experimental study, AST acted on inflammatory mechanisms that induced AD, through anti-inflammatory and antioxidant mechanisms, and is a candidate of interest in the clinical treatment of AD.