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Johnson & Johnson achieves 5.9% sales growth in third quarter and raises earnings guidance

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اقرأ بالعربية

Johnson & Johnson announced 5.9% sales growth in the third quarter 2026, adjusted earnings per share of $2.59, and raised its full-year earnings per share guidance to $11.10.

Q3 2026 Reported Sales Growth5.90%
Q3 2026 Operational Sales Growth6.00%
Q3 2026 Adjusted Operational Sales Growth6.10%
Q3 2026 Diluted EPS$0.09
Q3 2026 Adjusted Diluted EPS$2.59
FY2026 Reported Sales Growth Guidance7.40%
FY2026 Adjusted EPS Guidance$11.10
FY2026 Adjusted EPS Growth Guidance2.90%

What this means

Johnson & Johnson continued its growth in the third quarter driven by approximately 6% sales increase, reflecting strong demand for its products. The reported earnings per share of $0.09 is lower due to exceptional accounting items, but adjusted earnings per share of $2.59 provides a clearer picture of operational performance. The company's raise in full-year earnings guidance signals management confidence in sustained positive performance, particularly following new regulatory approvals for important medical products during the quarter.

Details

Johnson & Johnson announced its financial results for the third quarter of 2026, according to the company's filing with regulatory authorities. Sales recorded reported growth of 5.9%, operational growth excluding currency fluctuations of 6.0%, while adjusted operational growth reached 6.1%. Diluted earnings per share (EPS) for the third quarter reached $0.09, while adjusted earnings per share came to $2.59. The significant difference between the two figures is typically attributable to exceptional items such as restructuring charges or legal settlements that do not reflect daily operational performance. On guidance, the company raised its adjusted earnings per share guidance for full-year 2026 by $0.06 to reach $11.10 at the midpoint, representing 2.9% growth. The company also expects full-year reported sales of $101.2 billion at the midpoint, with 7.4% growth. During the third quarter, the company received approval from the U.S. Food and Drug Administration (FDA) to market its OTTAVA robotic surgical system in the United States. Additionally, IMAAVY (nipocalimab-aahu) received FDA approval as the first treatment for warm autoimmune hemolytic anemia (wAIHA), according to the company's filing.

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