Background/Objectives: Vaccination against herpes zoster (HZ) is an effective strategy in protecting the population against consequences of varicella zoster virus reactivation. Optimal immunogenicity with recombinant zoster vaccine (RZV) relies on completion of the 2-dose series within 2-6 months from the first dose. The objectives of this study were to estimate RZV completion rates and adherence with the recommended administration schedule in the general United States population aged at least 50 years and to evaluate factors influencing completion rates. Methods: Longitudinal, open-source pharmacy and medical claims databases were analyzed for adults aged at least 50 years with a first RZV prescription filled between October 2017 and September 2019. The data were linked to Experian Marketing Services Consumer View data to obtain information regarding race. Completion rates and adherence were calculated overall and stratified according to claim source, age class, sex, and payer type. Logistic regression models were built for each subpopulation of interest to identify factors correlating with completion rates. Results: Overall, cumulative completion rates were 70.41% and 81.80% at 6 and 12 months, respectively. Median time to second dose was approximately 4 months (4.08-5.13 months) and adherence 67.62%. Completion rates were lower in the medical claims database compared with the pharmacy claims database (48.98% vs. 73.23% at 6 months). Regression models confirmed that pharmacy claim was an independent factor for higher completion rates, while African American race and Medicaid Disclosure: Brandon J. Patterson, Lisa I. Glasser, and Philip O. Buck were employees of the GSK group of companies and held shares in the GSK group of companies. Brandon J. Patterson is currently an employee of Janssen Global Services and holds shares in Janssen Global Services. Philip O. Buck is currently an employee of Moderna, Inc and holds shares in Moderna, Inc. Lisa I. Glasser is currently an employee of AstraZeneca and holds shares in AstraZeneca. Siyu Ma is a PostDoc research fellow from Tufts Medical Center and from the GSK group of companies, and declares her institution has received grant support from the GSK group of companies for the conduct of the study. Chi-Chang Chen, Catherine B. McGuiness, and Kainan Sun are employees of IQVIA, which was contracted by the GSK group of companies for the conduct of this study. Catherine B.McGuiness reports holding shares in Pfizer. The authors declare no other financial and non-financial relationships and activities. Funding: This work was supported by GlaxoSmithKline Biologicals SA (Study identifier: HO-18-19056/ VxHO-000052). GlaxoSmithKline Biologicals SA was involved in all stages of study conduct, including analysis of the data. Glax-oSmithKline Biologicals SA also covered all costs associated with the development and publication of this manuscript. Trademarks: Zostavax is a trademark of Merck Sharp & Dohme. Shingrix is a trademark owned by or licensed to the GSK group of companies. Con...