The study is no longer required due to change in development program strategy.

The purpose of this study is to evaluate the safety of a fixed combination of acetaminophen/naproxen sodium when administered as multiple doses over a period of up to 10 days in adolescents 12 to below 17 years of age with post-procedure orthodontic pain.

Inclusion Criteria:

• Weigh 72 pounds or greater and have a body mass index (BMI)-for-age between the 5th and 95th percentile (inclusive) at Screening
• Have undergone an orthodontic procedure within 4 hours prior to baseline (enrollment) visit
• Females of childbearing potential and males agree to the contraceptive requirements of study

Exclusion Criteria:

• Are female and are pregnant, breastfeeding, or trying to become pregnant or male with a pregnant partner or a partner currently trying to become pregnant
• Have a positive urine drug test on screening or enrollment
• Are not able to swallow whole tablets or capsules
• Arrive at the site on the day of enrollment with motion sickness and/or have a history of frequent motion sickness (car sickness) in the past year, which in the judgement of the investigator is likely to confound assessment of adverse events
• Routinely use oral analgesics greater than or equal to (>=) 5 times per week
• Have a known allergy or hypersensitivity to naproxen (or other nonsteroidal anti-inflammatory drugs including aspirin) or acetaminophen or have asthma
• Have presence or a history of major medical condition that in the Investigator's opinion may jeopardize the participant's safety or wellbeing or the integrity of the study
• Have a history of chronic use of tranquilizers, alcohol, tobacco/vaping, or substance abuse, as judged by the Investigator site staff, in the last year
• Have a history of endoscopically documented peptic ulcer disease or bleeding disorder in the last two years
• Have a diagnosis of gastroesophageal reflux disorder, or experienced frequent heartburn in the past year

Johnson & Johnson Consumer Inc. has an agreement with the Yale Open Data Access (YODA) Project to serve as the independent review panel for evaluation of requests for clinical study reports and participant level data from investigators and physicians for scientific research that will advance medical knowledge and public health. Requests for access to the study data can be submitted through the YODA Project site at http://yoda.yale.edu