A Study of Ibuprofen (IBU) 250mg/APAP 500mg In The Treatment Of Post-Surgical Dental Pain

Inclusion Criteria

1. Males and females 18 years to 40 years of age (inclusive).

2. Outpatients who have undergone surgical extraction of 3 or more third molars, of which
at least 2 must be a partial or complete bony mandibular impaction.

3. Subject must have at least moderate pain on the 4 point categorical scale, confirmed
by at least 50 mm on the 100 mm VAS PSR scale within approximately 5 hours (ie, less
than or equal to 5 hours, 15 minutes) after surgery is completed.

4. In general good health and have no contraindications to the study or rescue
medication.

Exclusion Criteria

1. Presence or history of any significant hepatic, renal, endocrine, cardiovascular,
neurological, psychiatric, gastrointestinal, pulmonary, hematologic, or metabolic
disorder determined by the Investigator to place the subject at increased risk,
including the presence or history within 2 years of screening of the following medical
conditions/disorders:

- Gastrointestinal ulcer or gastrointestinal bleeding;

- Paralytic ileus or other gastrointestinal obstructive disorders;

- Bleeding disorder.

2. Hypersensitivity to ibuprofen, naproxen, aspirin, or any other NSAID; or to APAP,
tramadol, other opioids, or to their combinations.

3. Prior use of any type of analgesic or NSAID within five half lives of that drug or
less before taking the first dose of investigational product, except for pre
anesthetic medication and anesthesia for the procedure.