BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH

BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH is an FDA 510(k)-cleared medical device (K101477) manufactured by Glaxosmithkline Consumer Healthcare (Gskch). This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on September 27, 2010.