5905. Dermaden. ,(F.D.C. No. 42782. S. No. 42-410 P.) QUANTITY: 2 display ctns., each containing 8 120-cc. btls., and 16 240-cc. btls., at Seattle, Wash. SHIPPED : 9-22-58, from Portland, Oreg., by Consumer Drug Corp. LABEL IN PAST: (Btl.) "Dermaden * * * A Penicillin-Like Skin Application * * * Antibiotic-Anaesthetic-Fungicidal. Distributed by Consumer Drug Cor- poration, Portland, Oregon * * * Contains .01% Diatrex (Disodium-ethylene- diamine-tetracetate), 1% Benzocaine, 1% Salicylic Acid, 1% Resorcin, 2% Methyl Salicylate, 0.5% Phenol, 0.02% Tyrothricin in special greaseless, non- staining, Ultra-Microscopic Base"; (display ctn.) "Dermaden-Fights Fiery Itching, Promotes Healing, Combats Infection * * ?* Contains U-M-B A New Concept in "Sustained Action" Skin Medication * * * in addition to its anti- septic content, the very base of Dermaden is anti-bacterial and absorbs toxins * * * Product of Consumer Drug Corporation." LIBELED : About 1-15-59, W. Dist. Wash. ( CHARGE: 502(a)-when shipped, the labeling contained false and misleading representations that the article was an adequate and effective treatment for inflamed conditions and common skin disorders, including eczema, allergies, nervous itch, and fungus infections; that the action of the article was essentially similar to that of penicillin; and that it represented a new concept in sustained action skin medication; 502(e) (2)-the label failed to bear the common or usual name of each active ingredient since the labeling of the article represented that the ointment base was itself an active ingredient and the label did not disclose the identity of the ointment base or list its ingredients; and 502(f) (2)-the labeling failed to bear such adequate warnings against unsafe dosage or methods or duration of administration in such manner and form as are necessary for the protection of users since its labeling failed to bear a warning in essentially the following form: "Warning: Not for prolonged use. Do not apply to large areas of the body. If redness, irritation, or swelling of the skin develops or pain persists or increases, discontinue use and consult a physician. Do not use in the eyes." DISPOSITION : 5-25-59. Default-destruction.