196.100. 1. Any manufacturer, packer, distributor or seller of drugsor devices in this state shall comply with the current federal labelingrequirements contained in the Federal Food, Drug and Cosmetic Act, asamended, and any federal regulations promulgated thereunder. Any drug ordevice which contains labeling that is not in compliance with theprovisions of this section shall be deemed misbranded.
2. A drug dispensed on a written prescription signed by a licensedphysician, dentist, or veterinarian, except a drug dispensed in the courseof the conduct of a business of dispensing drugs pursuant to a diagnosis bymail, shall be exempt from the requirements of this section if suchphysician, dentist, or veterinarian is licensed by law to administer suchdrug, and such drug bears a label containing the name and place of businessof the dispenser, the serial number and date of such prescription, and thename of such physician, dentist, or veterinarian.
3. The department is hereby directed to promulgate regulationsexempting from any labeling or packaging requirement of sections 196.010 to196.120, drugs and devices which are, in accordance with the practice ofthe trade, to be processed, labeled, or repacked in substantial quantitiesat establishments other than those where originally processed or packed, oncondition that such drugs and devices are not adulterated or misbrandedunder the provisions of said sections upon removal from such processing,labeling, or repacking establishment.
(L. 1943 p. 559 § 9870, A.L. 2001 H.B. 796 merged with S.B. 514)
196.100. 1. Any manufacturer, packer, distributor or seller of drugsor devices in this state shall comply with the current federal labelingrequirements contained in the Federal Food, Drug and Cosmetic Act, asamended, and any federal regulations promulgated thereunder. Any drug ordevice which contains labeling that is not in compliance with theprovisions of this section shall be deemed misbranded.
2. A drug dispensed on a written prescription signed by a licensedphysician, dentist, or veterinarian, except a drug dispensed in the courseof the conduct of a business of dispensing drugs pursuant to a diagnosis bymail, shall be exempt from the requirements of this section if suchphysician, dentist, or veterinarian is licensed by law to administer suchdrug, and such drug bears a label containing the name and place of businessof the dispenser, the serial number and date of such prescription, and thename of such physician, dentist, or veterinarian.
3. The department is hereby directed to promulgate regulationsexempting from any labeling or packaging requirement of sections 196.010 to196.120, drugs and devices which are, in accordance with the practice ofthe trade, to be processed, labeled, or repacked in substantial quantitiesat establishments other than those where originally processed or packed, oncondition that such drugs and devices are not adulterated or misbrandedunder the provisions of said sections upon removal from such processing,labeling, or repacking establishment.
(L. 1943 p. 559 § 9870, A.L. 2001 H.B. 796 merged with S.B. 514)
196.100. 1. Any manufacturer, packer, distributor or seller of drugsor devices in this state shall comply with the current federal labelingrequirements contained in the Federal Food, Drug and Cosmetic Act, asamended, and any federal regulations promulgated thereunder. Any drug ordevice which contains labeling that is not in compliance with theprovisions of this section shall be deemed misbranded.
2. A drug dispensed on a written prescription signed by a licensedphysician, dentist, or veterinarian, except a drug dispensed in the courseof the conduct of a business of dispensing drugs pursuant to a diagnosis bymail, shall be exempt from the requirements of this section if suchphysician, dentist, or veterinarian is licensed by law to administer suchdrug, and such drug bears a label containing the name and place of businessof the dispenser, the serial number and date of such prescription, and thename of such physician, dentist, or veterinarian.
3. The department is hereby directed to promulgate regulationsexempting from any labeling or packaging requirement of sections 196.010 to196.120, drugs and devices which are, in accordance with the practice ofthe trade, to be processed, labeled, or repacked in substantial quantitiesat establishments other than those where originally processed or packed, oncondition that such drugs and devices are not adulterated or misbrandedunder the provisions of said sections upon removal from such processing,labeling, or repacking establishment.
(L. 1943 p. 559 § 9870, A.L. 2001 H.B. 796 merged with S.B. 514)
