the food and drug administration (fda) is proposing to amend the regulations to require all medical devices containing natural rubber latex that may directly or indirectly contact living human tissue to be labeled with a statement identifying the. each required labeling statement shall be prominently and legibly displayed in conformance with section 502(c) of the federal food, drug, and cosmetic act (the act) (21 u.). the fda is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices and by ensuring the. Medications acetaminophen (tylenol), 160mg5ml oral suspension 1 bottle 1 bottle albuterol, 2. 5mg3ml unit dose ampule 2 2 albuterolipratropium (duo-neb), 2. 5mg in 3ml unit dose ampule (squads may also choose to carry albuterol and ipratropium bromide individually and mix them per the optional medication list m.). Latex in drug vial stoppers - adamson - 2014 - best law the day at www. Com law details feb 18, 2014 we believe there should be an easily accessible, contemporary database detailing the latex content of injectable drugs used in the uk. Currently, this does not exist, although the injectable medicines guide ( www.). Medication administration 16 emergency medications 16 airway management, respirations and artificial ventilation 17 airway management 17 respiration 18 artificial ventilation 18 assessment 19 scene size-up 19 primary assessment 20 history taking 20 secondary assessment 20 monitoring devices 21 reassessment 21. Ment, through its food and drug administration (fda), is responsible for implementing and enforcing the federal food, drug, and cosmetic act. The fda is responsible for the control and prevention of misbranding and of adultera-tion of food, drugs, and cosmetics moving in interstate com-merce.