|
gptkbp:instanceOf
|
gptkb:United_States_federal_law
|
|
gptkbp:administeredBy
|
gptkb:U.S._Food_and_Drug_Administration
|
|
gptkbp:amendedBy
|
gptkb:Dietary_Supplement_Health_and_Education_Act_of_1994
gptkb:Drug_Amendments_of_1962
gptkb:Medical_Device_Amendments_of_1976
|
|
gptkbp:citation
|
21 U.S.C. § 301 et seq.
|
|
gptkbp:country
|
gptkb:United_States
|
|
gptkbp:dateEnacted
|
1938
|
|
gptkbp:enactedBy
|
gptkb:United_States_Congress
|
|
gptkbp:fullName
|
gptkb:Federal_Food,_Drug,_and_Cosmetic_Act
|
|
https://www.w3.org/2000/01/rdf-schema#label
|
FD&C Act
|
|
gptkbp:purpose
|
protect public health
ensure safety and efficacy of drugs
ensure safety of food supply
regulate labeling and advertising
|
|
gptkbp:regulates
|
gptkb:food
cosmetics
drugs
medical devices
radiation-emitting products
biological products
|
|
gptkbp:relatedTo
|
gptkb:Public_Health_Service_Act
gptkb:Food_and_Drug_Administration_Modernization_Act
gptkb:Food_Safety_Modernization_Act
|
|
gptkbp:replacedBy
|
gptkb:Pure_Food_and_Drug_Act_of_1906
|
|
gptkbp:section
|
gptkb:Section_301_(Prohibited_Acts)
gptkb:Section_510(k)_(Premarket_Notification)
Section 505 (New Drug Application)
Section 201 (Definitions)
|
|
gptkbp:bfsParent
|
gptkb:Federal_Food,_Drug,_and_Cosmetic_Act
|
|
gptkbp:bfsLayer
|
6
|