| Part 1
|
General Enforcement Regulations |
| Part 2
|
General Administrative Rulings And Decisions |
| Part 3
|
Product Jurisdiction |
| Part 4
|
Regulation Of Combination Products |
| Part 5
|
Organization |
| Part 7
|
Enforcement Policy |
| Part 10
|
Administrative Practices And Procedures |
| Part 11
|
Electronic Records; Electronic Signatures |
| Part 12
|
Formal Evidentiary Public Hearing |
| Part 13
|
Public Hearing Before A Public Board Of Inquiry |
| Part 14
|
Public Hearing Before A Public Advisory Committee |
| Part 15
|
Public Hearing Before The Commissioner |
| Part 16
|
Regulatory Hearing Before The Food And Drug Administration |
| Part 17
|
Civil Money Penalties Hearings |
| Part 19
|
Standards Of Conduct And Conflicts Of Interest |
| Part 20
|
Public Information |
| Part 21
|
Protection Of Privacy |
| Part 25
|
Environmental Impact Considerations |
| Part 26
|
Mutual Recognition Of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, And Certain Medical Device Product Evaluation Reports: United States And The European Community |
| Part 50
|
Protection Of Human Subjects |
| Part 54
|
Financial Disclosure By Clinical Investigators |
| Part 56
|
Institutional Review Boards |
| Part 58
|
Good Laboratory Practice For Nonclinical Laboratory Studies |
| Part 60
|
Patent Term Restoration |
| Part 70
|
Color Additives |
| Part 71
|
Color Additive Petitions |
| Part 73
|
Listing Of Color Additives Exempt From Certification |
| Part 74
|
Listing Of Color Additives Subject To Certification |
| Part 80
|
Color Additive Certification |
| Part 81
|
General Specifications And General Restrictions For Provisional Color Additives For Use In Foods, Drugs, And Cosmetics |
| Part 82
|
Listing Of Certified Provisionally Listed Colors And Specifications |
| Part 99
|
Dissemination Of Information On Unapproved/New Uses For Marketed Drugs, Biologics, And Devices |
| Part 100
|
General |
| Part 101
|
Food Labeling |
| Part 102
|
Common Or Usual Name For Nonstandardized Foods |
| Part 104
|
Nutritional Quality Guidelines For Foods |
| Part 105
|
Foods For Special Dietary Use |
| Part 106
|
Infant Formula Requirements Pertaining To Current Good Manufacturing Practice, Quality Control Procedures, Quality Factors, Records And Reports, And Notifications |
| Part 107
|
Infant Formula |
| Part 108
|
Emergency Permit Control |
| Part 109
|
Unavoidable Contaminants In Food For Human Consumption And Food-Packaging Material |
| Part 110
|
Current Good Manufacturing Practice In Manufacturing, Packing, Or Holding Human Food |
| Part 111
|
Current Good Manufacturing Practice In Manufacturing, Packaging, Labeling, Or Holding Operations For Dietary Supplements |
| Part 113
|
Thermally Processed Low-Acid Foods Packaged In Hermetically Sealed Containers |
| Part 114
|
Acidified Foods |
| Part 115
|
Shell Eggs |
| Part 118
|
Production, Storage, And Transportation Of Shell Eggs |
| Part 119
|
Dietary Supplements That Present A Significant Or Unreasonable Risk |
| Part 120
|
Hazard Analysis And Critical Control Point (Haccp) Systems |
| Part 123
|
Fish And Fishery Products |
| Part 129
|
Processing And Bottling Of Bottled Drinking Water |
| Part 130
|
Food Standards: General |
| Part 131
|
Milk And Cream |
| Part 133
|
Cheeses And Related Cheese Products |
| Part 135
|
Frozen Desserts |
| Part 136
|
Bakery Products |
| Part 137
|
Cereal Flours And Related Products |
| Part 139
|
Macaroni And Noodle Products |
| Part 145
|
Canned Fruits |
| Part 146
|
Canned Fruit Juices |
| Part 150
|
Fruit Butters, Jellies, Preserves, And Related Products |
| Part 152
|
Fruit Pies |
| Part 155
|
Canned Vegetables |
| Part 156
|
Vegetable Juices |
| Part 158
|
Frozen Vegetables |
| Part 160
|
Eggs And Egg Products |
| Part 161
|
Fish And Shellfish |
| Part 163
|
Cacao Products |
| Part 164
|
Tree Nut And Peanut Products |
| Part 165
|
Beverages |
| Part 166
|
Margarine |
| Part 168
|
Sweeteners And Table Sirups |
| Part 169
|
Food Dressings And Flavorings |
| Part 170
|
Food Additives |
| Part 171
|
Food Additive Petitions |
| Part 172
|
Food Additives Permitted For Direct Addition To Food For Human Consumption |
| Part 173
|
Secondary Direct Food Additives Permitted In Food For Human Consumption |
| Part 174
|
Indirect Food Additives: General |
| Part 175
|
Indirect Food Additives: Adhesives And Components Of Coatings |
| Part 176
|
Indirect Food Additives: Paper And Paperboard Components |
| Part 177
|
Indirect Food Additives: Polymers |
| Part 178
|
Indirect Food Additives: Adjuvants, Production Aids, And Sanitizers |
| Part 179
|
Irradiation In The Production, Processing And Handling Of Food |
| Part 180
|
Food Additives Permitted In Food Or In Contact With Food On An Interim Basis Pending Additional Study |
| Part 181
|
Prior-Sanctioned Food Ingredients |
| Part 182
|
Substances Generally Recognized As Safe |
| Part 184
|
Direct Food Substances Affirmed As Generally Recognized As Safe |
| Part 186
|
Indirect Food Substances Affirmed As Generally Recognized As Safe |
| Part 189
|
Substances Prohibited From Use In Human Food |
| Part 190
|
Dietary Supplements |
| Part 200
|
General |
| Part 201
|
Labeling |
| Part 202
|
Prescription Drug Advertising |
| Part 203
|
Prescription Drug Marketing |
| Part 205
|
Guidelines For State Licensing Of Wholesale Prescription Drug Distributors |
| Part 206
|
Imprinting Of Solid Oral Dosage Form Drug Products For Human Use |
| Part 207
|
Registration Of Producers Of Drugs And Listing Of Drugs In Commercial Distribution |
| Part 208
|
Medication Guides For Prescription Drug Products |
| Part 209
|
Requirement For Authorized Dispensers And Pharmacies To Distribute A Side Effects Statement |
| Part 210
|
Current Good Manufacturing Practice In Manufacturing, Processing, Packing, Or Holding Of Drugs; General |
| Part 211
|
Current Good Manufacturing Practice For Finished Pharmaceuticals |
| Part 212
|
Current Good Manufacturing Practice For Positron Emission Tomography Drugs |
| Part 216
|
Pharmacy Compounding |
| Part 225
|
Current Good Manufacturing Practice For Medicated Feeds |
| Part 226
|
Current Good Manufacturing Practice For Type A Medicated Articles |
| Part 250
|
Special Requirements For Specific Human Drugs |
| Part 290
|
Controlled Drugs |
| Part 299
|
Drugs; Official Names And Established Names |
| Part 300
|
General |
| Part 310
|
New Drugs |
| Part 312
|
Investigational New Drug Application |
| Part 314
|
Applications For Fda Approval To Market A New Drug |
| Part 315
|
Diagnostic Radiopharmaceuticals |
| Part 316
|
Orphan Drugs |
| Part 317
|
Qualifying Pathogens |
| Part 320
|
Bioavailability And Bioequivalence Requirements |
| Part 328
|
Over-The-Counter Drug Products Intended For Oral Ingestion That Contain Alcohol |
| Part 329
|
Nonprescription Human Drug Products Subject To Section 760 Of The Federal Food, Drug, And Cosmetic Act |
| Part 330
|
Over-The-Counter (Otc) Human Drugs Which Are Generally Recognized As Safe And Effective And Not Misbranded |
| Part 331
|
Antacid Products For Over-The-Counter (Otc) Human Use |
| Part 332
|
Antiflatulent Products For Over-The-Counter Human Use |
| Part 333
|
Topical Antimicrobial Drug Products For Over-The-Counter Human Use |
| Part 335
|
Antidiarrheal Drug Products For Over-The-Counter Human Use |
| Part 336
|
Antiemetic Drug Products For Over-The-Counter Human Use |
| Part 338
|
Nighttime Sleep-Aid Drug Products For Over-The-Counter Human Use |
| Part 340
|
Stimulant Drug Products For Over-The-Counter Human Use |
| Part 341
|
Cold, Cough, Allergy, Bronchodilator, And Antiasthmatic Drug Products For Over-The-Counter Human Use |
| Part 343
|
Internal Analgesic, Antipyretic, And Antirheumatic Drug Products For Over-The-Counter Human Use |
| Part 344
|
Topical Otic Drug Products For Over-The-Counter Human Use |
| Part 346
|
Anorectal Drug Products For Over-The-Counter Human Use |
| Part 347
|
Skin Protectant Drug Products For Over-The-Counter Human Use |
| Part 348
|
External Analgesic Drug Products For Over-The-Counter Human Use |
| Part 349
|
Ophthalmic Drug Products For Over-The-Counter Human Use |
| Part 350
|
Antiperspirant Drug Products For Over-The-Counter Human Use |
| Part 352
|
Sunscreen Drug Products For Over-The-Counter Human Use [Stayed Indefinitely] |
| Part 355
|
Anticaries Drug Products For Over-The-Counter Human Use |
| Part 357
|
Miscellaneous Internal Drug Products For Over-The-Counter Human Use |
| Part 358
|
Miscellaneous External Drug Products For Over-The-Counter Human Use |
| Part 361
|
Prescription Drugs For Human Use Generally Recognized As Safe And Effective And Not Misbranded: Drugs Used In Research |
| Part 369
|
Interpretative Statements Re Warnings On Drugs And Devices For Over-The-Counter Sale |
| Part 500
|
General |
| Part 501
|
Animal Food Labeling |
| Part 502
|
Common Or Usual Names For Nonstandardized Animal Foods |
| Part 509
|
Unavoidable Contaminants In Animal Food And Food-Packaging Material |
| Part 510
|
New Animal Drugs |
| Part 511
|
New Animal Drugs For Investigational Use |
| Part 514
|
New Animal Drug Applications |
| Part 515
|
Medicated Feed Mill License |
| Part 516
|
New Animal Drugs For Minor Use And Minor Species |
| Part 520
|
Oral Dosage Form New Animal Drugs |
| Part 522
|
Implantation Or Injectable Dosage Form New Animal Drugs |
| Part 524
|
Ophthalmic And Topical Dosage Form New Animal Drugs |
| Part 526
|
Intramammary Dosage Form New Animal Drugs |
| Part 528
|
New Animal Drugs In Genetically Engineered Animals |
| Part 529
|
Certain Other Dosage Form New Animal Drugs |
| Part 530
|
Extralabel Drug Use In Animals |
| Part 556
|
Tolerances For Residues Of New Animal Drugs In Food |
| Part 558
|
New Animal Drugs For Use In Animal Feeds |
| Part 564
|
|
| Part 570
|
Food Additives |
| Part 571
|
Food Additive Petitions |
| Part 573
|
Food Additives Permitted In Feed And Drinking Water Of Animals |
| Part 579
|
Irradiation In The Production, Processing, And Handling Of Animal Feed And Pet Food |
| Part 582
|
Substances Generally Recognized As Safe |
| Part 584
|
Food Substances Affirmed As Generally Recognized As Safe In Feed And Drinking Water Of Animals |
| Part 589
|
Substances Prohibited From Use In Animal Food Or Feed |
| Part 600
|
Biological Products: General |
| Part 601
|
Licensing |
| Part 606
|
Current Good Manufacturing Practice For Blood And Blood Components |
| Part 607
|
Establishment Registration And Product Listing For Manufacturers Of Human Blood And Blood Products |
| Part 610
|
General Biological Products Standards |
| Part 630
|
General Requirements For Blood, Blood Components, And Blood Derivatives |
| Part 640
|
Additional Standards For Human Blood And Blood Products |
| Part 660
|
Additional Standards For Diagnostic Substances For Laboratory Tests |
| Part 680
|
Additional Standards For Miscellaneous Products |
| Part 700
|
General |
| Part 701
|
Cosmetic Labeling |
| Part 710
|
Voluntary Registration Of Cosmetic Product Establishments |
| Part 720
|
Voluntary Filing Of Cosmetic Product Ingredient Composition Statements |
| Part 740
|
Cosmetic Product Warning Statements |
| Part 800
|
General |
| Part 801
|
Labeling |
| Part 803
|
Medical Device Reporting; (Eff. Until 8-14-15) |
| Part 803
|
Medical Device Reporting (Eff. 8-14-15) |
| Part 806
|
Medical Devices; Reports Of Corrections And Removals |
| Part 807
|
Establishment Registration And Device Listing For Manufacturers And Initial Importers Of Devices |
| Part 808
|
Exemptions From Federal Preemption Of State And Local Medical Device Requirements |
| Part 809
|
In Vitro Diagnostic Products For Human Use |
| Part 810
|
Medical Device Recall Authority |
| Part 812
|
Investigational Device Exemptions |
| Part 813
|
|
| Part 814
|
Premarket Approval Of Medical Devices |
| Part 820
|
Quality System Regulation |
| Part 821
|
Medical Device Tracking Requirements |
| Part 822
|
Postmarket Surveillance |
| Part 830
|
Unique Device Identification |
| Part 860
|
Medical Device Classification Procedures |
| Part 861
|
Procedures For Performance Standards Development |
| Part 862
|
Clinical Chemistry And Clinical Toxicology Devices |
| Part 864
|
Hematology And Pathology Devices |
| Part 866
|
Immunology And Microbiology Devices |
| Part 868
|
Anesthesiology Devices |
| Part 870
|
Cardiovascular Devices |
| Part 872
|
Dental Devices |
| Part 874
|
Ear, Nose, And Throat Devices |
| Part 876
|
Gastroenterology-Urology Devices |
| Part 878
|
General And Plastic Surgery Devices |
| Part 880
|
General Hospital And Personal Use Devices |
| Part 882
|
Neurological Devices |
| Part 884
|
Obstetrical And Gynecological Devices |
| Part 886
|
Ophthalmic Devices |
| Part 888
|
Orthopedic Devices |
| Part 890
|
Physical Medicine Devices |
| Part 892
|
Radiology Devices |
| Part 895
|
Banned Devices |
| Part 898
|
Performance Standard For Electrode Lead Wires And Patient Cables |
| Part 900
|
Mammography |
| Part 1000
|
General |
| Part 1002
|
Records And Reports |
| Part 1003
|
Notification Of Defects Or Failure To Comply |
| Part 1004
|
Repurchase, Repairs, Or Replacement Of Electronic Products |
| Part 1005
|
Importation Of Electronic Products |
| Part 1010
|
Performance Standards For Electronic Products: General |
| Part 1020
|
Performance Standards For Ionizing Radiation Emitting Products |
| Part 1030
|
Performance Standards For Microwave And Radio Frequency Emitting Products |
| Part 1040
|
Performance Standards For Light-Emitting Products |
| Part 1050
|
Performance Standards For Sonic, Infrasonic, And Ultrasonic Radiation-Emitting Products |
| Part 1107
|
Establishment Registration, Product Listing, And Substantial Equivalence Reports |
| Part 1140
|
Cigarettes And Smokeless Tobacco |
| Part 1141
|
Cigarette Package And Advertising Warnings |
| Part 1150
|
User Fees |
| Part 1210
|
Regulations Under The Federal Import Milk Act |
| Part 1230
|
Regulations Under The Federal Caustic Poison Act |
| Part 1240
|
Control Of Communicable Diseases |
| Part 1250
|
Interstate Conveyance Sanitation |
| Part 1270
|
Human Tissue Intended For Transplantation |
| Part 1271
|
Human Cells, Tissues, And Cellular And Tissue-Based Products |
| Part 1300
|
Definitions |
| Part 1301
|
Registration Of Manufacturers, Distributors, And Dispensers Of Controlled Substances |
| Part 1302
|
Labeling And Packaging Requirements For Controlled Substances |
| Part 1303
|
Quotas |
| Part 1304
|
Records And Reports Of Registrants |
| Part 1305
|
Orders For Schedule I And Ii Controlled Substances |
| Part 1306
|
Prescriptions |
| Part 1307
|
Miscellaneous |
| Part 1308
|
Schedules Of Controlled Substances |
| Part 1309
|
Registration Of Manufacturers, Distributors, Importers And Exporters Of List I Chemicals |
| Part 1310
|
Records And Reports Of Listed Chemicals And Certain Machines |
| Part 1311
|
Requirements For Electronic Orders And Prescriptions |
| Part 1312
|
Importation And Exportation Of Controlled Substances |
| Part 1313
|
Importation And Exportation Of List I And List Ii Chemicals |
| Part 1314
|
Retail Sale Of Scheduled Listed Chemical Products |
| Part 1315
|
Importation And Production Quotas For Ephedrine, Pseudoephedrine, And Phenylpropanolamine |
| Part 1316
|
Administrative Functions, Practices, And Procedures |
| Part 1317
|
Disposal |
| Part 1321
|
Dea Mailing Addresses |
| Part 1400
|
|
| Part 1401
|
Public Availability Of Information |
| Part 1402
|
Mandatory Declassification Review |