The food label on a package of cereal, a carton of eggs, or a bag of frozen vegetables answers to a specific federal agency. For most foods sold in the United States, the Food and Drug Administration (FDA) sets the rules. For meat, poultry, and processed egg products, the U.S. Department of Agriculture (USDA) holds the authority. These two agencies are the primary regulators, but they do not work alone. The Federal Trade Commission (FTC) oversees the advertising claims that appear outside the label, and the Alcohol and Tobacco Tax and Trade Bureau (TTB) regulates most alcoholic beverages.
Who Regulates Food Labels FDA USDA And More?
The short answer is that the FDA regulates about 80 percent of the food supply, while the USDA regulates the remaining 20 percent. The split is based on what the food contains, not where it is sold. If a product contains more than 2 percent cooked meat, more than 3 percent raw meat, or any amount of poultry or egg product, the USDA takes charge. Everything else — from dairy and produce to seafood, packaged snacks, and bottled water — falls under FDA jurisdiction.
This division matters because the two agencies enforce different labeling laws. The FDA requires a standardized Nutrition Facts panel on most packaged foods. The USDA requires the same panel on meat and poultry products but also enforces its own inspection marks and grading systems. A consumer looking at a package of chicken thighs and a box of crackers is looking at two different regulatory systems.
What Exactly Does the FDA Regulate on a Food Label?
The FDA enforces the Federal Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act. These laws give the agency authority over the information that appears on food packaging. The FDA requires the Nutrition Facts label, the ingredient list, the net quantity of contents, and the name and address of the manufacturer, packer, or distributor.
The FDA also regulates nutrient content claims and health claims. A package cannot say “low sodium” unless it meets a specific definition. It cannot say “reduces the risk of heart disease” unless the FDA has reviewed and approved that specific health claim. The agency has a formal process for evaluating these claims, and manufacturers must submit evidence before using them.
Food allergens receive special attention. The FDA requires that the nine major food allergens — milk, eggs, fish, crustacean shellfish, tree nuts, peanuts, wheat, soybeans, and sesame — be declared in plain language on the label. This rule, established under the Food Allergen Labeling and Consumer Protection Act and later expanded to include sesame, helps people with food allergies identify safe products.
What Does the USDA Control on Meat and Poultry Labels?
The USDA’s Food Safety and Inspection Service (FSIS) oversees the labeling of meat, poultry, and processed egg products. This agency has a different mandate than the FDA. Its primary job is food safety, and its labeling authority is tied to that mission.
Every meat and poultry product must carry a USDA mark of inspection before it can be sold. This mark indicates that the product was processed in a facility inspected by FSIS. The label itself must be approved by FSIS before the product goes to market. This pre-approval process is different from the FDA’s approach, where most labels do not require prior approval.
The USDA also regulates claims like “grass-fed,” “free-range,” and “organic” on meat products. Some of these claims have specific definitions, while others are more loosely defined. The USDA’s Food Safety and Inspection Service requires that labeling claims be truthful and not misleading, but it does not always verify every claim before approving a label.
How Do Other Agencies Fit Into Food Label Regulation?
Three other agencies play significant roles in food labeling, though their authority is narrower.
The Federal Trade Commission (FTC) regulates advertising, not labels. If a food company makes a claim in a television commercial, a magazine ad, or a social media post, the FTC oversees that claim. The FTC requires that advertising claims be truthful, not misleading, and backed by scientific evidence. A company cannot make a health claim in an ad that it could not legally make on its label.
The Alcohol and Tobacco Tax and Trade Bureau (TTB) regulates the labeling of most alcoholic beverages, including beer, wine, and distilled spirits. The TTB requires that alcohol labels list the product name, the alcohol content, the net contents, and the name and address of the bottler or importer. The TTB also regulates statements about the alcohol’s origin, age, and production method.
The Environmental Protection Agency (EPA) does not regulate food labels directly, but it sets tolerance levels for pesticide residues on food. These tolerances affect what can be claimed on a label. A product labeled “organic” must meet the USDA’s National Organic Program standards, which include restrictions on synthetic pesticides.
What Is the Difference Between FDA and USDA Label Approval?
The approval process is one of the biggest differences between the two agencies. For most FDA-regulated foods, the manufacturer is responsible for ensuring the label complies with the law. The FDA does not pre-approve most food labels. It conducts inspections and can take enforcement action if it finds a label that violates the law.
For USDA-regulated meat and poultry products, the label must be submitted to FSIS for approval before the product can be sold. The agency reviews the label to ensure it is truthful and not misleading. This pre-approval process is a key difference. It means that a new meat product label goes through a government review before it reaches the store shelf, while a new cereal label does not.
There is an exception to the FDA’s no-pre-approval rule. The FDA does review health claims that appear on food labels. A manufacturer that wants to make a claim about the relationship between a food and a disease must submit the claim to the FDA for review. The agency evaluates the scientific evidence and decides whether the claim is supported.
What About “Natural” and “Organic” Label Claims?
The word “natural” on a food label means different things depending on which agency regulates the product. The FDA has not formally defined “natural” for most foods, though it has a policy of not objecting to the term when the food does not contain added color, artificial flavors, or synthetic substances. The USDA has a more specific definition for meat and poultry: “natural” means the product contains no artificial ingredients and is only minimally processed.
The word “organic” is more strictly regulated. The USDA’s National Organic Program sets the standards for organic food production. A product labeled “organic” must meet these standards, which cover soil quality, animal raising practices, pest and weed control, and the use of additives. Products that meet these standards can carry the USDA Organic seal.
Consumers should understand that “natural” and “organic” are not the same thing. Organic standards are defined by federal regulation. Natural claims are less standardized and can vary by product category.
What Happens When a Food Label Is Misleading?
Enforcement differs by agency. The FDA can issue warning letters, seize products, or request a court injunction when a label violates the law. The agency can also refer cases to the Department of Justice for criminal prosecution in serious situations. The USDA can withhold inspection, which effectively stops a product from being sold, or it can require a label to be corrected.
The FTC can take action against false advertising, including claims that appear on packaging if the package is considered part of the advertising. The FTC has the authority to impose civil penalties and require corrective advertising.
Consumers also have a role. If a label appears misleading, a consumer can report it to the appropriate agency. The FDA has a reporting system for food label complaints, and the USDA’s FSIS accepts consumer comments about meat and poultry labels.
Are Food Label Regulations the Same for Imported Foods?
Imported foods must meet the same labeling requirements as domestic foods. The FDA requires that imported food labels comply with the same regulations that apply to food produced in the United States. The USDA requires that imported meat and poultry products be produced in facilities that meet U.S. safety standards and carry labels that comply with FSIS requirements.
The enforcement of these requirements can be more challenging for imported foods because the products are inspected at the border rather than at the point of production. The FDA uses a risk-based approach to screen imported foods, and the USDA requires that foreign facilities be certified as meeting U.S. standards.
Frequently Asked Questions
Does the FDA regulate all food labels?
No. The FDA regulates about 80 percent of the food supply, but the USDA regulates meat, poultry, and processed egg products.
What is the difference between FDA and USDA food labels?
The FDA regulates most packaged foods and does not pre-approve most labels, while the USDA requires pre-approval of meat and poultry labels.
Who regulates the word “organic” on food labels?
The USDA’s National Organic Program sets the standards for organic claims on all food products, including those regulated by the FDA.
Who regulates alcohol labels?
The Alcohol and Tobacco Tax and Trade Bureau (TTB) regulates the labeling of most beer, wine, and distilled spirits.

