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- 21 CFR 500.52 · Use of terms such as “tonic”, “tone”, “toner”, or “conditioner” in the labeling of preparations intended for use in or on animals.
- 21 CFR 500.55 · Exemption from certain drug-labeling requirements.
- 21 CFR 500.65 · Epinephrine injection 1:1,000 in 10-milliliter containers for emergency treatment of anaphylactoid shock in cattle, horses, sheep, and swine.
- 21 CFR 500.80 · Scope of this subpart.
- 21 CFR 500.82 · Definitions.
- 21 CFR 500.84 · Conditions for approval of the sponsored compound.
- 21 CFR 500.86 · Marker residue and target tissue.
- 21 CFR 500.88 · Regulatory method.
- 21 CFR 500.90 · Waiver of requirements.
- 21 CFR 500.92 · Implementation.
- 21 CFR 500.1410 · N-methyl-2-pyrrolidone.
- 21 CFR 501.1 · Principal display panel of package form animal food.
- 21 CFR 501.2 · Information panel of package for animal food.
- 21 CFR 501.3 · Identity labeling of animal food in package form.
- 21 CFR 501.4 · Animal food; designation of ingredients.
- 21 CFR 501.5 · Animal food; name and place of business of manufacturer, packer, or distributor.
- 21 CFR 501.8 · Labeling of animal food with number of servings.
- 21 CFR 501.15 · Animal food; prominence of required statements.
- 21 CFR 501.17 · Animal food labeling warning statements.
- 21 CFR 501.18 · Misbranding of animal food.
- 21 CFR 501.22 · Animal foods; labeling of spices, flavorings, colorings, and chemical preservatives.
- 21 CFR 501.100 · Animal food; exemptions from labeling.
- 21 CFR 501.103 · Petitions requesting exemptions from or special requirements for label declaration of ingredients.
- 21 CFR 501.105 · Declaration of net quantity of contents when exempt.
- 21 CFR 501.110 · Animal feed labeling; collective names for feed ingredients.
- 21 CFR 502.5 · General principles.
- 21 CFR 502.19 · Petitions.
- 21 CFR 507.1 · Applicability and status.
- 21 CFR 507.3 · Definitions.
- 21 CFR 507.4 · Qualifications of individuals who manufacture, process, pack, or hold animal food.
- 21 CFR 507.5 · Exemptions.
- 21 CFR 507.7 · Requirements that apply to a qualified facility.
- 21 CFR 507.10 · Applicability of subparts C and E of this part to a facility solely engaged in the storage of unexposed packaged animal food.
- 21 CFR 507.12 · Applicability of this part to the holding and distribution of human food by-products for use as animal food.
- 21 CFR 507.14 · Personnel.
- 21 CFR 507.17 · Plant and grounds.
- 21 CFR 507.19 · Sanitation.
- 21 CFR 507.20 · Water supply and plumbing.
- 21 CFR 507.22 · Equipment and utensils.
- 21 CFR 507.25 · Plant operations.
- 21 CFR 507.27 · Holding and distribution.
- 21 CFR 507.28 · Holding and distribution of human food by-products for use as animal food.
- 21 CFR 507.31 · Food safety plan.
- 21 CFR 507.33 · Hazard analysis.
- 21 CFR 507.34 · Preventive controls.
- 21 CFR 507.36 · Circumstances in which the owner, operator, or agent in charge of a manufacturing/processing facility is not required to implement a preventive control.
- 21 CFR 507.37 · Provision of assurances required under § 507.36(a)(2), (3), and (4).
- 21 CFR 507.38 · Recall plan.
- 21 CFR 507.39 · Preventive control management components.
- 21 CFR 507.40 · Monitoring.
- 21 CFR 507.42 · Corrective actions and corrections.
- 21 CFR 507.45 · Verification.
- 21 CFR 507.47 · Validation.
- 21 CFR 507.49 · Verification of implementation and effectiveness.
- 21 CFR 507.50 · Reanalysis.
- 21 CFR 507.51 · Modified requirements that apply to a facility solely engaged in the storage of unexposed packaged animal food.
- 21 CFR 507.53 · Requirements applicable to a preventive controls qualified individual and a qualified auditor.
- 21 CFR 507.55 · Implementation records required for this subpart.
- 21 CFR 507.60 · Circumstances that may lead FDA to withdraw a qualified facility exemption.
- 21 CFR 507.62 · Issuance of an order to withdraw a qualified facility exemption.
- 21 CFR 507.65 · Contents of an order to withdraw a qualified facility exemption.
- 21 CFR 507.67 · Compliance with, or appeal of, an order to withdraw a qualified facility exemption.
- 21 CFR 507.69 · Procedure for submitting an appeal.
- 21 CFR 507.71 · Procedure for requesting an informal hearing.
- 21 CFR 507.73 · Requirements applicable to an informal hearing.
- 21 CFR 507.75 · Presiding officer for an appeal and for an informal hearing.
- 21 CFR 507.77 · Timeframe for issuing a decision on an appeal.
- 21 CFR 507.80 · Revocation of an order to withdraw a qualified facility exemption.
- 21 CFR 507.83 · Final agency action.
- 21 CFR 507.85 · Reinstatement of a qualified facility exemption that was withdrawn.
- 21 CFR 507.105 · Requirement to establish and implement a supply-chain program.
- 21 CFR 507.110 · General requirements applicable to a supply-chain program.
- 21 CFR 507.115 · Responsibilities of the receiving facility.
- 21 CFR 507.120 · Using approved suppliers.
- 21 CFR 507.125 · Determining appropriate supplier verification activities (including determining the frequency of conducting the activity).
- 21 CFR 507.130 · Conducting supplier verification activities for raw materials and other ingredients.
- 21 CFR 507.135 · Onsite audit.
- 21 CFR 507.175 · Records documenting the supply-chain program.
- 21 CFR 507.200 · Records subject to the requirements of this subpart.
- 21 CFR 507.202 · General requirements applying to records.
- 21 CFR 507.206 · Additional requirements applying to the food safety plan.
- 21 CFR 507.208 · Requirements for record retention.
- 21 CFR 507.212 · Use of existing records.
- 21 CFR 507.215 · Special requirements applicable to a written assurance.
- 21 CFR 509.3 · Definitions and interpretations.
- 21 CFR 509.4 · Establishment of tolerances, regulatory limits, and action levels.
- 21 CFR 509.5 · Petitions.
- 21 CFR 509.6 · Added poisonous or deleterious substances.
- 21 CFR 509.7 · Unavoidability.
- 21 CFR 509.15 · Use of polychlorinated biphenyls (PCB's) in establishments manufacturing food-packaging materials.
- 21 CFR 509.30 · Temporary tolerances for polychlorinated biphenyls (PCB's).
- 21 CFR 510.3 · Definitions and interpretations.
- 21 CFR 510.4 · Biologics; products subject to license control.
- 21 CFR 510.7 · Consignees of new animal drugs for use in the manufacture of animal feed.
- 21 CFR 510.95 · [Reserved]
- 21 CFR 510.105 · Labeling of drugs for use in milk-producing animals.
- 21 CFR 510.106 · Labeling of antibiotic and antibiotic-containing drugs intended for use in milk-producing animals.
- 21 CFR 510.110 · Antibiotics used in food-producing animals.
- 21 CFR 510.112 · Antibiotics used in veterinary medicine and for nonmedical purposes; required data.
- 21 CFR 510.201 · Scope.