CFR atlas Regulation text eCFR counts, Oct 22, 2026
Ten federal agencies write the rules a botanical ingredient meets, from field to label
An atlas of 62 rule sets in 46 parts of the Code of Federal Regulations, sized by real section and word counts from eCFR, mapped to the product lifecycle and searchable by activity.
62rule sets mapped, from 46 CFR parts
10agencies, plus DEA at the boundary
2,682sections of regulation text
1,267,428words in those sections
667days with a change since the eCFR record began in 2016
Not legal advice. An orientation map of federal regulations only. The finder simplifies each rule's applicability text; confirm what applies to a real operation with qualified counsel. EUTECNIQ is pre-operational.
Related: EPA "inert ingredients" versus food excipients (Course 12) · digital lab: Part 11 and FSMA 204
The rulebook by size
EPA's pesticide-residue part alone holds 755 of the 2,682 mapped sections, more than any FDA part
Agency group, part and subpart, sized by number of sections; select a ring to zoom in and the center to zoom outeCFR counts
Data table
| Part | Group | Scope counted | Sections | Words |
|---|---|---|---|---|
| 21 CFR 1 | FDA · 21 CFR | subparts D, E, H, I, J, L, O, R, S | 166 | 69,281 |
| 21 CFR 101 | FDA · 21 CFR | whole part | 50 | 112,647 |
| 21 CFR 11 | FDA · 21 CFR | whole part | 10 | 2,466 |
| 21 CFR 111 | FDA · 21 CFR | whole part | 84 | 15,206 |
| 21 CFR 117 | FDA · 21 CFR | whole part | 61 | 23,527 |
| 21 CFR 170 | FDA · 21 CFR | whole part | 41 | 15,487 |
| 21 CFR 172 | FDA · 21 CFR | subparts F | 11 | 5,093 |
| 21 CFR 173 | FDA · 21 CFR | subparts C | 11 | 1,373 |
| 21 CFR 182 | FDA · 21 CFR | whole part | 85 | 4,967 |
| 21 CFR 184 | FDA · 21 CFR | whole part | 215 | 61,930 |
| 21 CFR 190 | FDA · 21 CFR | whole part | 1 | 749 |
| 21 CFR 50 | FDA · 21 CFR | whole part | 15 | 7,396 |
| 21 CFR 56 | FDA · 21 CFR | whole part | 20 | 5,745 |
| 21 CFR 58 | FDA · 21 CFR | whole part | 36 | 7,460 |
| 21 CFR 7 | FDA · 21 CFR | subparts C | 10 | 2,918 |
| 21 CFR 700 | FDA · 21 CFR | whole part | 12 | 4,998 |
| 21 CFR 701 | FDA · 21 CFR | whole part | 10 | 8,154 |
| 21 CFR 740 | FDA · 21 CFR | whole part | 8 | 1,491 |
| 7 CFR 205 | USDA · 7 CFR | whole part | 87 | 38,466 |
| 7 CFR 319 | USDA · 7 CFR | whole part | 128 | 50,357 |
| 7 CFR 330 | USDA · 7 CFR | whole part | 24 | 14,922 |
| 7 CFR 355 | USDA · 7 CFR | whole part | 8 | 3,978 |
| 7 CFR 357 | USDA · 7 CFR | whole part | 4 | 1,192 |
| 7 CFR 66 | USDA · 7 CFR | whole part | 29 | 5,478 |
| 40 CFR 152 | EPA · 40 CFR | whole part | 74 | 24,580 |
| 40 CFR 180 | EPA · 40 CFR | whole part | 755 | 212,657 |
| 40 CFR 261 | EPA · 40 CFR | whole part | 83 | 116,491 |
| 40 CFR 262 | EPA · 40 CFR | whole part | 66 | 41,515 |
| 16 CFR 1700 | FTC and CPSC · 16 CFR | whole part | 8 | 11,457 |
| 16 CFR 255 | FTC and CPSC · 16 CFR | whole part | 7 | 11,330 |
| 16 CFR 260 | FTC and CPSC · 16 CFR | whole part | 17 | 9,567 |
| 16 CFR 465 | FTC and CPSC · 16 CFR | whole part | 8 | 2,256 |
| 19 CFR 113 | Trade: CBP, OFAC, FWS | whole part | 53 | 16,423 |
| 19 CFR 12 | Trade: CBP, OFAC, FWS | subject groups: Food, Drugs, and Cosmetics, Plants and Plant Products, Merchandise Produced By Convict, Merchandise Subject to Economic Sanctions | 16 | 3,751 |
| 19 CFR 134 | Trade: CBP, OFAC, FWS | whole part | 33 | 8,991 |
| 19 CFR 141 | Trade: CBP, OFAC, FWS | whole part | 69 | 26,737 |
| 19 CFR 142 | Trade: CBP, OFAC, FWS | whole part | 40 | 8,905 |
| 19 CFR 149 | Trade: CBP, OFAC, FWS | whole part | 6 | 2,639 |
| 19 CFR 152 | Trade: CBP, OFAC, FWS | whole part | 21 | 11,484 |
| 19 CFR 177 | Trade: CBP, OFAC, FWS | whole part | 25 | 11,391 |
| 31 CFR 501 | Trade: CBP, OFAC, FWS | whole part | 65 | 24,153 |
| 31 CFR 560 | Trade: CBP, OFAC, FWS | whole part | 115 | 32,365 |
| 50 CFR 17 | Trade: CBP, OFAC, FWS | subparts B, F, G | 9 | 57,190 |
| 50 CFR 23 | Trade: CBP, OFAC, FWS | whole part | 73 | 41,721 |
| 50 CFR 24 | Trade: CBP, OFAC, FWS | whole part | 4 | 931 |
| 29 CFR 1910 | OSHA · 29 CFR | sections 1910.106, 1910.119, 1910.132, 1910.134, 1910.147, 1910.307, 1910.1000, 1910.1200, 1910.1450 | 9 | 125,613 |
| Total | 46 parts | 2,682 | 1,267,428 |
Size is not importance: Part 190 has a single section, the premarket notification rule for new dietary ingredients.
Explanation, details and sources
Each leaf is a part, subpart or section of the Code of Federal Regulations that applies to some stage of a botanical ingredient business. The size of a slice is the number of sections that are not reserved, or the number of words in those sections, counted from the eCFR full-text XML. Source citations inside each section are not counted; appendices that eCFR stores as separate appendix nodes are not counted.
Some parts are counted in part only: 21 CFR Part 1 (Subparts D, E, H, I, J, L, O, R and S), Part 7 (Subpart C), Part 172 (Subpart F), Part 173 (Subpart C), 19 CFR Part 12 (four subject groups), 50 CFR Part 17 (Subparts B, F and G) and nine sections of 29 CFR Part 1910. The data table names the scope of every count.
Out of scope here: statutes (the U.S. Code), guidance documents, state rules such as California's Proposition 65 (see legal status and questions for counsel) and rules of other countries (see international market access). The National Archives describes the eCFR as “an unofficial editorial compilation of CFR material and Federal Register amendments” and not an official legal edition of the CFR; legal research should be checked against the official CFR.
Lifecycle × agency
Importing touches 21 of the 62 mapped rule sets, more than any other stage of the lifecycle
Each chip is one rule set; select a stage to isolate it, or a chip to read its one-line summaryEditorial mapping
Text version of the matrix
| Agency | Source | Import | Status | Make | Test | Label | Market | Export | Workplace |
|---|---|---|---|---|---|---|---|---|---|
| FDA | Part 1, Subpart J; Part 1, Subpart L; Part 1, Subpart S; Part 117 | Part 1, Subpart D; Part 1, Subpart E; Part 1, Subpart I; Part 1, Subpart L; Part 1, Subpart R | Part 50; Part 56; Part 58; Part 170; Part 172, Subpart F; Part 173, Subpart C; Part 182; Part 184; Part 190; Part 700 | Part 1, Subpart H; Part 111; Part 117; Part 173, Subpart C; Parts 210 and 211 | Part 1, Subpart R; Part 11; Part 58; Part 111 | Part 101; Part 701; Part 740 | Part 1, Subpart J; Part 1, Subpart O; Part 1, Subpart S; Part 7, Subpart C | Part 1, Subpart E | |
| DEA | Part 1308 (DEA) | ||||||||
| AMS | Part 205 | Part 205 | Part 205 | Part 205; Part 66 | |||||
| APHIS | Part 319; Part 330; Part 355; Part 357 | Part 355 | |||||||
| EPA | Part 180 | Part 152 | Part 180 | Part 152 | Part 261; Part 262 | ||||
| FTC | Part 255; Part 260; Part 465 | ||||||||
| CPSC | Part 1700 | ||||||||
| CBP | Part 12; Part 113; Part 134; Part 141; Part 142; Part 149; Part 152; Part 177 | Part 134 | |||||||
| OFAC | Part 501; Part 560 | Part 560 | Part 501; Part 560 | ||||||
| FWS | Part 17; Part 23 | Part 23; Part 24 | Part 17; Part 23; Part 24 | ||||||
| OSHA | § 1910.106; § 1910.119; § 1910.147; § 1910.307 | § 1910.1450 | § 1910.1200; § 1910.106; § 1910.119; § 1910.132; § 1910.134; § 1910.147; § 1910.307; § 1910.1000; § 1910.1450 |
Workplace and environmental rules from OSHA and EPA apply to any site with solvents or a laboratory, whatever the product.
Part finder
Tick what a business does and the finder lists the parts that apply and the parts to check
Which federal rules would apply to this operation?Orientation, not legal advice
Method, assumptions and limits
What it does. Each rule set carries one or more conditions written as combinations of the boxes above, taken from its scope or applicability section. A rule set is listed under “Applies” when a condition marked as applying is met, under “Check” when only a conditional one is met, and under “Boundary” when it would apply only if the product changed category.
What it does not establish. Exemptions, size thresholds, state law, contracts and the facts of a real operation are not modeled. A rule missing from the list may still apply. The finder is not legal advice.
Linking to a selection. The address bar keeps the current selection, for example ?roles=S&acts=imp,lab (finished supplements, importing, in-house laboratory); ?preset=root, us, ext or cos loads an example. Each one-line card below has its own anchor, such as #ca-p-21-111 for 21 CFR Part 111.
Worked example
A container of dried roots meets CBP, FDA and APHIS before it reaches a U.S. supplement plant
Import of a dried botanical for supplement manufacture, by ocean freight: who files what, and whenRegulation
Text version of the import sequence
- Before shipping, the importer qualifies the foreign supplier under the Foreign Supplier Verification Program (21 CFR Part 1, Subpart L); a supplement maker that tests the incoming ingredient itself follows the modified requirements of § 1.511(a).
- No later than 24 hours before the container is laden at the foreign port, the importer files the Importer Security Filing (19 CFR 149.2).
- Before arrival, FDA prior notice is submitted and confirmed: at least 8 hours before arrival by water (21 CFR 1.279).
- At entry, the broker files the CBP entry with FDA's data elements (21 CFR Part 1, Subpart D), the importer's FSVP identification (§ 1.509), a bond (19 CFR 142.4) and, if the tariff code is on APHIS's phase-in schedule, the Lacey Act plant declaration (7 CFR 357.3). APHIS has phased the declaration in by tariff code since April 1, 2009; Phase VII, from December 1, 2024, added wild ginseng roots, ephedra and Prunus africana bark (89 FR 47122). The Lacey Act definition of "plant" excludes common cultivars and common food crops (7 CFR 357.2).
- FDA reviews admissibility and may release, sample (§ 1.90) or refuse the shipment, with a hearing (§ 1.94). APHIS requirements apply when the commodity is regulated for plant pests (7 CFR 319, 330). A CITES-listed species also needs permits and a designated port (50 CFR 23, 24).
- After release, the plant tests the identity of the dietary ingredient before use (21 CFR 111.75(a)(1)).
Where required, the Lacey Act declaration names the plant's genus and species, so identity is a customs matter before a laboratory one.
Boundaries
A claim or a listed substance can move a botanical into another agency's rulebook
Four triggers that change which rules applyStatute and regulation
Text version of the boundaries
- A dietary supplement whose labeling claims to diagnose, treat, cure, mitigate or prevent a disease is regulated as a drug unless the claim is an authorized health claim (21 CFR 101.93(f)); drug CGMP is in 21 CFR Parts 210 and 211.
- A cosmetic that claims to affect the structure or a function of the body, for example to regenerate cells, is a drug as well as a cosmetic (FD&C Act § 201(g)(1)(C); FDA examples).
- A product intended to prevent, destroy, repel or mitigate pests is a pesticide and must be registered with EPA unless exempt, for example as a minimum-risk pesticide (40 CFR 152.15, 152.25(f)).
- A plant or constituent listed in the schedules of controlled substances (21 CFR Part 1308) is regulated by DEA under the Controlled Substances Act.
Claims on websites and in advertising are evidence of intended use, so a disease claim online can move a supplement into the drug rules.
How often the rules change
Species, tolerance and drug-schedule lists changed on 165 to 341 days since late 2016; the supplement CGMP rule did not change once
Each tick is a day on which at least one counted section changed, December 2016 to October 2026eCFR version history
Data table
| Part | Agency | Change dates | Latest change |
|---|---|---|---|
| 50 CFR 17 | FWS | 341 | 2026-08-20 |
| 40 CFR 180 | EPA | 198 | 2026-09-29 |
| 21 CFR 1308 | DEA | 165 | 2026-10-21 |
| 7 CFR 205 | AMS | 36 | 2025-03-21 |
| 40 CFR 261 | EPA | 24 | 2025-09-11 |
| 40 CFR 262 | EPA | 24 | 2025-09-11 |
| 29 CFR 1910 | OSHA | 20 | 2026-02-13 |
| 31 CFR 501 | OFAC | 20 | 2026-07-27 |
| 21 CFR 101 | FDA | 19 | 2025-04-28 |
| 7 CFR 319 | APHIS | 19 | 2026-10-08 |
| 31 CFR 560 | OFAC | 16 | 2026-09-30 |
| 21 CFR 1 | FDA | 15 | 2025-10-27 |
| 19 CFR 113 | CBP | 12 | 2026-08-26 |
| 19 CFR 141 | CBP | 11 | 2026-02-06 |
| 7 CFR 330 | APHIS | 7 | 2025-06-16 |
| 21 CFR 117 | FDA | 6 | 2022-10-31 |
| 21 CFR 184 | FDA | 6 | 2023-12-22 |
| 19 CFR 12 | CBP | 5 | 2022-05-19 |
| 19 CFR 149 | CBP | 5 | 2021-08-19 |
| 21 CFR 170 | FDA | 5 | 2024-05-21 |
| 19 CFR 142 | CBP | 4 | 2017-11-27 |
| 21 CFR 211 | FDA | 4 | 2025-12-18 |
| 50 CFR 23 | FWS | 4 | 2022-11-02 |
| 16 CFR 1700 | CPSC | 3 | 2024-05-20 |
| 19 CFR 134 | CBP | 3 | 2022-05-19 |
| 21 CFR 11 | FDA | 3 | 2023-03-02 |
| 7 CFR 66 | AMS | 3 | 2024-01-12 |
| 19 CFR 152 | CBP | 2 | 2017-07-19 |
| 19 CFR 177 | CBP | 2 | 2024-08-23 |
| 21 CFR 210 | FDA | 2 | 2025-12-18 |
| 21 CFR 50 | FDA | 2 | 2024-01-22 |
| 21 CFR 7 | FDA | 2 | 2023-07-14 |
| 40 CFR 152 | EPA | 2 | 2023-01-09 |
| 7 CFR 355 | APHIS | 2 | 2018-03-15 |
| 16 CFR 255 | FTC | 1 | 2023-07-26 |
| 21 CFR 172 | FDA | 1 | 2017-10-09 |
| 21 CFR 173 | FDA | 1 | 2023-03-24 |
| 21 CFR 190 | FDA | 1 | 2023-03-24 |
| 21 CFR 740 | FDA | 1 | 2023-07-14 |
| 7 CFR 357 | APHIS | 1 | 2020-03-02 |
| 16 CFR 260 | FTC | 0 | none since 2016-12-22 |
| 16 CFR 465 | FTC | 0 | none since 2024-10-21 |
| 21 CFR 111 | FDA | 0 | none since 2016-12-19 |
| 21 CFR 182 | FDA | 0 | none since 2016-11-22 |
| 21 CFR 56 | FDA | 0 | none since 2016-12-29 |
| 21 CFR 58 | FDA | 0 | none since 2016-12-29 |
| 21 CFR 700 | FDA | 0 | none since 2016-11-29 |
| 21 CFR 701 | FDA | 0 | none since 2016-11-29 |
| 50 CFR 24 | FWS | 0 | none since 2016-12-16 |
A monitoring plan would watch the fast-changing lists weekly and the slow-changing rules for proposals in the Federal Register.
Numbers in the rules
The CFR's extraction-solvent limits are written for spice oleoresins, not for supplement extracts
Residue limits for extraction solvents in spice oleoresins, 21 CFR Part 173, Subpart C (ppm)Regulation
Data table
| Solvent | Section | Limit (ppm) | Note |
|---|---|---|---|
| Isopropyl alcohol | 173.240(a) | 50 | Also 6 ppm in lemon oil; 2.0% in hops extract |
| Methyl alcohol | 173.250(a) | 50 | Also 2.2% in hops extract |
| Acetone | 173.210 | 30 | |
| Ethylene dichloride | 173.230 | 30 | Chlorinated solvents together not above 30 ppm |
| Methylene chloride | 173.255(a) | 30 | Chlorinated solvents together not above 30 ppm; also 2.2% in hops extract, 10 ppm in decaffeinated coffee |
| Trichloroethylene | 173.290 | 30 | Chlorinated solvents together not above 30 ppm; also 25 and 10 ppm in decaffeinated coffees |
| Hexane | 173.270(a) | 25 | Also 2.2% in hops extract |
For a supplement extract, residual-solvent specifications come from the firm's own Part 111 specifications and compendial references.
Explanation, details and sources
Part 173, Subpart C names the foods to which each limit applies: spice oleoresins, lemon oil, hops extract and decaffeinated coffee. None of its sections names a dietary-supplement extract. Under Part 111 the manufacturer establishes, for each component, an identity specification, the specifications needed for the purity, strength and composition of the finished supplement, and limits on contamination that may adulterate it (21 CFR 111.70(b)).
Rulemaking timeline
Thirty-two years of rulemaking, from DSHEA in 1994 to the 2026 proposal on GRAS notices
Statutes and final rules behind the atlas, by agency; the open ring is a proposalFederal Register
Most of the supplement rulebook dates from 1997–2016; since 2022 the changes have come in traceability, organic enforcement, advertising and GRAS.
Binding force
Statutes and regulations bind; FDA guidance describes the agency's current thinking and does not
Where the CFR sits among the documents that shape complianceRegulation
“Guidance documents do not establish legally enforceable rights or responsibilities” (21 CFR 10.115(d)(1)); an alternative approach must still comply with the statute and regulations.
Every part in one line
Every mapped rule set in one plain sentence, grouped by agency, with its eCFR link
The fifteen largest mapped parts by words of regulation texteCFR counts
Open a group to read each rule set's one-line summary, the provision it rests on and the lifecycle stages it touches.
FDA · 21 CFR: 26 entries
- 21 CFR Part 1, Subpart D Electronic Import EntriesLists the data FDA needs in each electronic customs entry of an FDA-regulated article.FDA · § 1.70 · Import
- 21 CFR Part 1, Subpart E Imports and ExportsFDA import sampling, hearings and relabeling of refused goods, and the records kept for certain exports.FDA · §§ 1.90–1.101 · Import, Export
- 21 CFR Part 1, Subpart H Registration of Food FacilitiesFacilities that make, process, pack or hold food for U.S. consumption register with FDA and renew every two years.FDA · §§ 1.225, 1.230 · Make
- 21 CFR Part 1, Subpart I Prior Notice of Imported FoodImported food needs prior notice to FDA: at least 2 hours before arrival by road, 4 by rail or air, 8 by water.FDA · §§ 1.277, 1.279 · Import
- 21 CFR Part 1, Subpart J Establishment, Maintenance, and Availability of RecordsKeep records of the immediate previous source and the immediate subsequent recipient of food.FDA · §§ 1.326, 1.337, 1.345 · Source, Market
- 21 CFR Part 1, Subpart L Foreign Supplier Verification Programs for Food ImportersImporters verify that foreign suppliers produce food safely; § 1.511 modifies the program for dietary supplements.FDA · §§ 1.501, 1.511 · Source, Import
- 21 CFR Part 1, Subpart O Sanitary Transportation of Human and Animal FoodShippers, loaders, carriers and receivers keep food safe during transport; § 1.900(b) lists exempt operations.FDA · § 1.900 · Market
- 21 CFR Part 1, Subpart R Laboratory Accreditation for Analyses of FoodsCertain food tests, such as tests to support admission of an import, must be run by a LAAF-accredited laboratory.FDA · § 1.1107 · Test, Import
- 21 CFR Part 1, Subpart S Additional Traceability Records for Certain FoodsExtra traceability records for foods on FDA's Food Traceability List, which names fresh herbs; dried herbs, extracts and supplements are not named.FDA · § 1.1300; FDA Food Traceability List · Source, MarketSee also Digital lab: FSMA 204 tracking events and data elements
- 21 CFR Part 7, Subpart C Enforcement PolicyFDA's recall policy: recalls are voluntary actions, classified by health hazard, with a recall strategy.FDA · §§ 7.40–7.42 · Market
- 21 CFR Part 11 Electronic Records; Electronic SignaturesElectronic records and signatures that meet FDA record rules must be trustworthy, reliable and equivalent to paper.FDA · § 11.1 · TestSee also Digital lab: Part 11 and ALCOA+ controls
- 21 CFR Part 50 Protection of Human SubjectsInformed consent of human subjects in FDA-regulated clinical investigations.FDA · § 50.1 · Status
- 21 CFR Part 56 Institutional Review BoardsInstitutional review boards that review FDA-regulated clinical investigations.FDA · § 56.101 · Status
- 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory StudiesGood laboratory practice for nonclinical studies supporting the FDA submissions listed in § 58.3; NDINs are not listed.FDA · §§ 58.1, 58.3 · Status, Test
- 21 CFR Part 101 Food LabelingFood labels: Supplement Facts (§ 101.36), health claims (§ 101.14) and structure/function statements (§ 101.93).FDA · §§ 101.36, 101.14, 101.93 · Label
- 21 CFR Part 111 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary SupplementsCGMP for anyone who makes, packages, labels or holds a dietary supplement, including identity tests of dietary ingredients.FDA · §§ 111.1, 111.75 · Make, Test
- 21 CFR Part 117 Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human FoodCGMP, hazard analysis and preventive controls for human food, including dietary ingredients.FDA · §§ 117.1, 117.5 · Source, Make
- 21 CFR Part 170 Food AdditivesFood additive rules and the GRAS notice procedure (Subpart E); a 2026 proposal would make GRAS notices mandatory.FDA · §§ 170.30, 170.205 · Status
- 21 CFR Part 172, Subpart F Food Additives Permitted for Direct Addition to Food for Human ConsumptionNatural flavoring substances and adjuvants, many of them plants, with their conditions of use (§ 172.510).FDA · § 172.510 · Status
- 21 CFR Part 173, Subpart C Secondary Direct Food Additives Permitted in Food for Human ConsumptionResidue limits for extraction solvents in named foods, such as hexane at 25 ppm in spice oleoresins.FDA · §§ 173.210–173.290 · Status, Make
- 21 CFR Part 182 Substances Generally Recognized as SafeSubstances generally recognized as safe, including spices (§ 182.10) and essential oils and natural extractives (§ 182.20).FDA · §§ 182.10, 182.20 · Status
- 21 CFR Part 184 Direct Food Substances Affirmed as Generally Recognized as SafeIngredients FDA has affirmed as GRAS for the purposes and conditions stated in each section.FDA · § 184.1 · Status
- 21 CFR Part 190 Dietary SupplementsA new dietary ingredient needs notification to FDA at least 75 days before marketing, unless the food-supply exception applies.FDA · § 190.6 · Status
- 21 CFR Part 700 GeneralGeneral cosmetic rules, including ingredients prohibited in cosmetics such as methylene chloride (§ 700.19).FDA · §§ 700.11–700.35 · Status
- 21 CFR Part 701 Cosmetic LabelingCosmetic labeling, including the designation of ingredients (§ 701.3).FDA · § 701.3 · Label
- 21 CFR Part 740 Cosmetic Product Warning StatementsWarning statements required on certain cosmetic products.FDA · Part 740 · Label
USDA · 7 CFR: 6 entries
- 7 CFR Part 205 National Organic ProgramOrganic production, handling and labeling; operations selling organic products are certified unless exempt (§ 205.100).AMS · §§ 205.100, 205.273 · Source, Import, Make, Label
- 7 CFR Part 66 National Bioengineered Food Disclosure StandardBioengineered food disclosure on labels; the part's definitions and exemptions decide coverage.AMS · §§ 66.1, 66.3 · Label
- 7 CFR Part 319 Foreign Quarantine NoticesConditions for importing plants and plant products that can carry pests; they depend on the commodity and origin.APHIS · Part 319 · Import
- 7 CFR Part 330 Federal Plant Pest Regulations; General; Plant Pests, Biological Control Organisms, and Associated Articles; GarbageRestrictions on moving plant pests, biological control organisms and associated articles, and on garbage.APHIS · § 330.200 · Import
- 7 CFR Part 355 Endangered Species Regulations Concerning Terrestrial PlantsAPHIS enforcement at ports for trade in terrestrial plants protected under the ESA and CITES.APHIS · § 355.1 · Import, Export
- 7 CFR Part 357 Control of Illegally Taken PlantsLacey Act plant declaration: scientific name, value, quantity and country where the plant was taken (§ 357.3).APHIS · §§ 357.2–357.4; APHIS phase-in schedule · Import
EPA · 40 CFR: 4 entries
- 40 CFR Part 152 Pesticide Registration and Classification ProceduresA product intended to prevent, destroy, repel or mitigate pests is a pesticide; minimum-risk products are exempt (§ 152.25(f)).EPA · §§ 152.15, 152.25 · Status, Label
- 40 CFR Part 180 Tolerances and Exemptions for Pesticide Chemical Residues in FoodTolerances and exemptions for pesticide residues in food; inert-ingredient exemptions are in §§ 180.910–180.960.EPA · Part 180 · Source, Test
- 40 CFR Part 261 Identification and Listing of Hazardous WasteWhich wastes are hazardous: ignitable wastes (§ 261.21) and listed wastes such as spent solvents (§ 261.31).EPA · §§ 261.21, 261.31 · Workplace
- 40 CFR Part 262 Standards Applicable to Generators of Hazardous WasteDuties of hazardous-waste generators, scaled by generator category.EPA · § 262.10 · Workplace
FTC and CPSC · 16 CFR: 4 entries
- 16 CFR Part 255 Guides Concerning Use of Endorsements and Testimonials in AdvertisingHow the FTC applies Section 5 of the FTC Act to endorsements and testimonials in advertising.FTC · § 255.0 · Market
- 16 CFR Part 260 Guides for the Use of Environmental Marketing ClaimsThe Green Guides: the FTC's views on environmental marketing claims.FTC · § 260.1 · Market
- 16 CFR Part 465 Rule on the Use of Consumer Reviews and TestimonialsBans fake reviews and testimonials, buying sentiment-conditioned reviews, insider reviews and review suppression.FTC · §§ 465.2–465.8 · Market
- 16 CFR Part 1700 Poison Prevention PackagingChild-resistant packaging, including supplements with 250 mg or more elemental iron per package (§ 1700.14(a)(13)).CPSC · § 1700.14 · Label
Trade: CBP, OFAC, FWS: 13 entries
- 19 CFR Part 12 (selected subject groups) Special Classes of MerchandiseCBP rules for FDA-regulated goods (§ 12.1), plants, goods made with forced labor, and goods under sanctions.CBP · § 12.1 · Import
- 19 CFR Part 113 CBP BondsCustoms bonds that secure payment of duties and compliance with import rules.CBP · Part 113 · Import
- 19 CFR Part 134 Country of Origin MarkingCountry-of-origin marking of imported articles or their containers (§ 134.11).CBP · § 134.11 · Import, Label
- 19 CFR Part 141 Entry of MerchandiseEntry of merchandise: liability for duties, who may enter, invoices, duty deposits and release.CBP · Part 141 · Import
- 19 CFR Part 142 Entry ProcessThe entry process: entry documents, entry summary, immediate delivery and line release.CBP · Part 142 · Import
- 19 CFR Part 149 Importer Security FilingImporter Security Filing for ocean cargo; core data due 24 hours before loading at the foreign port.CBP · § 149.2 · Import
- 19 CFR Part 152 Classification and Appraisement of MerchandiseTariff classification and customs valuation of imported goods.CBP · Part 152 · Import
- 19 CFR Part 177 Administrative RulingsBinding advance rulings from CBP, for example on tariff classification.CBP · Part 177 · Import
- 31 CFR Part 501 Reporting, Procedures and Penalties RegulationsStandard reporting, recordkeeping and license-application procedures for OFAC sanctions programs.OFAC · Part 501 · Source, Export
- 31 CFR Part 560 Iranian Transactions and Sanctions RegulationsIranian Transactions and Sanctions Regulations: importing Iranian-origin goods is prohibited unless authorized (§ 560.201).OFAC · §§ 560.201, 560.204 · Source, Import, Export
- 50 CFR Part 17, Subparts B, F, G Endangered and Threatened Wildlife and PlantsLists of endangered and threatened plants (§ 17.12) and the prohibitions that protect them.FWS · §§ 17.12, 17.61, 17.71 · Source, Export
- 50 CFR Part 23 Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES)CITES permits and certificates for trade in listed species, including American ginseng exports (§ 23.68).FWS · §§ 23.1, 23.68 · Source, Import, Export
- 50 CFR Part 24 Importation and Exportation of PlantsDesignated ports for importing, exporting and re-exporting plants.FWS · § 24.1 · Import, Export
OSHA · 29 CFR: 9 entries
- 29 CFR 1910.1200 Hazard communication.Hazard communication: hazard classification, labels, safety data sheets and worker training.OSHA · § 1910.1200(b) · Workplace
- 29 CFR 1910.106 Flammable liquids.Storage and handling of flammable liquids, such as ethanol and hexane used in extraction.OSHA · § 1910.106 · Make, Workplace
- 29 CFR 1910.119 Process safety management of highly hazardous chemicals.Process safety management, triggered for example by 10,000 lb of a flammable liquid with flash point below 100 °F in one process.OSHA · § 1910.119(a) · Make, Workplace
- 29 CFR 1910.132 General requirements.Workplace hazard assessment and personal protective equipment.OSHA · § 1910.132 · Workplace
- 29 CFR 1910.134 Respiratory protection.Respiratory protection programs where respirators are needed.OSHA · § 1910.134 · Workplace
- 29 CFR 1910.147 The control of hazardous energy (lockout/tagout).Lockout/tagout of hazardous energy during servicing and maintenance of machines.OSHA · § 1910.147 · Make, Workplace
- 29 CFR 1910.307 Hazardous (classified) locations.Electrical equipment in hazardous (classified) locations, such as rooms with flammable vapors.OSHA · § 1910.307 · Make, Workplace
- 29 CFR 1910.1000 Air contaminants.Permissible exposure limits for air contaminants, such as solvent vapors.OSHA · § 1910.1000 · Workplace
- 29 CFR 1910.1450 Occupational exposure to hazardous chemicals in laboratories.Chemical hygiene plan and exposure controls for laboratory use of hazardous chemicals.OSHA · § 1910.1450(a) · Test, Workplace
Boundary rules: 2 entries
- 21 CFR Part 210 and Part 211 and 21 CFR Part 211 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General; Current Good Manufacturing Practice for Finished PharmaceuticalsDrug CGMP. Applies when a product is a drug, for example because its labeling makes disease claims.FDA · §§ 210.1, 211.1 · Make
- 21 CFR Part 1308 Schedules of Controlled SubstancesSchedules of controlled substances. A listed plant or constituent is regulated by DEA, not as a supplement ingredient.DEA · Part 1308 · Status
Mapping the rules for a specific ingredient?
EUTECNIQ would scope the pathway with qualified regulatory counsel.