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.

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

Source: eCFR API (versioner v1 structure and full text), Office of the Federal Register, titles 7, 16, 19, 21, 29, 31, 40 and 50, up to date as of October 22, 2026; retrieved October 24, 2026. Reserved sections are not counted. Boundary rules (21 CFR 210, 211 and 1308) are not drawn.

Data table

Sections and words of rule text in each mapped part (eCFR, up to date as of October 22, 2026)
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

Mapping by EUTECNIQ from each part's scope or applicability section in eCFR (read October 24, 2026). A rule set appears under every stage where it imposes a duty.

Text version of the matrix

Where each mapped rule applies in the product lifecycle (EUTECNIQ editorial mapping)
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

Conditions simplified by EUTECNIQ from each part's applicability text in eCFR (October 24, 2026). “Check” means the part applies only in the circumstances it names.

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

19 CFR 142.4, 149.2; 21 CFR 1.279, 1.509, 1.511, 1.90, 1.94, 111.75; 7 CFR 357.2–357.4; 7 CFR 319 and 330; 50 CFR 23 and 24 (eCFR, October 22, 2026); APHIS Lacey Act phase-in, Phase VII, 89 FR 47122 (May 31, 2024).

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

21 CFR 101.93(f); FD&C Act § 201(g)(1), 21 U.S.C. 321(g)(1); FDA, “Is It a Cosmetic, a Drug, or Both?” (content current as of September 11, 2024); 21 CFR 210.1, 211.1; 40 CFR 152.15, 152.25(f); 21 CFR Part 1308.

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

Source: eCFR API versions endpoint (point-in-time record), retrieved October 24, 2026. The first version in the record is the baseline and is not counted; sections removed since then are not shown.

Data table

Dates on which at least one counted section changed, from the start of the eCFR point-in-time record (late 2016 or the part's creation) to October 22, 2026
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

21 CFR 173.210, 173.230, 173.240(a), 173.250(a), 173.255(a), 173.270(a), 173.290 (eCFR, October 22, 2026).

Data table

Residue limits in spice oleoresins
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

Federal Register documents named in the key (federalregister.gov API, retrieved October 24, 2026); Pub. L. 103-417 (1994), 111-353 (2011), 117-328 (2022), 119-37 § 780 (2025); proposed compliance-date extension, 90 FR 38084 (August 7, 2025).

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

21 CFR 10.115(d)(1); 21 CFR 101.93; FDA final NDI guidance (October 2026); National Archives, “About the e-CFR”.

“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

eCFR full text, up to date as of October 22, 2026; counts cover the scope listed in the data table of the first figure.

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

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