21 CFR Part 1230
PART 1230—REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
- PART 1230—REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter L—Regulations Under Certain Other Acts Administered by the Food and Drug Administration
- Subpart A—General Provisions
- § 1230.2 Scope of the act.
- § 1230.3 Definitions.
- Subpart B—Labeling
- § 1230.10 Placement.
- § 1230.11 Required wording.
- § 1230.12 Manufacturer; distributor.
- § 1230.13 Labeling of “poison”.
- § 1230.14 Directions for treatment.
- § 1230.15 Responsibility for labeling directions for treatment.
- § 1230.16 Exemption from labeling directions for treatment.
- Subpart C—Guaranty
- § 1230.20 General guaranty.
- § 1230.21 Specific guaranty.
- Subpart D—Administrative Procedures
- § 1230.30 Collection of samples.
- § 1230.31 Where samples may be collected.
- § 1230.32 Analyzing of samples.
- § 1230.33 Investigations.
- § 1230.34 Analysis.
- § 1230.35 Hearings.
- § 1230.36 Hearings; when not provided for.
- § 1230.37 Publication.
- Subpart E—Imports
- § 1230.40 Required label information.
- § 1230.41 Delivery of containers.
- § 1230.42 Invoices.
- § 1230.43 Enforcement.
- § 1230.44 Samples.
- § 1230.45 No violation; release.
- § 1230.46 Violation.
- § 1230.47 Rejected containers.
- § 1230.48 Relabeling of containers.
- § 1230.49 Penalties.
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