FDA notice: comment request on animal food additive information collections
A December 2024 FDA notice invites 60 days of public comment on proposed information collections about animal food additives, petitions, investigational file exemptions and label declarations. [1]
Automatic summary · not editorially reviewed
The key findings
The source at a glance
- Jurisdiction
- US
- Authority
- Health and Human Services Department; Food and Drug Administration
- Document type
- Notice
- Record type / format
- Notice
- Scope / context
- Proposed FDA information collections on food additives for animal food, food additive petitions, investigational file exemptions and color additive declarations on animal food labels.
- Summary based on
- Official regulatory document
- Original publication
- December 19, 2024
FDA notice on animal food additive collections
This is a United States notice from the Health and Human Services Department and the Food and Drug Administration, published on 19 December 2024. Under the Paperwork Reduction Act of 1995, federal agencies must publish a Federal Register notice for each proposed information collection, including extensions, and allow 60 days for public comment. This notice solicits comments on the information collection provisions tied to food additives intended for use in animal food, food additive petitions, investigational food additive file exemptions and declaration of color additives on animal food labels.
Supporting source [1]
Comment window and informational web rendition
The notice opens a 60-day comment period on the proposed collection. The supplied web/API rendition is described as an informational resource, not the official legal edition. Readers are directed to verify the linked official PDF on GovInfo and any later amendments before relying on legal requirements. The source states that a proposed rule or notice is not a final rule, and that a publication date is not necessarily an effective date.
Supporting source [1]
Scope of this notice record
The supplied material is the agency abstract and metadata, not the full document. It does not determine a product's compliance or current legal status, and it is not a determination of current law. The documented subject is the proposed information collection itself, not patients or a clinical population. No biological aging topic is covered by this regulatory record.
Supporting source [1]
How to interpret this
Document summary; not a determination of current law. Based only on the agency abstract and metadata; the full document was not reviewed. The web/API rendition is informational, not the official legal edition; verify the linked official PDF on GovInfo and later amendments. A notice is not a final rule, and a publication date is not necessarily an effective date.
Based on the cited official document. Its jurisdiction, document type and effective date matter; a proposal or notice is not a rule already in force.
Source & supporting passages
Health and Human Services Department; Food and Drug Administration · federalregister.gov · December 19, 2024