Proposed Information Collections: Comment Request
As required by the Paperwork Reduction Act of 1995, we are requesting comments on 13 existing information collections (forms, recordkeeping requirements, labeling requirements, and surveys). We will include or summarize any submitted comments in our request to the Office of Management and Budget (OMB) for reapproval of the described information collections. As such, all comments are part of the public record. To comment electronically, use the comment form posted with this notice in Docket No. TTB–2026–0001 on the Regulations.gov website. To comment by postal mail, see the instructions in the notice.
See the notice for the complete list of the 13 information collections due for OMB reapproval. Among those information collections are:
- OMB No. 1513–0011, Formula and/or Process for Article Made With Specially Denatured Spirits (TTB F 5150.19);
- OMB No. 1513–0024, Report - Export Warehouse Proprietor (TTB F 5220.4);
- OMB No. 1513–0039, Distilled Spirits Plants Warehousing Records, and Monthly Report of Storage Operations (TTB REC 5110/02 and TTB F 5110.11);
- OMB No. 1513–0078, Application for Permit to Manufacture or Import Tobacco Products or Processed Tobacco or to Operate an Export Warehouse and Applications to Amend Such Permits (TTB F 5200.3, 5200.16, 5230.4 and 5230.5); and
- OMB No. 1513–0084, Labeling of Sulfites in Alcohol Beverages.
Comments on any of the 13 information collections described in this notice are due to TTB by March 31, 2026.
FDA: Virtual Public Meeting and Listening Session on Food Allergen Thresholds and Their Potential Applications
 TTB-regulated industries may find this notice of interest.
SOURCE: FDA website
AGENCY: U.S. Food and Drug Administration (FDA), Department of Health and Human Services
ACTION: Notice of public meeting and listening sessions
SUMMARY: The U.S. Food and Drug Administration (FDA) will host a virtual public meeting on food allergen thresholds and their potential applications in the United States on February 18, 2026, followed by listening sessions on February 19-20, 2026. Registration is open and the event materials are now available.
FDA: Labeling and Preventing Cross-Contact of Gluten for Packaged Foods
 TTB-regulated industries may find this notice of interest.
Labeling and Preventing Cross-Contact of Gluten for Packaged Foods; Request for Information
SOURCE: Federal Register / Vol. 91, No. 14 / Thursday, January 22, 2026
AGENCY: Food and Drug Administration, Department of Health and Human Services
ACTION: Petition for rulemaking; request for information
SUMMARY: The Food and Drug Administration received a citizen petition from Celiac Journey requesting that it act to protect consumers with celiac disease by requiring that all ingredients with gluten be listed by name in the ingredient list and by requiring cross-contact controls with gluten-containing grains. FDA is issuing this document to request comment on the issues raised in the petition and on specific questions related to these issues.
DATES: Submit either electronic or written comments and scientific data and information by March 23, 2026.
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