Concept Nutrition, Inc.

07/22/2026

The Food and Drug Administration (FDA or we) is issuing a final rule to amend the standard of identity for pasteurized orange juice by lowering the minimum orange juice soluble solids content from 10.5[deg] to 10[deg] Brix and permitting up to 15 percent Citrus reticulata juice or Citrus...

07/17/2026

https://www.federalregister.gov/documents/2026/07/17/2026-14438/agency-information-collection-activities-proposed-collection-comment-request-infant-formula

The Food and Drug Administration (FDA or the Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning...

07/02/2026

Today is "Made in USA" day

Dietary supplement brands face stricter rules on "Made in USA" claims, with new FTC enforcement priorities. Here's how to avoid action.

03/31/2026

FDA’s Office of Dietary Supplement Programs (ODSP) invites stakeholders to participate in a public meeting to discuss the evolving landscape of dietary suppl...

03/31/2026

The U.S. Food and Drug Administration is issuing a Request for Information today on a potential update to the acceptable market name for eighteen species of Sebastes, commonly known as rockfish.

03/25/2026

Consumers often find marketing claims such as, raised without antibiotics, cage-free, and grass-fed on protein-based food packaging. USDA’s Agricultural Marketing Service (AMS) offers audit services that provide assurance to customers on the validity of these types of claims.
Through the USDA Process Verified Program (PVP), highly skilled AMS auditors confirm that a participating company is adhering to its own set of standards. This is a voluntary service, provided by AMS to give businesses a way to show products are in fact to the standard on their label.

Transparency from Farm to Market

03/24/2026

When you see this label, it means exactly what it says.

Born here. Raised here. Harvested here. Processed here. 🇺🇸

No shortcuts. No exceptions. No confusion.

That’s Product of USA.

🔗 www.productofusa.gov

03/17/2026

https://www.fda.gov/news-events/press-announcements/fda-takes-steps-improve-gluten-ingredient-disclosure-foods

Today, the U.S. Food and Drug Administration issued a Request for Information (RFI) regarding labeling and preventing cross-contact of gluten in packaged food.

03/06/2026

the U.S. Fish and Wildlife Service proposes to amend the definition of “shellfish” in the Code of Federal Regulations (CFR) by removing the phrase “having a shell” and adding specific taxa. This amendment would clarify that squid, cuttlefish, octopus, and other cephalopods are included within the regulatory definition of shellfish. This action is deregulatory in nature, as it reduces regulatory ambiguity, aligns the Service's regulations with current biological understanding and commercial practice, reduces regulatory burden and is within the Service's purview to amend definitions as needed.
Comments must be received or postmarked on or before April 6, 2026 and can be submitted electronically using the Federal eRulemaking Portal.

We, the U.S. Fish and Wildlife Service (Service), propose to amend the definition of "shellfish" in the Code of Federal Regulations (CFR) by removing the phrase "having a shell" and adding specific taxa. This amendment would clarify that squid, cuttlefish, octopus, and other cephalopods are...

03/03/2026

March 27, 9:00am-3pm ET; in person or virtually; in-person meeting at U.S. Food and Drug Administration Wiley Auditorium, 5001 Campus Dr, College Park, MD
FDA invites stakeholders to participate in a public meeting to discuss the evolving landscape of dietary supplement ingredients and how recent scientific and technological advances are shaping the industry; there will be presentations to provide background on:
- scope of the phrase “dietary substance for use by man to supplement the diet by increasing the total dietary intake” as used in DSHEA
- New methodologies to produce existing dietary ingredients
- Specific ingredient types, including proteins, enzymes, and microbials
will include an opportunity to provide oral comment for consideration; FDA will review input received at the public meeting and submitted to www.regulations.gov (docket number FDA-2026-N-2047) to determine next steps. Comments must be submitted on or before April 27, 2026.

The U.S. Food and Drug Administration is announcing a public meeting to be held on March 27, 2026, entitled “Exploring the Scope of Dietary Supplement Ingredie