Apiario Polenectar, Ltda.

5 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• DIETARYLBL5 refused lines

  Not identified as a dietary supplement

  The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

• NCONTACT3 refused lines

  No U.S. adverse event contact on supplement label

  The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

• UNAPPROVED2 refused lines

  Unapproved new drug

  The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Apiario Polenectar, Ltda.

Is Apiario Polenectar, Ltda. on an FDA import alert?

No listing for Apiario Polenectar, Ltda. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Brazil page.

Has FDA refused shipments from Apiario Polenectar, Ltda.?

Yes. FDA refused 5 shipment lines from Apiario Polenectar, Ltda. between October 11, 2017 and January 17, 2018. The most recent, on January 17, 2018, was animal by-products and extracts, n.e.c., charged as DIETARYLBL (not identified as a dietary supplement).

Why did FDA refuse Apiario Polenectar, Ltda.'s shipments?

The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 5 lines) and NCONTACT (no u.s. adverse event contact on supplement label, 3 lines).

What is Apiario Polenectar, Ltda.'s FEI number?

Apiario Polenectar, Ltda.'s FDA Establishment Identifier (FEI) is 3003899144.