Etumax

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

Refusal charges, in plain English

• UNAPPROVED62 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.

• DIRSEXMPT3 refused lines

  DIRSEXMPT

• NUTRIT LBL2 refused lines

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• DIETARYLBL1 refused line

  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).

• LABELING1 refused line

  Fair Packaging and Labeling Act

  The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

• NCONTACT1 refused line

  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.

Questions about Etumax

Is Etumax on an FDA import alert?

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

Has FDA refused shipments from Etumax?

Yes. FDA refused 63 shipment lines from Etumax between November 16, 2016 and April 2, 2025. The most recent, on April 2, 2025, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Etumax's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 62 lines) and DIRSEXMPT (dirsexmpt, 3 lines).

What is Etumax's FEI number?

Etumax's FDA Establishment Identifier (FEI) is 3008600087.