Momentum

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

Refusal charges, in plain English

• 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.

• MFR INSAN1 refused line

  Insanitary manufacturing, processing or packing

  The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

• UNAPPROVED1 refused line

  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 Momentum

Is Momentum on an FDA import alert?

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

Has FDA refused shipments from Momentum?

Yes. FDA refused 3 shipment lines from Momentum between May 4, 2022 and October 21, 2022. The most recent, on October 21, 2022, was vitamin b12 (cyanocobalamin), charged as LABELING (fair packaging and labeling act).

Why did FDA refuse Momentum's shipments?

The most frequent charges are LABELING (fair packaging and labeling act, 1 line) and MFR INSAN (insanitary manufacturing, processing or packing, 1 line).

What is Momentum's FEI number?

Momentum's FDA Establishment Identifier (FEI) is 3020783615.