Multi Mineral Supplement

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

Refusal charges, in plain English

• UNAPPROVED3 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.

• LACKS FIRM2 refused lines

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• 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.

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Multi Mineral Supplement

Is Multi Mineral Supplement on an FDA import alert?

No listing for Multi Mineral Supplement appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.

Has FDA refused shipments from Multi Mineral Supplement?

Yes. FDA refused 3 shipment lines from Multi Mineral Supplement between April 29, 2020 and June 11, 2020. The most recent, on June 11, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LACKS FIRM (manufacturer name and address missing).

Why did FDA refuse Multi Mineral Supplement's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 3 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).

What is Multi Mineral Supplement's FEI number?

Multi Mineral Supplement's FDA Establishment Identifier (FEI) is 3015601253.