Orkla Health AS

1 record, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• DIETARYING1 refused line

  Dietary ingredients not listed

  The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.

• 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).

• 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.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

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

Questions about Orkla Health AS

Is Orkla Health AS on an FDA import alert?

No listing for Orkla Health AS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Norway page.

Has FDA refused shipments from Orkla Health AS?

Yes. FDA refused 1 shipment line from Orkla Health AS on October 2, 2020. The most recent, on October 2, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).

Why did FDA refuse Orkla Health AS's shipments?

The most frequent charges are DIETARYING (dietary ingredients not listed, 1 line) and LABELING (fair packaging and labeling act, 1 line).

What is Orkla Health AS's FEI number?

Orkla Health AS's FDA Establishment Identifier (FEI) is 3011300657.