Akwa Ugo Loveth

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

Refusal charges, in plain English

• 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).

• LACKS FIRM1 refused line

  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.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• 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).

• 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 Akwa Ugo Loveth

Is Akwa Ugo Loveth on an FDA import alert?

No listing for Akwa Ugo Loveth appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Nigeria page.

Has FDA refused shipments from Akwa Ugo Loveth?

Yes. FDA refused 1 shipment line from Akwa Ugo Loveth on July 15, 2025. The most recent, on July 15, 2025, was dietary conventional foods, n.e.c., charged as LIST INGRE (ingredients not listed).

Why did FDA refuse Akwa Ugo Loveth's shipments?

The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 1 line) and LACKS FIRM (manufacturer name and address missing, 1 line).

What is Akwa Ugo Loveth's FEI number?

Akwa Ugo Loveth's FDA Establishment Identifier (FEI) is 3031275921.