Fabrica De Dulces Lovi, S.A. De C.V.

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

Refusal charges, in plain English

• 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.

• INCONSPICU1 refused line

  Required information not conspicuous

  Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

• 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.

Questions about Fabrica De Dulces Lovi, S.A. De C.V.

Is Fabrica De Dulces Lovi, S.A. De C.V. on an FDA import alert?

Yes. As of October 26, 2026, Fabrica De Dulces Lovi, S.A. De C.V. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for molachos fruit flavored powder candy; powder candy; FDA published the listing on January 22, 2010.

Has FDA refused shipments from Fabrica De Dulces Lovi, S.A. De C.V.?

Yes. FDA refused 2 shipment lines from Fabrica De Dulces Lovi, S.A. De C.V. between December 9, 2023 and August 6, 2026. The most recent, on August 6, 2026, was subtropical and tropical fruit, dried or paste, n.e.c., charged as LABELING (fair packaging and labeling act).

Why did FDA refuse Fabrica De Dulces Lovi, S.A. De C.V.'s shipments?

The most frequent charges are NUTRIT LBL (nutrition information missing from label, 2 lines) and INCONSPICU (required information not conspicuous, 1 line).

What is Fabrica De Dulces Lovi, S.A. De C.V.'s FEI number?

Fabrica De Dulces Lovi, S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3002788539.

Can shipments from Fabrica De Dulces Lovi, S.A. De C.V. still enter the U.S.?

Shipments of molachos fruit flavored powder candy; powder candy from Fabrica De Dulces Lovi, S.A. De C.V. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).