Dark Labs

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.

• 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.

• 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.

• UNSAFE ADD1 refused line

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Dark Labs

Is Dark Labs on an FDA import alert?

Yes. As of October 25, 2026, Dark Labs is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for crack dietary supplement; FDA published the listing on March 16, 2023.

Has FDA refused shipments from Dark Labs?

Yes. FDA refused 1 shipment line from Dark Labs on March 21, 2023. The most recent, on March 21, 2023, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Dark Labs's shipments?

The most frequent charges are LABELING (fair packaging and labeling act, 1 line) and LACKS FIRM (manufacturer name and address missing, 1 line).

What is Dark Labs's FEI number?

Dark Labs's FDA Establishment Identifier (FEI) is 3026106027.

Can shipments from Dark Labs still enter the U.S.?

Shipments of crack dietary supplement from Dark Labs can be detained without physical examination under Import Alert 99-39; 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).