Amc

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

Refusal charges, in plain English

• UNSFDIETSP94 refused lines

  Dietary ingredient without safety assurance

  The product appeared to be a dietary supplement or dietary ingredient for which there is inadequate information to provide reasonable assurance that it does not present a significant or unreasonable risk of illness or injury.

• INCONSPICU3 refused lines

  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.

• FALSE2 refused lines

  False or misleading labeling

  The labeling appeared to be false or misleading in some particular.

• DIRECTIONS1 refused line

  DIRECTIONS

• UNAPPROVED1 refused line

  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.

Questions about Amc

Is Amc on an FDA import alert?

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

Has FDA refused shipments from Amc?

Yes. FDA refused 98 shipment lines from Amc between March 27, 2017 and October 21, 2022. The most recent, on October 21, 2022, was kratom (herbal and botanical teas ii, continued), charged as UNSFDIETSP (dietary ingredient without safety assurance).

Why did FDA refuse Amc's shipments?

The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 94 lines) and INCONSPICU (required information not conspicuous, 3 lines).

What is Amc's FEI number?

Amc's FDA Establishment Identifier (FEI) is 3012986165.