Barbara Sturm Molecular Cosmetic Gmbh

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

Refusal charges, in plain English

• NCONTACT8 refused lines

  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.

• UNAPPROVED3 refused lines

  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.

• 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.

• SBGINSENG1 refused line

  SBGINSENG

Questions about Barbara Sturm Molecular Cosmetic Gmbh

Is Barbara Sturm Molecular Cosmetic Gmbh on an FDA import alert?

No listing for Barbara Sturm Molecular Cosmetic Gmbh appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.

Has FDA refused shipments from Barbara Sturm Molecular Cosmetic Gmbh?

Yes. FDA refused 9 shipment lines from Barbara Sturm Molecular Cosmetic Gmbh between January 24, 2018 and December 6, 2018. The most recent, on December 6, 2018, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).

Why did FDA refuse Barbara Sturm Molecular Cosmetic Gmbh's shipments?

The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 8 lines) and UNAPPROVED (unapproved new drug, 3 lines).

What is Barbara Sturm Molecular Cosmetic Gmbh's FEI number?

Barbara Sturm Molecular Cosmetic Gmbh's FDA Establishment Identifier (FEI) is 3010937300.