Vivus Vita

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

Refusal charges, in plain English

• 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.

• 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 Vivus Vita

Is Vivus Vita on an FDA import alert?

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

Has FDA refused shipments from Vivus Vita?

Yes. FDA refused 1 shipment line from Vivus Vita on September 2, 2026. The most recent, on September 2, 2026, was mustard oil, refined, single ingredient, see 28o for mustard oil as a flavoring, charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Vivus Vita's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 1 line) and UNSAFE ADD (food additive unsafe under section 409, 1 line).

What is Vivus Vita's FEI number?

Vivus Vita's FDA Establishment Identifier (FEI) is 3037163469.