Dabur India Limited

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

Refusal charges, in plain English

• 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.

• UNSAFE COL1 refused line

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Dabur India Limited

Is Dabur India Limited on an FDA import alert?

No listing for Dabur India Limited 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 Dabur India Limited?

Yes. FDA refused 2 shipment lines from Dabur India Limited between January 9, 2017 and September 16, 2019. The most recent, on September 16, 2019, was pomegranate, juice, other fruit juices or concentrates, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Dabur India Limited's shipments?

The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).

When was Dabur India Limited last inspected by FDA?

FDA's most recent inspection of Dabur India Limited with a final classification is dated July 22, 2016 and was classified VAI (Voluntary Action Indicated).

What is Dabur India Limited's FEI number?

Dabur India Limited's FDA Establishment Identifier (FEI) is 3008450520.