Dabur India

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

Refusal charges, in plain English

• UNAPPROVED16 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.

• NUTRIT LBL5 refused lines

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• UNSAFE COL2 refused lines

  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.

• FILTHY1 refused line

  Filthy, putrid or decomposed substance

  The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• USUAL NAME1 refused line

  Common or usual name missing

  The label appeared not to show the common or usual name of the food.

Questions about Dabur India

Is Dabur India on an FDA import alert?

No listing for Dabur India appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the India page.

Has FDA refused shipments from Dabur India?

Yes. FDA refused 19 shipment lines from Dabur India between March 25, 2020 and December 3, 2025. The most recent, on December 3, 2025, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Dabur India's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 16 lines) and NUTRIT LBL (nutrition information missing from label, 5 lines).

When was Dabur India last inspected by FDA?

FDA's most recent inspection of Dabur India with a final classification is dated July 20, 2022 and was classified NAI (No Action Indicated).

What is Dabur India's FEI number?

Dabur India's FDA Establishment Identifier (FEI) is 3009907990.